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Fat stem cells or bone marrow stem cells? – Dr. Marc …

September 16th, 2019 12:44 pm

If you are suffering from osteoarthritic pain and are researching alternatives to joint replacement or for help in relieving continued pain after joint replacement you will come upon information comparing the use of bone marrow derived stem cells and adipose or fat derived stem cells in aiding your situation.

In my office I choose to use bone marrow-derived stem cells because I find that we can achieve both success in the patients expectations and the goals of the treatment of Stem Cell Therapy, which can be accomplished best and simply by harnessing bone marrow stem cells.

We do not use adipose (fat) stem cells since it is more traumatic for the patient. In addition to breaking up fat tissue with a long trocar, a thick needle has to be used for the injections. In short, adipose procedures are not liked by patients.

Bone Marrow Aspiration (harvesting the stem cells from bone marrow) takes about a minute once I locate the specific area to aspirate, is basically painless for most patients after a lidocaine injection, and can be injected with very small needle. In addition, when we use bone marrow, we are injecting both platelets (PRP) from the bone marrow and stem cells from the bone marrow, in essence two treatments instead of one.

As we discuss these techniques it is important to understand that medicine is a practice and an evolving one. Medicine is also a technology and the technology is ever advancing. Tomorrow Stem Cell Therapy may evolve into something altogether different and we may find new techniques that achieve the results we are looking for.

Researchers have evaluated the effectiveness of Stem Cell Therapy and tissue engineering for treating osteoarthritis. Both bone marrow and adipose-derived stem cells have the potential to provide a permanent biological solution.

One must be careful in analyzing studies.

One study I read suggests that there are more stem cells in adipose than bone marrow. But we are not sure that the number of cells is important, since stem cells divide logarithmically inside the body. And the following studies show that bone marrow stem cells are more effective than adipose stem cells.

A paper from 2016published by doctors at the Department of Orthopedics, Georgia Regents University compiled the following findings:

This clinical study from the Guilin Medical College in China, demonstrated bone-marrow-MSCs to have greater in vivo chondrogenic potential than periosteum, synovium, adipose, and muscle MSCs in this research from the Department of Orthopaedics, the Affiliated Hospital of Guilin Medical College, Guilin, China.6

In an editorial in the January 2016 issue of the Journal of Arthroscopic and Related Surgery, Associate Editor Merrick J. Wetzler, M.D., wrote: Harvesting of the ADSCs [fat stem cells] does require an additional procedure, and the cost-effectiveness of the procedure is still under investigation, but as researchers stated in their editorials in 2012 and 2013, We are believers in Stem Cell Therapy and Stem cells have substantial potential to allow 21st century physicians and surgeons to achieve unprecedented tissue healing and repair.

We do believe that it is only a matter of time before the harvesting and growth of stem cells will become cost-effective and commercially available and will be added to our treatment options for restoration of articular cartilage.

That is a good endorsement from surgeons however, as Dr. Wetzler noted, there is an added cost of the stem cell procedure using adipose (fat) stem cells, along with the more complex harvesting procedure involved in obtaining the fat cells.

Nevertheless, there is more research pending on the value of stem cells from bone marrow vs fat, and other doctors in the field have not concurred on the best modality. In time, studies will most likely provide the answer. And since the field is fairly new, much more exploration is required.

1 Shapiro SA, Kazmerchak SE, Heckman MG, Zubair AC, OConnor MI. A Prospective, Single-Blind, Placebo-Controlled Trial of Bone Marrow Aspirate Concentrate for Knee Osteoarthritis. Am J Sports Med. 2017 Jan;45(1):82-90. doi: 10.1177/0363546516662455. Epub 2016 Sep 30.

2: Jakobsen RB, Shahdadfar A, Reinholt FP, Brinchmann JE. Chondrogenesis in a hyaluronic acid scaffold: comparison between chondrocytes and MSC from bone marrow and adipose tissue. Knee Surg Sports Traumatol Arthrosc. 2010 Oct;18(10):1407-16. doi: 10.1007/s00167-009-1017-4. Epub 2009 Dec 18. Erratum in:Knee Surg Sports Traumatol Arthrosc. 2014 Jul;22(7):1711-4.

3. Shafiee A, Seyedjafari E, Soleimani M, Ahmadbeigi N, Dinarvand P, Ghaemi N. A comparison between osteogenic differentiation of human unrestricted somatic stem cells and mesenchymal stem cells from bone marrow and adipose tissue. Biotechnol Lett. 2011 Jun;33(6):1257-64. doi: 10.1007/s10529-011-0541-8. Epub 2011 Feb 2.

4. Frisbie DD, Kisiday JD, Kawcak CE, Werpy NM, McIlwraith CW. Evaluation of adipose-derived stromal vascular fraction or bone marrow-derived mesenchymal stem cells for treatment of osteoarthritis. J Orthop Res. 2009 Dec;27(12):1675-80. doi: 10.1002/jor.20933. Colorado State University

5 Burke, J., Hunter, M., Kolhe, R., Isales, C., Hamrick, M., & Fulzele, S. (2016). Therapeutic potential of mesenchymal stem cell based therapy for osteoarthritis.Clinical and Translational Medicine,5, 27. http://doi.org/10.1186/s40169-016-0112-7

6. Li Q, Tang J, Wang R, Bei C, Xin L, Zeng Y, Tang X. Comparing the chondrogenic potential in vivo of autogeneic mesenchymal stem cells derived from different tissues. Artif Cells Blood Substit Immobil Biotechnol. 2011 Feb;39(1):31-8. doi: 10.3109/10731191003776769. Epub 2010 Nov 30. PubMed PMID: 21117872. Guillen China

7 Niemeyer P, Fechner K, Milz S, Richter W, Suedkamp NP, Mehlhorn AT, Pearce S, Kasten P. Comparison of mesenchymal stem cells from bone marrow and adipose tissue for bone regeneration in a critical size defect of the sheep tibia and the influence of platelet-rich plasma. Biomaterials. 2010 May;31(13):3572-9.

8 Vidal MA, Robinson SO, Lopez MJ, Paulsen DB, Borkhsenious O, Johnson JR, Moore RM, Gimble JM. Comparison of chondrogenic potential in equine mesenchymal stromal cells derived from adipose tissue and bone marrow. Vet Surg. 2008 Dec;37(8):713-24. doi: 10.1111/j.1532-950X.2008.00462.x. PubMed PMID: 19121166;PubMed Central PMCID: PMC2746327.

9 Chang YH, Liu HW, Wu KC, Ding DC. Mesenchymal stem cells and their clinical applications in osteoarthritis. Cell Transplant. 2015 Dec 18. [Epub ahead of print.]

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What Is Preventive Medicine? A Look at Proactive Providers

September 15th, 2019 6:42 pm

We go through life day by day, each with our own set schedules and habits. When things go wrong, we get into accidents, or we fall ill, we rely on trusted doctors and health care professionals to help us recover.

Thats how much of health care works responsive action taken to treat a sickness or disease already underway.

But what if we could avoid getting sick in the first place? Thats what preventive medicine is all about. Most areas of medicine narrowly focus on a single age group, ailment, or body part. But preventive medicine does not have these boundaries, making it a very broad field.

But what is preventive medicine? And why is it so important? Keep reading to learn more about the field of preventive medicine and why its reach spans not just individual patients, but scores of communities and populations.

Preventive medicine is exactly what it sounds like it aims to prevent sickness before it happens.

The ideology behind preventive medicine focuses on protecting, promoting, and maintaining health and well-being. It also aims to avert disease, disability, and death on an individual basis, as well as on a large scale in communities and populations.

Preventive medicine is promoted by all physicians, though some choose to specialize in it. Physicians in this specialty use biostatistics and epidemiology, as well as a mix of medical, social, economic, and behavioral sciences. They may evaluate health services or manage health care organizations. They also study the cause of disease and injury within specific population segments.

Preventive medicine is an interdisciplinary branch of medicine that focuses on the whole patient and the many factors influencing their health. It holds a broad scope, encompassing elements of socioeconomics, the role of legislation, health equity, and the disparities found in communities and certain populations.

Chronic diseases, such as diabetes and heart disease, account for seven out of ten deaths, according to the Centers for Disease Control and Prevention (CDC). This is why screening and detection have become so critical. Healthy habits are just as critical, including eating well, exercising, and avoiding tobacco use. These help individuals stay healthy, avoid disease, or minimize the effects of disease.

The CDC lists the five leading causes of death in the US as heart disease, cancer, chronic lower respiratory disease, stroke, and unintentional injuries. This makes preventive medicine all the more important in avoiding premature death.

Practicing preventive medicine can also lower costs, as 75 percent of annual health spending goes toward chronic and largely preventable diseases in the US, according to the CDC. Preventive medicine also fights the productivity drain associated with chronic illness.

Preventive medicine can be practiced in both the clinic setting and outside of it. Clinical preventive medicine physicians see patients. They may provide counseling for unhealthy habits, run preventive health screenings and administer immunizations. They may work with patients who would benefit from lifestyle changes and often encounter common cases such as diabetes, smoking, or obesity.

Non-clinical preventive medicine physicians dont work closely with individual patients. This branch of medicine includes health policy, epidemiology, and an increased focus on the social and behavioral influences on a persons health. However, the work of many preventive medicine physicians spans both the clinical and non-clinical branches of the field.

Additionally, the field of preventive medicine also offers several focused subspecialties, including the following:

Aerospace medicine pertains to the health and safety of persons within air and space vehicles. The passengers and workers aboard these contraptions face their share of environmental hazards, as well as physical and psychological stressors.

Physicians in aerospace medicine work to promote the health, safety, and wellness of individuals working or travelling in air and space environments. They work to prevent injury from many environmental factors, including microgravity, radiation exposure, G-forces, emergency ejection injuries, and hypoxic conditions.

Occupational medicine seeks to prevent injury, disability, and death in workers. Physicians specializing in occupational medicine examine the physical, chemical, biological, and social environments of the workplace and their impact on the health of employees. They help employers identify health and safety risks to employees and work to cut down on occupational hazards that could result in injury or death. They may also make policy recommendations to promote safe work environments, diagnose occupational diseases and injuries, and research work-related health issues.

The public health medical specialty promotes health and well-being on a larger scale. These physicians work with communities and certain segments of the population, combining prevention-based clinical knowledge with population-based public health.

Public health physicians analyze data on public health problems and research the causes behind them. They also develop strategies to tackle health issues in the public, which can lead to new programs promoting overall health and preventing the spread of disease. Public health physicians also consult with other officials in the field to develop legislation benefitting the health of entire communities.

Now you know about what preventive medicine is and how doctors incorporate it into their practice or specialize in it altogether. This is an important field of medicine that not only helps patients and populations thwart illness, but also helps keeps health costs down.

As mentioned above, all doctors incorporate some degree of preventive medicine into their practice. But primary care physicians have an especially good opportunity to help their patients stay healthy and avoid falling ill. Learn more about the important role these doctors play in our article, What Does a Primary Care Physician Do? Exploring This High-Demand Medical Career.

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Stem Cell Therapy For Neuropathy | Stem Cell Therapy

September 15th, 2019 6:41 pm

Stem Cell Therapy for Neuropathy

Neuropathy is a condition characterized by pain of the limbs, such as arms, hands, feet, and/or legs. Neuropathic (nerve-related) pain is initiated/caused by dysfunction of the nervous system. Most common symptoms of neuropathy include extreme sensitivity and dramatic response to pain. A new, innovative treatment for neuropathy is stem cell therapy.

Neuropathy and nerve-related pain reduces human well-being and is difficult to manage. Around 100 million people in the United States report chronic pain. The use of stem cells has proven to be effective at lessening the pain associated with diabetic neuropathy and peripheral nerve pain. Clinical evidence shows that stem cell therapy provides the best results and could decrease the use of pain medication.

How do stem cells work to treat neuropathic pain?

Stem cell therapy shows great promise for regenerative medicine in the treatment of peripheral neuropathy. Stem cells help slow the disease progression. In rat subjects, bone marrow-derived stem cells have shown promise in treating neurodegenerative disease, which proves neuroprotective when given intravenously (IV). Stem cell implantation has also been shown to work in the repair of axon regeneration and synapse reformation, which are structures of the nerve cell.

Do stem cells help treat pain?

Stem cell differentiation is thought to be the key to pain control. Serotonergic neural precursor cell grafts reduce hyperexcitability caused by pain. Neuropathic pain causes a decrease in the activity and number of neurons called GABA. The stem cells express anti-nociceptive molecules and/or trophic factors that have been found to relieve neuropathic pain. In addition, stem cells are used as pumps to deliver anti-nociceptive molecules close to the pain processing sites of nerve damage.

Which cells are most used in the treatment of peripheral neuropathy?

Mesenchymal stem cells (MSCs) are showing the most promise in pain care research. These cells are a group of progenitor cells of mesodermal origin, which are found in adult bone marrow. These cells give rise to skeletal muscle cells, fat, blood, and connective tissues. MSCs also have a stable phenotype and are easily transported from the laboratory to physician office. These cells also migrate to the site of nerve damage and have good immunosuppressive properties.

Do clinical studies support the use of stem cells for peripheral neuropathy?

In a recent study in The Journal of Pain Research, researchers used stem cells for neuropathy relief successfully. They found that the treatment produced 60% relief at a six month time point. Because neuropathic pain impacts quality of life, it can be quite costly to the healthcare system. Researchers are continuing to study this problem.

Tulane University Center for Stem Cell Research conducted many studies using MSCs. They found these cells were effective and safe for treating inflammatory disease, such as peripheral neuropathy. The cells were found to optimize their anti-inflammatory effects. In mice subjects, researchers noted a 40% improvement rate.

What results can I expect with stem cell therapy for neuropathy?

Response to stem cell therapy usually starts within a few weeks to months. Patients often report effectiveness within 3-6 months. Patients with peripheral neuropathy respond over 60% of the time, according to studies. A second treatment may become necessary depending on the individual and therapy also involves several additional modalities such as light therapy and nutritional optimization.

Resources

Siniscalco D, Rossi F, & Maione S (2007). tem cell therapy for neuropathic pain treatment. J Stem Cells Regen Md, 3(1), 2-11.

A preliminary report on stem cell therapy for neuropathic pain in humans, Vickers et al,J Pain Res. 2014; 7: 255263.

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Stem Cell Therapy for Neuropathy | Mayo Clinic Connect

September 15th, 2019 6:41 pm

Hi @jlsoerensOne of the focus areas on Mayo Clinic's Regenerative Medicine Program is in neuroregeneration. You can read more here: https://www.mayo.edu/research/centers-programs/center-regenerative-medicine/focus-areas/neuroregeneration Scroll down the page and you can read clinical research being done specifically for peripheral nerve regeneration and repair.

Unfortunately, because of the complexity of the brain and spinal cord, little spontaneous regeneration, repair or healing occurs. Therefore, brain damage, paralysis from spinal cord injury and peripheral nerve damage are often permanent and incapacitating.

To learn more, you may wish to contact Mayo Clinics Regenerative Medicine free Consult Service. If you call them, you will talk to a live person who will provide more information, research, and advice on seeking stem cell therapy from reputable providers, even if that provider is not Mayo Clinic. Their primary goal is to educate and help you find effective treatment. Furthermore, you can add your name to a database to be notified when additional studies and information become available. Heres more information about the stem cell Consult Service http://www.mayo.edu/research/centers-programs/center-regenerative-medicine/patient-care/clinical-services/regenerative-medicine-consult-service. Or simply call 1-844-276-2003 to speak with one of our experts.

I also feel it important to add it is so important to do your homework and due diligence when researching new treatment options. Stem cells offer a lot of hope. But where these is hope, there is hype and charlatans. FDA acts to remove unproven, potentially harmful treatment used in stem cell centers targeting vulnerable patients https://www.fda.gov/newsevents/newsroom/pressannouncements/ucm573427.htm

You can read more about stem cells on the FDAs website here: https://www.fda.gov/AboutFDA/Transparency/Basics/ucm194655.htm

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Diabetes: Symptoms, Treatments, Causes, Tests & Preventions

September 15th, 2019 6:41 pm

Diabetes mellitus (DM) is the body's inability to regulate the level of glucose in the blood. Glucose is the main form of sugar in the body. The body breaks down food into glucose and uses it as a source of energy. In healthy people insulin helps to regulate the glucose (sugar) levels. Insulin is a hormone produced by the pancreas (a long, thin organ located behind the stomach against the back).

In diabetics, the body does not produce enough insulin or does not use the produced insulin effectively. This results in a high level of glucose in the blood ("hyperglycaemia").

There are three main types of diabetes mellitus:

a) Type 1, earlier known as insulin dependent diabetes mellitus (IDDM) or juvenile-onset diabetes mellitus. People with this type of diabetes make little or no insulin in their body, and need regular insulin injections for survival and management of diabetes. It usually starts in childhood, but can occur at any age. This ususally happen before age of 40.

b) Type 2 (DM2), earlier known as non-insulin dependent diabetes mellitus (NIDDM) or adult-onset diabetes. This is the most common form of diabetes, and is strongly associated with genetic tendency and obesity. The body produces normal or even high levels of insulin, but certain factors make its utilization ineffective ("insulin resistance"). Sedentary lifestyle, unhealthy dietary patterns, and the consequent obesity are common causes. It usually starts in adulthood, but is beginning to be seen in obese adolescents also.

c) Gestational diabetes mellitus, or pregnancy-induced diabetes.

Gestational diabetes is raised blood glucose levels during pregnancy. It develops in 5 % of all pregnancies but usually disappears when a pregnancy is over. Women who have had gestational diabetes are at increased risk (up to 40%) for later developing type 2 diabetes

Symptoms depend on the type and duration of diabetes. Some of the signs and symptoms are related to the high blood sugar levels.

These include: Increased urination, Increased thirst, Hunger

Other common symptoms:

There may be weight loss, especially if the amount of insulin made by the body is decreasing. If insulin deficiency is marked, the person can become drowsy and then go into coma. This is called Ketoacidosis, and usually occurs in DM1. Rarely, if the diabetes is completely out of control, it can also occur in DM2. Other symptoms of ketoacidosis include: Deep rapid breathing, sometimes with a fruity odour to the breath Pain in the stomach, with nausea and vomiting.

Diabetes mellitus is diagnosed based on a high level of glucose or sugar in the blood. The doctor may suspect diabetes mellitus after taking the medical history and doing a physical examination. There are several blood sugar tests used for diagnosis:

Fasting plasma glucose test: In this test, a person is asked to fast overnight, at least 8 hours, and the level of glucose in the blood is then checked. Normal fasting plasma glucose levels are less than 110 mg/dl. A fasting plasma glucose level of more than 126 mg/dl usually indicates diabetes mellitus. A level of 110-125 mg/dl is called "impaired fasting glucose".

Post prandial (PP) plasma glucose: This is tested two hours after having a meal, which serves as a challenge for the body to regulate the blood sugar. Normal PP levels are <140 mg/dl; a glucose level of more than 200 mg/dl indicates diabetes mellitus, while a level between 140-199 mg/ dl is called "impaired glucose tolerance".

Random plasma glucose test: is that which is done at any other time. A level of 200 mg/dl or higher generally indicates the presence of diabetes.

Oral glucose challenge test (oGTT): The blood glucose is tested 2 hours after giving 75 gm glucose by mouth. This is useful for detecting borderline diabetes and a condition called "impaired glucose tolerance".

Oral glucose tolerance test: is the preferred way to diagnose pregnancy-induced diabetes. Ideally all pregnant women in India should have a blood glucose test done 30 minutes after taking 50 gm gluocse (screening test). If this is abnormal, the lady should undergo an oGTT: with 100 gm glucose (not the conventional 75 gm). Blood samples are then drawn at intervals of one hour upto 3 hours (ie at 1, 2 and 3 hours post-glucose).

Although diabetes cannot be cured, it can be controlled very successfully. The main aim of treatment of all types of diabetes is to achieve blood glucose control, blood pressure and cholesterol levels as near to normal as possible. This, together with a healthy lifestyle, will help to improve wellbeing and protect against long-term complications.

Stay Active

Being active is good for all of us but is especially important for people with diabetes. Physical activity, combined with healthy eating and medication that you may taking will help you to manage your diabetes and prevent long term complications. If you have concerns at all about becoming active, never be afraid to ask for advice.

What are the Medication

People with diabetes often need additional treatment along with making lifestyle changes such as medication to control their Blood Pressure and blood fats. Treatment is decided by your specialist. But you should be aware of timings, dosage and its function in the body.

In diabetes stopping the treatment by your own can create lots of problems.

Hypoglycemia is the common problem which can happen in pt who is being treated with oral medications or Insulin

Hypoglycemia (low blood sugar) can be life threatening condition and its very important to act early.

Low blood sugar: a level below about 60 milligrams per deciliter (mg/dl) occurs when there's too much insulin and not enough sugar (glucose) in your blood. Low blood sugar is most common among people taking insulin, but it can also occur if you're taking oral diabetes medications.

When your blood sugar is low you may feel:

Shaky or nervous, Tired, Sweaty, Hungry, Irritable, Impatient, Cold, Confused

You may also feel tingling around your mouth.

Reasons for blood sugar swings

Although it is frustrating, blood sugar levels can also be too high for no clear reason.

Sometimes these high levels may be the first sign of an infection, illness or stress.

Because blood sugar levels can go very high when you are ill, talk with your health care team about creating a sick day plan to manage your diabetes when you have a cold, flu or other illness.

Pre Diabetes

Pre diabetes is when one has higher than normal glucose level but not high enough to be diagnosed with diabetes. Pre-diabetes is present when hba1c is over 6% -6.4%.

A person with pre-diabetes can be prevented to develop Diabetes by:

1. Improving diet

2. Increasing physical activity at least 30 minutes for 5 days in a week.

3. By reducing body weight, high blood glucose levels can return to normal which reduces the likelihood of developing T2D.

Benefits of weight loss

Benefits of an active lifestyle

Maintaining a healthy weight and eating a healthy balanced diet, low in fat and rich in fiber and fruits and vegetables, as well as being physically active is an important part of managing blood sugar levels and avoiding other health complications.

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16 Early Signs of Diabetes – diabetics.guide

September 15th, 2019 6:41 pm

March 19, 2018 | More Articles: Symptoms

Type 2 diabetes is one of the major degenerative diseases in the Western world today. It happens when your body cant use insulin properly, or cant make enough insulin. Insulin is a hormone the assists the bodys cells in utilizing glucose. It also helps the body store extra sugar in fat, liver, and muscle cells. If you dont have insulin, your body cant use the sugar in the bloodstream.

Then, your blood sugar levels get too high. High blood sugar can have a deleterious effect on many parts of your body, including heart, blood vessels, nerves, eyes, and kidneys. Those who are overweight, dont exercise enough, or have a history of type 2 diabetes in their family are more likely to get the disease. Maintaining a healthy weight, eating a healthy diet, and getting enough exercise can prevent type 2 diabetes. If you have a history of diabetes in your family, or if you are overweight, stay ahead of the disease by making healthy lifestyle choices and changing your diet.

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Frequent urination is an early warning symptom of diabetes. When there is too much glucose in the blood, the kidneys work overtime to flush it out of the blood via urination. So, youll find yourself going to bathroom a lot more often than normal. There is also a bigger risk of urinary tractions in both men and women.

Individuals with diabetes have two times the likelihood of getting a urinary tract infection compared to individuals without the disease. If you find yourself getting up every couple of hours in the middle of the night, and you seem to be expelling a lot more urine than you used to, talk to your doctor and find out whether or not you have diabetes.

Increased urinary frequency is called polyuria, and individuals with diabetes are unable to regulate blood sugar levels. When too much sugars in the bloodstream, more fluids will pass through your kidneys.

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What is diabetes? – Diabetes Canada

September 15th, 2019 6:41 pm

The importance of insulin

Diabetes is a disease in which your body either can't produce insulin or can't properly use the insulin it produces. Insulin is a hormone produced by your pancreas.

Insulin's role is to regulate the amount of glucose (sugar) in the blood. Blood sugar must be carefully regulated to ensure that the body functions properly. Too much blood sugar can cause damage to organs, blood vessels, and nerves. Your body also needs insulin in order to use sugar for energy.

Eleven million Canadians are living with diabetes or prediabetes. Chances are, diabetes affects you or someone you know.

There are three major types of diabetes. Type 2 diabetes is the most common diagnosis, followed by type 1 diabetes. Gestational diabetes occurs during pregnancy, and is usually temporary. In addition, prediabetes is another important diagnosis that indicates an elevated risk of developing diabetes.

Type 1 diabetes is an autoimmune disease and is also known as insulin-dependent diabetes. People with type 1 diabetes aren't able to produce their own insulin (and can't regulate their blood sugar) because their body is attacking the pancreas. Roughly 10 per cent of people living with diabetes have type 1, insulin-dependent diabetes.

Type 1 diabetes generally develops in childhood or adolescence, but can also develop in adulthood. People with type 1 need to inject insulin or use an insulin pump to ensure their bodies have the right amount of insulin.

People with type 2 diabetes can't properly use the insulin made by their bodies, or their bodies aren't able to produce enough insulin. Roughly 90 per cent of people living with diabetes have type 2 diabetes.

Type 2 diabetes is most commonly developed in adulthood, although it can also occur in childhood.Type 2 diabetes can sometimes be managed with healthy eating and regular exercise alone, but may also require medications or insulin therapy.

If you think you or someone you know may have type 2 diabetes, please speak to a doctor or health-care provider.

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What is diabetes? - Diabetes Canada

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Diabetes – research.va.gov

September 15th, 2019 6:41 pm

VA research on Diabetes Introduction

Diabetes is a chronic disease in which the body cannot produce or properly use insulin. Normally, insulin brings sugar out of the bloodstream and into cells. If the body cannot make insulin or does not respond to it, the sugar stays in the bloodstream. As a result of high blood sugar levels, damage eventually occurs to blood vessels and organs.

More than 29 million Americans have diabetes, according to the Centers for Disease Control and Prevention, and 86 million more Americans are at risk to develop the disease. Many Veterans have the disease, including some who developed it as a result of being exposed to herbicides while serving in Vietnam.

Symptoms of diabetes include blurry vision, excessive thirst, fatigue, frequent urination, hunger, and weight loss. Persons with diabetes need to have their hemoglobin A1C levels checked every three to six months.

A1c is a measure of average blood glucose during the previous two to three months. It is one of the markers, along with blood pressure and cholesterol control, of good diabetes care.

There are three major types of diabetes. Type 1 diabetes is usually diagnosed in childhood. In this type of diabetes the body makes little or no insulin, so daily injections of insulin are needed.

Type 2 diabetes usually occurs in adults. In this type of diabetes, the pancreas does not make enough insulin to keep blood glucose levels normal, often because the body does not respond well to insulin. More than 90 percent of adults with diabetes have type 2 diabetes. More are at risk due to overweight or obesity.

The third type of diabetes is gestational diabetes, high blood glucose that develops during pregnancy in a woman who does not have diabetes.

Diabetes affects nearly 25 percent of VA's patient population. The disease is also the leading cause of blindness, end-stage renal disease, and amputation for VA patients.

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VA researchers are studying innovative strategies and technologies, including group visits, telemedicine, peer counseling, and Internet-based education and case management, to enhance access to diabetes care and to improve outcomes for patients.

In addition, VA researchers are working to develop better ways to prevent or treat diabetes, especially in special populations such as the elderly, amputees, minorities, spinal cord injured patients, and those with kidney or heart disease.

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Two of VA's three Nobel laureates have done important work to benefit Veterans with diabetes. The late Dr. Rosalyn S. Yalow received the Nobel Prize for Physiology or Medicine in 1977 for her work in discovering the radioimmunoassay, an extremely sensitive way to measure insulin and other hormones in the blood. The technique made possible major advances in diabetes research and in diagnosing and treating hormonal problems related to growth, thyroid function, and fertility.

Dr. Andrew V. Schally also received the Nobel Prize in Physiology or Medicine in 1977 for his discovery that the hypothalamus links the nervous system to the endocrine system via the pituitary gland, is currently doing research, along with teams of national and international researchers, on growth hormone-releasing hormone (GHRH). Among other possibilities opened up by Schally's work with GHRH is the possibility of reducing or eliminating the need for diabetics to regularly inject insulin.

In 2013, an international research including Schally devised a way to transplant healthy cells into the body without the usual risk of rejection. The study involved a middle-aged man with diabetes, but it may be relevant to a range of other diseases as well. The researchers developed what amounts to an artificial pancreas (the place where the body makes insulin), which the patient tolerated well without taking drugs to suppress the immune system.

A 2015 study by Schally and his team evaluated newly developed GHRH agonists' ability to promote the growth and function of pancreatic islet cells, and found that these new agonists may provide an improved approach to treating diabetes. Agonists are substances that act like other substances and therefore stimulate an action in the body. Islet cells, also called Islets of Langerhans, sense blood sugar levels and release insulin to maintain normal levels.

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For seven and a half years, researchers involved in a VA cooperative study(CSP 465) looked at nearly 1,800 patients with diabetes. The researchers examined cardiovascular disease, the cause of death in nearly two-thirds of patients with diabetes.

Researchers attempted to determine whether intensive glucose control (using medication and other methods to reduce the level of sugar in the blood in diabetic patients to levels that would be normal in patients without diabetes) reduced heart attacks, strokes, and death from cardiovascular disease.

It had been previously shown that improvements in blood pressure and cholesterol levels can reduce cardiovascular disease in patients with diabetes, but no previous study had shown the beneficial effects of glucose control on cardiovascular disease.

VADT researchers showed that intensive glucose control in patients whose type 2 diabetes had previously been poorly controlled had no significant effect on the rates of major cardiovascular events such as coronary artery disease and stroke, compared to those who were using standard glucose control measures.

The research team also found that the two groups of patients had similar death rates, and that both groups had similar levels of complications such as diabetic neuropathy and retinopathy, except that patients using standard glucose control measures had higher levels of albumin in their urine. (Albumin in the urine is a possible indicator of kidney disease.)

Trial researchers concluded that both very high and very low blood sugar levels can be dangerous, and that big swings between high and low levels are also potentially harmful.

As a follow up to VADT, VA researchers looked at whether the improvements in glucose control made by one of the groups in the trial led to long-term improved consequences. They collected information on the VADT cohort for more than nine years of additional study, using VA's electronic records system.

The team found in 2015 that patients who had been in the intensive-control group had a lower incidence of cardiovascular events after the trial was over, but their survival rates were no better than those of the other group.

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Sleep apnea and poor sleep qualityA 2013 study conducted by researchers at the VA Puget Sound Health Care System that was part of the joint VA-Department of Defense Millennium Cohort Study on the health of service members and Veterans, found that sleep apnea and poor sleep quality predicted diabetes, independent of other diabetes risk factors or mental health status.

Sleep apnea increased the risk of diabetes by 78 percent, and simply having trouble sleeping increased the risk of diabetes by 21 percent. The study included more than 47,000 service members and Veterans who were an average age of about 49.

Statin useResearchers at the VA North Texas Health System and their colleagues examined the health records of tens of thousands of Tricare beneficiaries for a nearly 10-year period. Their study, published in 2015, found that the use of statins to lower cholesterol is associated with a significantly higher risk of new-onset diabeteseven in a very healthy population.

They also found that statin use is associated with a very high risk of diabetes complications in this healthy population, and with a higher risk of obesity. High-intensity statin therapy was associated with greater risks for all outcomes.

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Implantation of insulin-producing cellsInsulin-producing cells that respond to glucose and correct blood-sugar levels in diabetic mice have been created by researchers at the Iowa City VA Health Care System and correct blood-sugar levels in diabetic mice.

The researchers took human skin cells and reprogrammed them to create induced pluripotent stem (IPS) cells, which were then coaxed into forming insulin-producing cells. When these cells were transplanted into diabetic mice, the cells secreted insulin and reduced the blood sugar levels of the mice to normal or near normal-levels.

The study raises the possibility that patients with diabetes could be treated with their own cells, which will accelerate treatment.

GRADE trialVA researchers are participating in a five-year National Institutes of Health study to compare the long-term benefits and risks of four diabetes drugs in combination with metformin. The study, called the Glycemic Reduction Approaches in Diabetes (GRADE) trial, is expected to include some 5,000 participants nationwide.

Metformin is the first medication doctors typically use when treating type 2 diabetes. If metformin does not control the disease, doctors may add one of several other drugs, all of which have been shown to lower blood sugar levels in studies. However, no previous long-term study has focused on which drug combination works best and has the least side effects.

The four drugs being studied are sulfonylurea, dipeptidyl peptidase-4 inhibitor, glucagon-like peptide-1 agonist, and long-acting insulin.

Drug combination causes adverse effectsIn 2013, VA researchers stopped a large multicenter study, part of the Veterans Affairs Nephropathy in Diabetes Study (NEPHRON-D), before its scheduled conclusion. They found that the combination of an angiotensin-converting enzyme (ACE) inhibitor and an angiotensin-receptor blocker (ARB) increases the risk for serious adverse effects in patients with diabetic nephropathy, the leading cause of chronic kidney disease in the United States.

The significant increase in risk caused by taking the combination of drugs overshadowed any benefits taking the drugs may have in reducing the progression of kidney disease.

Diabetic kidney diseaseIn 2015, researchers participating in the NEPHRON-D study found that in patients with proteinuric diabetic kidney disease, a mean systolic blood pressure greater than 140 and a mean diastolic blood pressure greater than 80 were associated with a higher risk of kidney failure and death.

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The Veterans Affairs Implantable Insulin Pump Study; effect on cardiovascular risk factors. Duckworth WC, Saudek CD, Giobbie-Hurder A, Henderson WG, Henry RR, Kelley DE, Edelman SV, Zieve FJ, Adler RA, Anderson RJ, Hamilton BP, Donner TW, Kirkman MS, Morgan NA. Implantable insulin pump therapy in insulin-requiring patients with type 2 diabetes has advantages over multiple-dose insulin therapy in decreasing the requirement for antihypertensive therapy and for decreasing total and free insulin and insulin antibodies. Diabetes Care, 1998 Oct;21(10):1596-602.

Glucose control and vascular complications in veterans with type 2 diabetes. Duckworth W, Abraira C, Moritz T, Reda D, Emanuele N, Reaven PD, Zieve FJ, Marks J, Davis SN, Hayward R, Warren SR, Goldman S, McCarren M, Vitek ME, Henderson WG, Huang GD, VADT investigators. Intensive glucose control in patients with poorly controlled type 2 diabetes had no significant effect on the rates of major cardiovascular events, death, or microvascular complications with the exception of progression of albuminuria. N Engl J Med. 2009 Jan 8;360(2):129-39.

Agonist of growth hormone-releasing hormone as a potential effector for survival and proliferation of pancreatic islets . Ludwig B, Ziegler CG, Schally AV, Richter C, Steffen A, Jabs N, Funk RH, Brendel MD, Block NL, Ehrhart-Bornstein M, Bornstein SR. Evidence that agonists of GHRH represent a promising pharmacological therapy aimed at promoting islet graft growth and proliferation in diabetic patients. Proc Natl Acad Sci USA, 2010 Jul 13;107(28);12623-8.

Sleep characteristics, mental health, and diabetes risk: a prospective study of U.S. military service members in the Millennium Cohort Study. Boyko EJ, Seelig AD, Jacobson IG, Hooper TI, Smith B, Smith TC, Crum-Cianflone NF; Millennium Cohort Study Team. Trouble sleeping and sleep apnea predict diabetes risk independent of mental health conditions and other diabetes risk factors. Diabetes Care. 2013 Oct;36(10):3154-61.

Combined angiotensin inhibition for the treatment of diabetic nephropathy. Fried LF, Emanuele N, Zhang JH, Brophy M, Connor TA, Duckworth W, Leehey DJ, McCullogh PA, O'Connor T, Palevsky PM, Reilly RF, Seliger SL, Warren SR, Watnick S, Peduzzi P, Guarino P; VA NEPHRON-D investigators. Combination therapy with an angiotensin-converting-enzyme (ACE) inhibitor and an angiotensin-receptor-blocker (ARB) was associated with an increased risk of adverse events among patients with diabetic nephropathy. N Engl J Med. 2013 Nov 14;369(20); 1892-903.

Human iPS cell-derived insulin producing cells form vascularized organoids under the kidney capsules of diabetic mice. A pancreatic organ can be created in vivo, providing evidence that human iPS cells might be a novel option for the treatment of type 1 diabetes. PLoS One, 2015 Jan 28;10(1):e0116582.

Enriching the diet with menhaden oil improves peripheral neuropathy in streptozotocin-induced type 1 diabetic rats. Coppey LJ, Davidson EP, Obrosov A, Yorek MA. Enriching the diet with n-3 fatty acids may be a good treatment strategy for diabetic neuropathy. J Neurophysiol. 2015 Feb 1;113(3):701-8.

Follow-up of glycemic control and cardiovascular outcomes in type 2 diabetes. Hayward RA, Reaven PD, Wiitala WL, Bahn GD, Reda DJ, Ge L, McCarren M, Duckworth WC, Emanuele NV, VADT Investigators. After nearly 10 years of follow-up, patients with type 2 diabetes who had been randomly assigned to intensive glucose control for 5.6 years had 8.6 fewer major cardiovascular events per 1000 person years than those assigned to standard therapy, but no improvement was seen in the rate of overall survival. N Engl J Med. 2015 Jun 4; 372(23):2197-206.

Dipeptidyl peptidase-4 inhibition ameliorates Western diet-induced hepatic steatosis and insulin resistance through hepatic lipid remodeling and modulation of hepatic mitochondrial function.Aroor AR, Habibi J, Ford DA, Nistala R, Lastra G, Manrique C, Dunham MM, Ford KD, Thyfault JP, Parks EJ, Sowers JR, Rector RS. Mice fed a diet that includes a DPP-4 inhibitor were found to have less insulin resistance than those not given the inhibitor. Diabetes. 2015 Jun;64(6):1988-2001.

BP and Renal Outcomes in Diabetic Kidney Disease: The Veterans Affairs Nephropathy in Diabetes Trial. Leehey DJ, Zhang JH, Emanuele NV, Whaley-Connell A, Palevsky PM, Reilly RF, Guarino P, Fried LF; VA NEPHRON-D Study Group. In patients with proteinuric diabetic kidney disease, mean systolic blood pressure greater than or equal to 140 mmHg and mean diastolic blood pressure greater than or equal to 80 mmHg were associated with worse renal outcomes. Clin J Am Soc Nephrol. 2015 Oct 19. pii: CJN.02850315. [Epub ahead of print]

Beneficial effects of growth hormone-releasing hormone agonists on rat INS-1 cells and on streptozotocin-induced NOD/SCID mice. Zhang, X, Cui T,He J, Wang H, Cai R, Popovics P, Vidaurre I, Sha W, Schmid J, Ludwig B, Block NL, Bornstein SR, Schally AV. This study provides an improved approach to the therapeutic use of GHRH agonists in the treatment of diabetes mellitus. Proc Natl Acad SCi USA, 2015 Nov 3; 112(44):13651-6.

Practical telemedicine for Veterans with persistently poor diabetes control: a randomized pilot trial. Crowley MJ, Edelman D, McAndrew AT, Kistler S, Danus S, Webb JA, Zanga J, Sanders LL, Coffman CJ, Jackson Gl, Bosworth HB. A comprehensive telemedicine intervention improved outcomes among Veterans with persistently poor diabetes control despite clinic-based care. Telemed J E Health. 2015 Nov 5. (Epub ahead of print.)

Statins and New-- Mellitus and Diabetic Complications: A Retrospective Cohort Study of US Healthy Adults. Mansi I, Frei CR, Wang CP, Mortensen EM. Diabetes, diabetic complications, and overweight/obesity were more commonly diagnosed among statin users than similar nonusers in a healthy cohort of adults. J Gen Intern Med. 2015 Nov;30(11):1599-610.

Rates of deintensification of blood pressure and glycemic medication treatment based on levels of control and life expectancy in older patients with diabetes mellitus. Sussman JB, Kerr EA, Saini SD, Holleman RG, Klamerus ML, Min LC, Vijan S, Hofer TP. Physicians are not likely to cut back on blood pressure and glycemic medication treatments in older patients with diabetes after they reach low BP or hemoglobin A1c levels. JAMA Intern Med. 2015;175(12):1942-1949.

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Diabetes – A Major Risk Factor for Kidney Disease | National …

September 15th, 2019 6:41 pm

Diabetes mellitus, usually called diabetes, is a disease in which your body does not make enough insulin or cannot use normal amounts of insulin properly. Insulin is a hormone that regulates the amount of sugar in your blood. A high blood sugar level can cause problems in many parts of your body.

The most common ones are Type 1 and Type 2. Type 1 diabetes usually occurs in children. It is also called juvenile onset diabetes mellitus or insulin-dependent diabetes mellitus. In this type, your pancreas does not make enough insulin and you have to take insulin injections for the rest of your life.

Type 2 diabetes, which is more common, usually occurs in people over 40 and is called adult onset diabetes mellitus. It is also called non insulin-dependent diabetes mellitus. In Type 2, your pancreas makes insulin, but your body does not use it properly. The high blood sugar level often can be controlled by following a diet and/or taking medication, although some patients must take insulin. Type 2 diabetes is particularly prevalent among African Americans, American Indians, Latin Americans and Asian Americans.

With diabetes, the small blood vessels in the body are injured. When the blood vessels in the kidneys are injured, your kidneys cannot clean your blood properly. Your body will retain more water and salt than it should, which can result in weight gain and ankle swelling. You may have protein in your urine. Also, waste materials will build up in your blood.

Diabetes also may cause damage to nerves in your body. This can cause difficulty in emptying your bladder. The pressure resulting from your full bladder can back up and injure the kidneys. Also, if urine remains in your bladder for a long time, you can develop an infection from the rapid growth of bacteria in urine that has a high sugar level.

About 30 percent of patients with Type 1 (juvenile onset) diabetes and 10 to 40 percent of those with Type 2 (adult onset) diabetes eventually will suffer from kidney failure.

The earliest sign of diabetic kidney disease is an increased excretion of albumin in the urine. This is present long before the usual tests done in your doctor's office show evidence of kidney disease, so it is important for you to have this test on a yearly basis. Weight gain and ankle swelling may occur. You will use the bathroom more at night. Your blood pressure may get too high. As a person with diabetes, you should have your blood, urine and blood pressure checked at least once a year. This will lead to better control of your disease and early treatment of high blood pressure and kidney disease. Maintaining control of your diabetes can lower your risk of developing severe kidney disease.

As your kidneys fail, your blood urea nitrogen (BUN) levels will rise as well as the level of creatinine in your blood. You may also experience nausea, vomiting, a loss of appetite, weakness, increasing fatigue, itching, muscle cramps (especially in your legs) and anemia (a low blood count). You may find you need less insulin. This is because diseased kidneys cause less breakdown of insulin. If you develop any of these signs, call your doctor.

Signs of Kidney Disease in Patients with Diabetes

First, the doctor needs to find out if your diabetes has caused the injury. Other diseases can cause kidney damage. Your kidneys will work better and last longer if you:

If no other problems are found, your doctor will try to keep your kidneys working as long as possible. The use of high blood pressure medicines called angiotensin converting enzyme (ACE) inhibitors has been shown to help slow the loss of kidney function.

The kidney doctor, called a nephrologist, will plan your treatment with you, your family and your dietitian. Two things to keep in mind for keeping your kidneys healthy are controlling high blood pressure in conjunction with an ACE inhibitor and following your renal diabetic diet. Restricting protein in your diet also might be helpful. You and your dietitian can plan your diet together. For Kidney and Diabetes friendly recipes click here to visit our Kidney Kitchen.

End stage renal failure, or kidney failure, occurs when your kidneys are no longer able to support you in a reasonably healthy state, and dialysis or transplantation is needed. This happens when your kidneys function at only 10 to 15 percent.

Three types of treatment can be used once your kidneys have failed: kidney transplantation, hemodialysis and peritoneal dialysis. To learn more about treatment options for kidney failure click here.

Yes. Once you get a new kidney, you may need a higher dose of insulin. Your appetite will improve so your new kidney will break down insulin better than your injured one. You will use steroids to keep your body from rejecting your new kidney. If your new kidney fails, dialysis treatment can be started while you wait for another kidney. To learn more about kidney transplant click here.

Sometimes it is possible to perform a pancreas transplant along with a kidney transplant. Your doctor can advise you about this possibility.

Today, more and more research dollars are spent on diabetes research. Hopefully, the prevention and cure of diabetes is in our future. In the meantime, you can manage your diabetes better with:

If you would like more information, please contact us.

2015 National Kidney Foundation. All rights reserved. This material does not constitute medical advice. It is intended for informational purposes only. Please consult a physician for specific treatment recommendations.

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What Is Diabetes Mellitus? – articles.mercola.com

September 15th, 2019 6:40 pm

According to an analysis of global health trends from the year 1990 up to 2013,1 there has been a striking and alarming rise in the occurrence of diabetes mellitus, a trend that continues now, especially in the United States. In a study published in 2015, its said that at least 50 percent of American adults2 are now either in a state of prediabetes or are already struggling with the illness.

The American Diabetes Association says 30.3 million Americans, or 9.4 percent of the population, have diabetes, while 84.1 million U.S. adults age 18 and older had prediabetes.3 Even children are now being diagnosed with Type 2 diabetes, with the numbers continuing to rise.

Diabetes is an illness that can affect anyone. Its now a leading cause of death according to the Diabetes Research Institute, diabetes now takes more lives compared to breast cancer and AIDS combined claiming the life of one American every three minutes.4 But what exactly is diabetes mellitus? Why does it happen and how can you break free from it?

WebMD defines diabetes mellitus (also known simply as diabetes) as a chronic, lifelong condition that affects your body's ability to use the energy found in food.5 This is a group of metabolic diseases wherein the glucose that you get from food remains in your bloodstream (high blood sugar).

When you eat, your body transforms food into a special sugar (glucose) that your cells use for energy. However, in order for your cells to be able to take in the glucose and use it as fuel, it first needs a particular hormone called insulin.6 This essential hormone is produced in your pancreas.

In normal, healthy people, the pancreas does a good job of providing your body with just the right amount of insulin it needs. Insulin opens your cells and lets glucose enter so it can be used for energy.7

However, if you have diabetes, it means that your insulin production is inadequate, the body's cells do not respond properly to insulin, or a combination of these two factors. Because the cells are unable to take in the glucose, it then builds up in your blood where it wreaks havoc on your health.8

Aside from insulin, however, there are two more hormones that can predispose you to diabetes: leptin and ghrelin. Produced by your fat cells, leptin is a hormone that is responsible for telling the brain three things:

In addition, leptin is also necessary for your immune system, fertility and energy burning.

Meanwhile, ghrelin is the hormone that tells your body that youre hungry. Its secreted by the lining of your stomach. Since ghrelin is influenced by the growth hormone in your body, it tends to work differently in women and men.

These two hormones, along with insulin, are the three primary players (along with other factors) in the occurrence of diabetes.

If there is a problem in your bodys leptin or ghrelin signaling, then you tend to consume too much food for your activity level and metabolism rate, resulting in weight gain and obesity. And once obesity sets in, your cells become insulin-resistant, predisposing you to high blood glucose levels.

The excessively high levels of sugar in your blood cause damage to the tiny blood vessels in different body organs. This includes the heart, kidneys, nervous system and eyes. This is why diabetes has been widely associated with a wide range of health problems, including heart disease, kidney disease, eye problems and blindness, stroke and nerve damage in the feet.9

People with diabetes also experience various symptoms, the most common of which are frequent urination, increasing thirst and always being hungry.10

Living with diabetes can be emotionally and physically overwhelming. Its also a financial burden for most people annually, this illness costs the American public over $245 billion.11

The good news is that diabetes is potentially reversible and completely preventable without having to resort to conventional drugs. All it takes is a few disciplined lifestyle tweaks, particularly in your diet, so that you can avoid this damaging disease.

Diabetes: An Introduction

Causes of Diabetes

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Dental Stem Cells and Tooth Regeneration In 2019 celldent

September 14th, 2019 11:22 am

Teeth are the foremost natural, noninvasive source of stem cells. Dental stem cells, that are straightforward, convenient, and reasonable to gather, hold promise for a variety of very potential therapeutic applications. Dental stem cells provide an awfully promising therapeutic approach to restoring structural defects and this idea is extensively explored by many researchers that are obvious by the speedily growing literature in this field.

Dental problems caused by dental caries, periodontal disease and tooth injury compromise the oral and general health issues. Current advances in the development of regenerative therapy have been influenced by our understanding ofembryonic development, stem cell biology, and tissue engineering technology.Tooth regenerationis a field of regenerative medicine procedure within the field of tissue engineering and stem cell biology to exchange damaged or lost teeth by re-growing them from autologous stem cells.

Dental stem cells and cell-activating cytokines are thought to be candidate approach for tooth tissue regeneration as results of they have the potential to differentiate into tooth tissues in vitro and in vivo. Whole tooth replacement therapy is taken into consideration to be an attractive idea for next generation regenerative therapy as a type ofbioengineered organ replacement.Dental problems caused by dental caries, periodontal disease and tooth injury compromise the oral and general health issues. Current advances in the development of regenerative therapy have been influenced by our understanding of embryonic development, stem cell biology, and tissue engineering technology.Tooth regenerationis a field of regenerative medicine procedure within the field of tissue engineering and stem cell biology to exchange damaged or lost teeth by re-growing them from autologous stem cells.

Dental stem cells and cell-activating cytokines are thought to be candidate approach for tooth tissue regeneration as results of they have the potential to differentiate into tooth tissues in vitro and in vivo. Whole tooth replacement therapy is taken into consideration to be an attractive idea for next generation regenerative therapy as a type of bioengineered organ replacement.

Source:https://tissuesciencecongress.conferenceseries.com/

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Integrative Medicine and Health – Overview – Mayo Clinic

September 14th, 2019 11:22 am

When you're sick, medication or even surgery may be just what the doctor orders. Dr. Adam Perlman, an integrative health specialist at Mayo Clinic, asks an additional question.

"What else can we do to really improve our sense of well-being?"

That's where acupuncture, yoga or tai chi may be integrated into an overall plan of care. Dr. Perlman describes it as "really helping people to go beyond the treatment of disease and pathophysiology, to really a place where they are optimizing their vitality."

Evidence shows, for instance, that acupuncture can help with chronic pain and may be recommended to those with cancer, chronic fatigue and fibromyalgia.

Tai chi helps with balance and reduces falls in older adults. Yoga may help reduce stress, lower blood pressure and lower your heart rate.

But, Dr. Perlman says, it's not just what you do with your body that's important.

"Other things that tend to impact our health and well-being are things like gratitude and relationships."

For the Mayo Clinic News Network, I'm Vivien Williams.

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Gene therapy | medicine | Encyclopedia Britannica

September 14th, 2019 11:22 am

Gene therapy, also called gene transfer therapy, introduction of a normal gene into an individuals genome in order to repair a mutation that causes a genetic disease. When a normal gene is inserted into the nucleus of a mutant cell, the gene most likely will integrate into a chromosomal site different from the defective allele; although that may repair the mutation, a new mutation may result if the normal gene integrates into another functional gene. If the normal gene replaces the mutant allele, there is a chance that the transformed cells will proliferate and produce enough normal gene product for the entire body to be restored to the undiseased phenotype.

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cancer: Gene therapy

Knowledge about the genetic defects that lead to cancer suggests that cancer can be treated by fixing those altered genes. One strategy

Human gene therapy has been attempted on somatic (body) cells for diseases such as cystic fibrosis, adenosine deaminase deficiency, familial hypercholesterolemia, cancer, and severe combined immunodeficiency (SCID) syndrome. Somatic cells cured by gene therapy may reverse the symptoms of disease in the treated individual, but the modification is not passed on to the next generation. Germline gene therapy aims to place corrected cells inside the germ line (e.g., cells of the ovary or testis). If that is achieved, those cells will undergo meiosis and provide a normal gametic contribution to the next generation. Germline gene therapy has been achieved experimentally in animals but not in humans.

Scientists have also explored the possibility of combining gene therapy with stem cell therapy. In a preliminary test of that approach, scientists collected skin cells from a patient with alpha-1 antitrypsin deficiency (an inherited disorder associated with certain types of lung and liver disease), reprogrammed the cells into stem cells, corrected the causative gene mutation, and then stimulated the cells to mature into liver cells. The reprogrammed, genetically corrected cells functioned normally.

Prerequisites for gene therapy include finding the best delivery system (often a virus, typically referred to as a viral vector) for the gene, demonstrating that the transferred gene can express itself in the host cell, and establishing that the procedure is safe. Few clinical trials of gene therapy in humans have satisfied all those conditions, often because the delivery system fails to reach cells or the genes are not expressed by cells. Improved gene therapy systems are being developed by using nanotechnology. A promising application of that research involves packaging genes into nanoparticles that are targeted to cancer cells, thereby killing cancer cells specifically and leaving healthy cells unharmed.

Some aspects of gene therapy, including genetic manipulation and selection, research on embryonic tissue, and experimentation on human subjects, have aroused ethical controversy and safety concerns. Some objections to gene therapy are based on the view that humans should not play God and interfere in the natural order. On the other hand, others have argued that genetic engineering may be justified where it is consistent with the purposes of God as creator. Some critics are particularly concerned about the safety of germline gene therapy, because any harm caused by such treatment could be passed to successive generations. Benefits, however, would also be passed on indefinitely. There also has been concern that the use of somatic gene therapy may affect germ cells.

Although the successful use of somatic gene therapy has been reported, clinical trials have revealed risks. In 1999 American teenager Jesse Gelsinger died after having taken part in a gene therapy trial. In 2000 researchers in France announced that they had successfully used gene therapy to treat infants who suffered from X-linked SCID (XSCID; an inherited disorder that affects males). The researchers treated 11 patients, two of whom later developed a leukemia-like illness. Those outcomes highlight the difficulties foreseen in the use of viral vectors in somatic gene therapy. Although the viruses that are used as vectors are disabled so that they cannot replicate, patients may suffer an immune response.

Another concern associated with gene therapy is that it represents a form of eugenics, which aims to improve future generations through the selection of desired traits. Some have argued that gene therapy is eugenic but that it is a treatment that can be adopted to avoid disability. To others, such a view of gene therapy legitimates the so-called medical model of disability (in which disability is seen as an individual problem to be fixed with medicine) and raises peoples hopes for new treatments that may never materialize.

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Stem Cell Therapy for Autism at the Panama Stem Cell Institute

September 14th, 2019 11:22 am

May 2019

Parents Guide to Cord Blood Foundation interview with Dr. Neil Riordan

The founder of Parents Guide to Cord Blood Foundation, Dr. Verter, had the opportunity to interview Dr. Riordan, the founder of the Panama Stem Cell Institute, during the annual meeting of the Perinatal Stem Cell Society in March 2019. This coverage is important for parents because it provides a concise summary of the Panama protocol for autism treatment. For cord blood bankers, this illustrates some factors that can contribute to a successful stem cell clinic.

This interview does not constitute an endorsement of the Panama Stem Cell Institute.

Many parents today are seeking stem cell therapy for a child with autism at the Stem Cell Institute located in downtown Panama City. The Panama Stem Cell Institute was founded by Neil Riordan PA PhD. Dr. Riordan is also a founder of the Riordan Medical Institute in Texas, and is involved with several companies in the field of regenerative medicine.

The popularity of the Stem Cell Institute in Panama arises from several factors. The clinic provides therapies using specially screened and processed mesenchymal stem cells (MSC) sourced from umbilical cord (UC) tissue that has been donated after normal, healthy births. These UC-MSC can safely be given to patients without any matching to the donor. Since the Stem Cell Institute does not use cord blood, parents do not have to worry about whether they banked cord blood for their children, whether the cord blood they banked is viable, or how to ship the cord blood to Panama. Once accepted and scheduled for treatment, the family travels to Panama and the clinic provides the stem cells. Both the clinic and accompanying laboratory in Panama are fully licensed by the national medical authorities and adhere to international standards. Parents can feel confident that the therapy is legal, the stem cells are sourced and prepared in an affiliated laboratory, and the clinic is highly experienced. The waiting list at Panama is only a few months, which is important to parents who want to try stem cell therapy while their childs brain is still developing.

The Stem Cell Institute provides families with a comprehensive five-day package that includes expedited customs clearance and a hotel room at the Hilton, which is connected to the clinics office tower. The price ranges from around $13,000 to $18,000 depending on the childs weight. For children with autism, the first day of the treatment, a Monday, is dedicated to intake testing. On days Tuesday through Friday, the child receives daily intravenous infusions of stem cells suspended in sterile solution. The four infusions deliver a total dosage of 40 to 80 million UC-MSC, depending on the childs weight.

The safety profile of the Panama Stem Cell Institute is well established. Since the clinic opened in 2006, they have performed over 10,000 procedures, and currently they are treating up to 200 patients per month. A patient registry safety review performed over nine months in 2018 found 497 adverse events (AE) out of 3058 treatments administered, which is a rate of 16.2%. The vast majority of AE (15.8%) were mild symptoms, consisting of fatigue and headache. The worst AE, consisting of nausea and vomiting, were only reported by 0.13% of patients.

A clinical trial for autism, registered by the clinic in 2014, has been completed with 20 participants. A paper was submitted to a peer-reviewed medical journal and is currently under review. In the final paper, outcomes were measured using Autism Treatment Evaluation Checklist (ATEC) scores, Childhood Autism Rating Scale (CARS) scores, macrophage-derived chemokine (MDC) levels and activation-regulated chemokine (TARC) levels recorded at baseline and again at 13 weeks, 25 weeks, 37 weeks, 49 weeks, and 89 weeks post-therapy.

At the Perinatal Stem Cell Society meeting, Dr. Riordan presented data on 47 autism patients selected from the clinic patient registry (movie link at bottom of the page). Among these patients, 87% were boys, the median patient age was 7 years old, and the daily dose averaged 15.75 million UC-MSC. For these patients, ATEC scores were compared at baseline and six months. The scores showed improvements in the categories of speech, sociability, awareness, and behavior; and all of the improvements had high statistical significance.

Parents contemplating autism therapy at Panama are encouraged to rule out other conditions that can cause autism symptoms, such as genetic disorders and heavy metal poisoning. Normal blood test readings for heavy metals are mandatory before enrolling for therapy.

Parents wishing to learn more about autism therapy at the Stem Cell Institute in Panama can visit the autism treatment page on the clinic website. There is an unaffiliated Facebook group, Stem Cell Therapy for Autism, which is run by parents for parents as a forum to share experiences with stem cell therapy.

Parents Guide to Cord Blood Foundation explains the rationale behind autism therapy with either cord blood MNC or cord tissue MSC in our companion article, Everything parents should know about stem cell therapy for Autism.

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Cost of Stem Cell Transplant – Beike Biotechnology

September 14th, 2019 11:22 am

Stem cell treatment is regularly in the news around the world. Mostly the topics revolve around safety, efficacy, or ethics. health insurance, Lately however, the price of these treatments has also been highlighted. Our stem cell provider,Beike Biotechnology, recently released their new stem cell therapy protocol in hopes of cutting treatment cost.

Other treatment providers in the news have been advertising prices from 50,000 USD to 200,000 USD.

Despite the thousands of positive research papers and clinical trials showing the effectiveness of stem cells the treatment is not readily available in most countries, especially not at a reasonable price. In the USA for example, it is possible to receive a stem cell treatment for Multiple Sclerosis. The bad news is that it will cost around $125,000 per patient, not including any drugs or supportive therapies. Also, this type of cell therapy (hematopoietic stem cell transplant) is not effective in progressive MS.

Similarly, a New Zealand man with Multiple Sclerosis is traveling to Singapore for hematopoietic stem cell treatment. The cost of this treatment is $200,000. Also, according to Associate Professor Bronwen Connor from Auckland University, in regards to hematopoietic stem cell transplants international trials showed the symptoms could recur over time and there were also some deaths associated with the treatment that were higher than would be acceptable for clinical practice.

Our treatment, specifically the new protocol from Beike Biotechnology was designed with progressive conditions in mind and utilizes umbilical cord blood and mesenchymal adult stem cells, which have had no history of adverse side-effects in thousands of clinical trials and treatments.

Another news story highlighted a Spinal Cord Injury (SCI) patient who paid $50,000 for a treatment in Panama. At this time this patient has not seen any significant improvements.

Our medical team recommends extensive physical and occupational therapy in combination with stem cell treatment for Spinal Cord Injury SCI which is offered at our partner treatment center Better Being Hospital. Our stem cell treatment protocol includes 6 injections of umbilical cord mesenchymal stem cells over 25 days with intensive rehabilitation is almost half Panamasstem cell institute cost which is $31,000.

Also, late last year spinal epidural stimulation, in combination with stem cell therapy, was found to be a very effective treatment option for SCI, allowing patients to voluntarily move their previously paralyzed limbs. In total, our comprehensive stem cell + epidural stimulation treatment is less than $80,000 for a 45 day intensive rehabilitation.

Our comprehensive treatment using umbilical cord stem cellsstarts at $12,000. For detailed information regarding our treatment packages

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Boss Stem Cell – Official Dead Cells Wiki

September 14th, 2019 11:22 am

Boss Stem Cells (or simply Boss Cells) are permanent items that increase the difficulty of the game when active. The first one is acquired by beating the Hand of the King with no Boss Stem Cells active, the second by beating him with one active, and so on. However, the fifth Boss Stem Cell is obtained by beating the Giant with four active.

Boss Stem Cells can be injected and removed at the start of the game in the Tube. Each one makes the game significantly harder by increasing enemy tier, density, variety, and limiting healing options. On the other hand, higher difficulty levels also increase cells dropped from enemies and the level of the Legendary Forge, and allow access to new blueprints and bonus doors scattered through the levels. The doors show the number of Boss Stem Cells required to enter and shine blue if enough are currently active. The fifth Boss Cell is special in that it doesn't modify anything compared to the fourth until the Throne Room, where it grants access to a secret biome, the Astrolab, and the hidden final boss of the game in the Observatory.

- Reduce number of health fountains (only available every other level); transition areas without health fountains will instead give a mini recharge that will refill one use of health flask

+ Improves the level of the Legendary Forge by allowing you to increase the frequency of ++ items up to 100%

+ Unlocks a door in Prison Depths that goes to the Ancient Sewers

+ Allows you to collect the next Boss Stem Cell

- Removes all health fountains, but gain one mini recharge after each boss

+ Improves the level of the Legendary Forge by allowing you to increase the frequency of S items up to 25%

+ Multiplies the amount of dropped cells by 2 (effect also applies to cells found in containers)

+ Unlocks a door in Slumbering Sanctuary that goes to the Cavern

+ Unlocks a door in Forgotten Sepulcher that goes to Guardian's Haven

+ Allows you to collect the next Boss Stem Cell

- Removes all health fountains (individual flask recharges can only be bought in Food shops)

+ Improves the level of the Legendary Forge by allowing you to increase the frequency of S items up to 50%

+ Multiplies the amount of dropped cells by 2 (effect also applies to cells found in containers)

+ Improves Legendary items by having them grant +1 to all Stats

+ Unlocks a door in Ramparts that goes to the Insufferable Crypt

+ Allows you to collect the next Boss Stem Cell

- Removes all health fountains (individual flask recharges can only be bought in Food shops)

- Taking hits always causes Malaise

- Increases detection range of mobs and gives most of them the ability to teleport next to your position

- Some of the food found in levels is infected by the Malaise

+ Improves the level of the Legendary Forge by allowing you to increase the frequency of S items up to 100%

+ Improves Legendary items by having them grant +1 to all Stats

+ Multiplies the amount of dropped cells by 3 (effect also applies to cells found in containers)

- Removes all health fountains (individual flask recharges can only be bought in Food shops)

- Taking hits always causes Malaise

- Increases detection range of mobs and gives most of them the ability to teleport next to your position

- Some of the food found in levels is infected by the Malaise

- No Collector in transitions areas (collected blueprints are unlocked when you go past where Collector was standing)

+ Improves the level of the Legendary Forge by allowing you to increase the frequency of S items up to 100%

+ Improves Legendary items by having them grant +1 to all Stats

+ Multiplies the amount of dropped cells by 3 (effect also applies to cells found in containers)

+ Gives access to the Astrolab and the Observatory (Rise of the Giant DLC content)

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Boss Stem Cell - Official Dead Cells Wiki

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Genetic Engineering | Talking Glossary of Genetic Terms …

September 14th, 2019 11:21 am

Genetic engineering is a term that was first introduced into our language in the 1970s to describe the emerging field of recombinant DNA technology and some of the things that were going on. As most people who read textbooks and things know, recombinant DNA technology started with pretty simple things--cloning very small pieces of DNA and growing them in bacteria--and has evolved to an enormous field where whole genomes can be cloned and moved from cell to cell, to cell using variations of techniques that all would come under genetic engineering as a very broad definition. To me, genetic engineering, broadly defined, means that you are taking pieces of DNA and combining them with other pieces of DNA. [This] doesn't really happen in nature, but is something that you engineer in your own laboratory and test tubes. And then taking what you have engineered and propagating that in any number of different organisms that range from bacterial cells to yeast cells, to plants and animals. So while there isn't a precise definition of genetic engineering, I think it more defines an entire field of recombinant DNA technology, genomics, and genetics in the 2000s.

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Nanomedicine Conferences 2019 | Nanotechnology Meetings …

September 14th, 2019 11:20 am

Pharmaceutical Nanotechnology & Nanomedicine Congress 2019

LexisConferencesconsider it a privilege and a matter of great pride to host Conference on Pharmaceutical Nanotechnology & Nanomedicine Congressis to be held at Venice, Italyfor the duration of September13-14, 2019. On this auspicious occasion, Organizing Committee invites the participants from all over the world to take part in this annual flagship conference with the theme Exploring the Progress of Nanomedicinewith Trending Nanotechnologies. The conference will provide a forum for interaction among attendees on Pharmaceutical Nanotechnology, Development of Nanotechnology-enabled Devices, Micro Fluidics platform for Nano Particle Synthesis, Toxicology and Risk Assessment of Nanomedicine Systems, MedicalNano Devices and Biosensors, Synthesis of Nanoparticles for Drug Delivery, Nanomedicine for Immune System and Cancer Diagnosis & Therapy.

This global meeting will assemble the world leaders in the expanding fields related to Pharmaceutical Nanotechnology & Nanomedicine. It will create an interface among professionals, academic faculty members, Researchers, Nanotech representatives and students, Nanotechnologists, Manufacturing Medical Device and experts in the fields of Nanotechnology. industry practitioners.The Conference will also have a room for companies and/or institutions to present their services, products, revolutions and research results.

Global Market for Nanotechnology products was priced $22.9 billion in 2013 and unanticipated increased to about $26 billion in 2014. This market is await to reach about $64.2 billion by 2019; a compound annual growth rate (CAGR) is 19.8% from 2014 to 2019. The global market for nanotechnology-enabled printing technology was approximate to be at total $14 billion in 2013. The market is anticipate to grow at a compound annual growth rate (CAGR) of 17.7% over the next five years and to total $31.8 billion by 2018.

Details of Nanomedicine Congress 2019

Conference Name

Place

Date

Nanomedicine Congress 2019

Venice, Italy

September 13-14, 2019

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Legal Issues in Stem Cell Therapy in the U.S. – Royse Law Firm

September 14th, 2019 11:20 am

Jul 30, 2019|Fred Greguras

My wife has had osteoarthritis, sometimes called wear-and-tear arthritis, in both of her knees since 2011. She first saw an advertisement for stem cell treatment in 2012 and continued to do research on the treatment. Late in 2018, after ultrasounds on her knees and consultation with several doctors and clinics in California and Colorado, she decided to have stem cell therapy that could regenerate the meniscus cartilage of her knees. Such therapy is a minimally invasive procedure that has the potential to slow the progress of the arthritic damage, repair joint cartilage and avoid or delay invasive knee replacement surgery.Such therapy can help the body repair itself naturally.

We thought it was best to act now before her knees worsened since the earlier the stem cell treatment began, the greater the chances for a successful outcome there would be. The present lack of health insurance coverage was considered, but the treatment cost was reasonable given the potential to avoid more invasive surgery and the timing of treatment. Most insurance plans, including Medicare, define the procedure as experimental and investigational and do not cover the therapy.

Based on her research, my wife selected Dr. Jason Glowney of Boulder Biologics to perform the treatment. Her treatment took place in the second week of January, 2019, as an outpatient at a hospital in Boulder, Colorado. The procedure was completed in under four hours. She was injected with her own stem cells (called an autologous donation), reducing the risk of immune rejection and other complications.

The medical team used ultrasound to identify the best sites for injection into the damaged tissue of her knees. The same needle remained in each knee site during the treatment, but the injections in each step described below were all done with separate syringes in sequence. There was no mixture of any of the multiple components in a single syringe.

The doctor gave her light oral sedationto help her relax for the procedure and used local anesthetic at the points of cell harvest and injection. No general anesthetic was administered. The procedure began with a harvest of platelet-rich plasma (PRP) from her blood. Her blood was quickly processed through a centrifuge to separate the blood and concentrate the platelets in the plasma, which was then injected to fertilize the knee sites to enhance cell growth. The concentrated platelets contain growth factors along with bioactive proteins that help initiate and stimulate tissue repair and regeneration. (In late May, 2019, she had another PRP injection to stimulate and enhance the growth of the stem cells.)

The next step in the procedure was to harvest her bone marrow, centrifuge it into an injectable volume of aspirate concentrate and then inject the concentrate in both knees. The bone marrow aspirate contains stem cells that can help regenerate bone and cartilage.

The adipose (fat-derived) stem cells used in the next step compliment the bone marrow stem cells. The adipose cells were harvested by a minimally invasive liposuction procedure, centrifuged to isolate the cells and then injected in both knees. The fat on our bodies can be a rich source of stem cells.

Hundreds of thousands of cells were harvested and injected in each step in order to have an adequate number of stem cells for the treatment. The stem cells decide whether to differentiate into bone, meniscus or other cartilage or to simply renew.

My wife was given antibiotic (doxycycline) tablets to take at the end of the procedure and, for a period thereafter, to assist the differentiation process and to help decrease cartilage degradation.

As discussed in more detail below, the doctors procedure was designed to involve only simple human cellular and tissue products from the same patient and not to be a new biological product or drug which requires FDA approval. The procedure would be a new biological product or drug requiring FDA approval if there had been more than minimal manipulation of each component part. Even a mixture of a patients own stem cells and an antibiotic administered from the same syringe would be deemed a new biological product or drug by the FDA.

The doctor gave my wife guidelines for physical activity and medications during the post-injection period. The guidelines were designed to promote the growth of the stem cells to regenerate tissue. The cells are fragile, and she had to be careful not to cause too much stress or shearing on them which could impede growth. Her pain was intense during the first 24 hours, and she stayed in bed much of the time. She used a walker for about the first week. She started physical therapy about six days after the injections with the doctors approval. The doctor recommended that she not take any anti-inflammatory medications (like ibuprofen or motrin), for six weeks since they could impede the differentiation of the stem cells. The doctor advised her that most patients dont feel any knee improvement for at leastthree weeksand possibly for up to six to eight weeks. If there is no improvement by the six-month point after the injections, then the therapy has not worked.

A self-reporting instrument is used for assessing a patients knee status. The 33 items measured are intended to represent all major indicators of knee status. My wifes measures are all very positive at this six-month point after the procedure. The measurement factors include: (1) knee symptoms such as knee swelling, stiffness and frequency of pain; (2) amount of pain in activities such as walking, standing and going up and down stairs; and (3) degree of difficulty in activities such as walking, bending down and going up and down stairs. Each item is rated on a five-point scale relating to the extent of its occurrence or severity during the past week.

Stem cells are different from other cell types in our bodies because they are capable of renewing (copying) themselves through cell division, sometimes after long periods of inactivity. Stem cells also have the potential to differentiate into other cell types in our body. When a stem cell divides, each new cell has the potential either to remain a stem cell or to differentiate into more specialized cells that form the bodys tissues and organs. In some organs, stem cells regularly divide to repair and replace worn out or damaged tissues. In other organs, stem cells only divide under special conditions.

There are several types of stem cells that are formed at different times in our lives orcome from different places in our body. Embryonic stem cells(ESCs) exist in the embryo only at the earliest stages of human development. ESCs are pluripotent, meaning they have the potential to differentiate into almost all cell types in the body. There are social and ethical issues relating to the use of ESCs, since harvesting the cells causes the destruction of an embryo. Many countries, including the U.S., have government-imposed restrictions on either ESC research or the production of new ESC lines.

Somatic or adult non-embryonic tissue-specific stem cells (ASCs) exist in specific tissues throughout the body after early human development. The stem cells injected into my wifes knees were ASCs. ASCs are multipotent, meaning they can differentiate into more than one type of specialized cell of the body, but not all types. ASCs are generally limited to differentiating into cell types of their tissue of origin, which can help with the replacement of cells from damaged tissue. ASCs can be an autologous stem cell donation, which is less likely to be rejected.

Amniotic stem cells (AMSCs) exist in the amniotic sac, which surrounds a baby in the uterus and remains until the babys birth. AMSCs are harvested right after the mother gives birth, without harming the baby. Some clinics make exaggerated claims about the therapeutic potential of ASMCs. AMSCs, however, are also multipotent, and the tissues they can differentiate into are substantially the same as stem cells from adipose (fat) and bone marrow. AMSCs exist only for a limited time, but adipose and bone marrow ASCs continue to be produced throughout our lives and can be harvested from the patient seeking therapy.

Some tissues and organs contain small amounts of ASCs whose function is to replace cells from that same tissue that deteriorate over time or are damaged by injury. For example, blood-forming stem cells in bone marrow can differentiate into red blood cells, white blood cells and platelets. However, blood-forming stem cells dont generate liver or lung or brain cells, and stem cells in other tissues and organs dont generate red or white blood cells or platelets.

Pluripotent stem cells have great therapeutic potential but still have major technical issues. Scientists cant control their differentiation into the many types of cells in the body which can result in unwanted tissue such as tumors. Since such stem cells are not from the recipient, they may also lack the compatibility needed to prevent rejection by the immune system.

Over 10 years ago, researchers identified conditions that enabled some specialized ASCs to be reprogrammed genetically back to an ESC-like state. The reprogrammed cells function similarly to ESCs and are called induced pluripotent stem cells (iPSCs). The iPSCs function similarly to ESCs, with the ability to differentiate into almost any cell of the body and to create an unlimited source of cells. iPSCs may ultimately help address the ethical concerns of ESCs and provide new potential for therapy, but there are still technical issues including whether they are actually equivalent to ESCs and the capability to control the differentiation process.

While the U.S. Food and Drug Administration (FDA) moves agonizingly slowly, its priority is human safety which is not the case in many other countries. Some other countries are the Wild West of stem cell therapy and have become medical tourism destinations for high-risk stem cell treatment. The FDA recommends that stem cell therapy is either FDA-approved or is done pursuant to an Investigational New Drug Application (IND), a clinical investigation plan submitted to and permitted to proceed by the FDA.There are many active clinical trials investigating the potential of ASCs listed on the U.S. National Institutes of Healths website.[1] Stem cell products approved by the FDA are listed on its web site.[2] There is no FDA-approved therapy involving the transplantation of ESCs. ESCs must be not be added to an injection, such as PRP, before it goes into a human.

The FDA regulates human tissues intended for transplant under 21 C.F.R. Part 1271: Human Cells, Tissues and Cellular and Tissue-Based Products (HCT/Ps). Cellular and tissue-based therapies are regulated by the Office of Cellular, Tissue and Gene Therapies within the FDA Center for Biologics Evaluation. There are two primary regulatory pathways for these products. Cellular therapy products that meet all the criteria in 21 CFR 1271.10(a) are regulated solely as HCT/Ps and are not required to be licensed, approved or cleared by the FDA. These products are often referred to as 361 products because they are regulated solely under Section 361 of the Public Health Service Act (PHSA).[3]The regulatory purpose for such products is to prevent the introduction, transmission and spread of communicable diseases.

If a cellular therapy product does not meet all the criteria in 21 CFR 1271.10(a), it is regulated as a drug, device and/or biological product under the Federal Food, Drug and Cosmetic Act (FDCA)[4] and Section 351 of the PHSA (a 351 product). The FDA requires premarket approval for such a product. The criteria that determine whether a product is a Section 361 HCT/P or a Section 351 biological product include, primarily, whether a product has been minimally manipulated and is intended for homologous use. Stem cell therapies generally do not satisfy these criteria and therefore are usually regulated as Section 351 products.

In the 2014 decision, United States of America v. Regenerative Sciences, LLC,[5] the court held that a mixture of autologous ASCs and other components was a 351 product and subject to FDA approval. Regenerative Sciences, LLC argued that its process did not create a mixture but only expanded the patients own cells and, therefore, was a simple 361 product which does not require FDA approval. The FDAs position is that any process involving human cellular and tissue products that includes culturing, expansion and added growth components or antibiotics requires FDA approval as a biological product or new drug because the process constitutes significant manipulation.

The FDA alleged that the product was a 351 product for failure to comply with its minimal manipulation provisions and because the resulting stem cells were not intended for homologous use. Homologous use means that a human cellular or tissue product is used clinically in a manner that is essentially the same as the natural function. The homologous use definition is strictly interpreted by the FDA, so that most innovative ways to use stem cells to potentially treat patients would be through non-homologous usage. The FDA will generally define even modestly different uses as non-homologous.

There are many clinics offering stem cell therapy in the U.S., some which carefully follow the law and others which do not. The FDA has only has brought a small number of enforcement actions because of resource limitations and proof concerns. Enforcement usually occurs in high-profile situations where a patient has died or is severely harmed.

The two important types of intellectual property protection relating to stem cell therapy are trade secret and patent protection. For example, the cell harvesting techniques and settings for the centrifuge processing in each step in my wifes treatment can be protected as trade secret know-how. The culturing and cocktails of growth factors and/or other components in the Regenerative Sciences, LLC case are another example.

There are many patents registered with the USPTO that contain the term stem cell, but recently, many human stem-based inventions have been rejected for not being eligible patentable subject matter. Patent-eligible subject matter is defined in 35 U.S.C. Section 101 as: Whoever invents or discovers any new and useful process, machine, manufacture or composition of matter, or any new and useful improvement thereof, may obtain a patent therefor, subject to the conditions and requirements of this title. There are three exceptions to subject matter eligibility: laws of nature, physical phenomena and abstract ideas.[6] The laws of nature exception has been the basis for rejection of patent eligibility for certain stem cell-related inventions.

There were two important court decisions in 1977 and 1980 relating to patent protection eligibility for the biotechnology industry.[7] The USPTO issued many stem cell patents following these decisions.

Several Supreme Court decisions in the past 10 years, however, have narrowed the scope of patent-eligible subject matter under Section 101.[8] In the Mayo decision, the Court held the invention was not patentable, stating that it effectively claimed the underlying laws of nature. The Court held that a claim that encompasses the use of a natural law must also include additional elements, sometimes referred to as an inventive concept, sufficient to ensure that the patent amounts to significantly morethan a patent upon the natural law itself.

The scope of patent-eligible subject matter was further narrowed in the Myriaddecision, which held that a naturally occurring DNA segment is a product of nature and not eligible for patent protection merely because it had been isolated. The Court looked for markedly different characteristics from any found in nature of the isolated gene to determine patent eligibility. The changes resulting from isolation of a gene sequence were considered incidental and not enough to make the isolated gene markedly different.

Three recent decisions in the Federal Circuit indicate that method-of-treatment claims that may involve a law of nature are patent-eligible.[9] Each of the patents required an affirmative treatment step. The decisions seem to hold that a patent directed to detecting a condition in a patient is not Section 101-eligible under Mayo, while a patent directed to using that detection to change some aspect of the patient is eligible. The patent may have been based upon the inventors discovery of a law of nature but the patent did not simply claim that law of nature. Rather, it was directed to a specific method of treatment.

The United States Patent and Trademark Office (USPTO) has published guidelines for patent examiners on how to analyze a claim which includes a nature-based product for patent eligibility.[10] Claims are to be examined for an inventiveness that has markedly different characteristics from naturally occurring products. Patent eligibility for a natural product is to be determined primarily by whether the claimed product possesses any structural, functional and/or other properties that represent markedly different characteristics from the natural counterpart. If the claim includes a nature-based product that has markedly different characteristics, then the claim is not within the product of nature exception. On the other hand, if the claim includes a nature-based product that does not have markedly different characteristics from its naturally occurring counterpart in its natural state, then the claim is within the product of nature exception and is not eligible for patent protection.[11]

The first step in the analysis is to select the counterpart(s) to compare to the nature-based product. The second step is to identify characteristics to compare, since the analysis is based on comparing the characteristics of the claimed nature-based product and its counterpart. Characteristics can be expressed as the nature-based products structure, function and/or other properties, and are evaluated on a case-by-case basis. The final step is to compare the characteristics of the claimed nature-based product to the characteristics of its naturally occurring counterpart in its natural state to determine if the characteristics of the claimed product are markedly different. If there is a change in at least one characteristic resulting from, or produced by, the patent applicants efforts or influences, then the change will generally be found to be a markedly different characteristic.

My wife was provided with disclosures from the doctors office and requested to sign a number of consents and waivers as a condition of receiving therapy. One of the waivers was a no assurance of successful treatment agreement.

State laws protecting consumers against deceptive advertising are applicable to representations about the effectiveness of stem cell treatment. Several state legislatures have debated additional protections for consumers relating to such treatment. California enacted a consumer protection law in late 2017 that requires clinics offering stem cell treatments to disclose if the treatment is not approved by the FDA.

The Federal Trade Commission (FTC) and FDA are pursuing enforcement actions in selected cases that may cause stem cell clinics to be more careful about their representations and activity. In late 2018, the FTC settled charges with a California-based physician and his businesses of deceptively advertising that amniotic stem cell therapy can treat serious diseases.[12] The settlement prohibits the defendants from making any health claims in the future unless the claims are true and supported by competent and reliable scientific evidence. This was the first enforcement action brought by the FTC against a stem cell clinic.

In early June, 2019, a federal judge granted the FDA an injunction to prevent the U.S. Stem Cell Clinic (based in Florida) from offering treatments using adipose stem cells injected into the spinal cords of patients to treat Parkinsons disease, chronic obstructive pulmonary disease and other serious conditions.[13] The court held that the defendants misbranded the possible therapeutic effects. The court also determined the clinic failed to prevent microbiological contamination of products which put patients at risk for infections.

As indicated, the status measures for my wifes knees are all very positive six months after the procedure. She is glad she tried it. I would try the therapy if I have problems with my knees.

The FDA will continue to move slowly to approve stem cell therapies since its priority is human safety. Some other countries have become medical tourism destinations for high-risk stem cell treatment. Many of the claims of such foreign clinics and of some clinics in the U.S. are medically unproven. The FDA and other regulators will continue to bring enforcement actions based on the severity of patient risk and available resources. Obtaining patent protection for stem cell-related inventions is challenging because of the subject matter eligibility issue under Section 101. The recent method-of-treatment decisions in the Federal Circuit may provide a helpful eligibility precedent for some inventions.

[1] See the NIHs website.

[2] See the Approved Cellular and Gene Therapy Products page on the FDAs website.

[3]42 U.S.C.(The Public Health and Welfare), Chapter 6A (Public Health Service).

[4] 21 U.S.C.

[5] 741 F.3d 1314 (D.C. Cir. 2014)

[6] Diamond v. Diehr, 450 U.S. 175 (1981).

[7] Diamond v. Chakrabarty, 447 U.S. 303 (1980); In re Bergy, 563 F.2d 1031 (1977)

[8] Mayo Collaborative Services v. Prometheus Laboratories, Inc., 566 U.S. 66 (2012); Association for Molecular Pathology v. Myriad Genetics, Inc., 569 U.S.576 (2013).

[9] SeeVanda Pharmaceuticals Inc. v. West-Ward Pharmaceuticals International Ltd.,887 F.3d 1117 (Fed. Cir. 2018) andNatural Alternatives International v. Creative Compounds, LLC, 2019 WL 1216226 (Fed. Cir. Mar. 15, 2019);Endo Pharmaceuticals Inc. v. Teva Pharmaceuticals USA, Inc. (Fed. Cir. 2019)

[10] See the 2106 Patent Subject Matter Eligibility [R-08.2017] page on the USPTOs website. The USPTOs Revised Patent Subject Matter Eligibility Guidance published in January, 2019, does not appear to add any guidance on claims including a natural product.

[11] A process claim is generally not subject to the markedly different analysis for nature-based products used in the process. The analysis of a process claim is supposed to focus on the active steps of the process rather than the products used in those steps.

[12] See the Federal Trade Commissions press release FTC Stops Deceptive Health Claims by a Stem Cell Therapy Clinic.

[13] See the U.S. Department of Justices news release Florida Company Barred from Using Experimental Stem Cell Drugs on Patients.

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Legal Issues in Stem Cell Therapy in the U.S. - Royse Law Firm

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Regenerating Body Parts: Fat Cells to Stem Cells to Repair …

September 14th, 2019 11:19 am

We often hear about the next big thing in stem cell therapy, though few of these promises eventuate or are backed up by evidence.

Well, we think were close to a genuine breakthrough in stem cell therapy, based on new research in Proceedings of the National Academy of Sciences.

We have developed a stem cell technique capable of regenerating any human tissue damaged by injury, disease or aging.The new technique, which reprograms bone and fat cells into induced multipotent stem cells (iMS), has successfully repaired bones and muscles in mice. Human trials are set to begin next year.

Injecting stem cells to repair damaged tissue is not a new concept. Every time someone receives a bone marrow transplant, they have in fact received blood stem cells to rescue their blood production.

But bone marrow is easy to extract and blood is constantly replaced. Therefore, blood stem cells are relatively easy to source.

This is not the case if you need stem cells to repair damage to muscles, cartilage or organs such as the heart and brain. These stem cells are not easy to extract and their turnover is low.

If stem cells are hard to extract, another option is to reprogram mature cells from other parts of the body that are relatively easy to extract. We have developed a method that converts fat or bone cells, which are relatively easy to extract, into induced multipotent stem cells.

This method involves culturing fat or bone cells with a drug called Azacitidine and a naturally occurring growth factor called platelet-derived growth factor. Azacitidine is used to treat blood disorders and has the ability to relax the hard-wired gene expression patterns that make a fat cell a fat cell or a bone cell a bone cell. We think the combination of erasing the cells memory with Azacitidine and forcing the cell to proliferate with the growth factor are key to converting fat and bone cells into induced multipotent stem cells.

UNSW.

The new technique is similar to the limb regeneration of the salamander, which can repair multiple tissue types, depending on which body part needs replacing.

In 2006, Japanese Nobel Prize-winning stem cell researcher Shinya Yamanaka identified a small number of genes that could reprogram skin cells from mice into immature stem cells, which could grow into all types of cells in the body.

However, these induced pluripotent stem (iPS) cells, like embryonic stem cells, which are derived from early embryos, are not suitable as a stem cell therapy because they can form tumours rather than repairing damaged tissue.

Since then, scientists have identified different combinations of genes that can reprogram skin or other cells into tissue-specific stem cells that only make cells of a single type of tissue.

A drawback with these reprogramming methods is the use of viral elements to force gene expression. Researchers use a virus as a mechanism to inject the gene into the cell.

Multipotent stem cells, in contrast, are produced without using any viral elements. They can regenerate damaged tissues without making unwanted tissues or tumors at the site of transplantation.

We have reprogrammed mouse bone cells into induced multipotent stem cells and injected these cells into mice with damaged bone and muscle.

We were astounded by the ability of these induced multipotent stem cells to regenerate these damaged tissues and also generate their own blood supply to carry nutrients to these developing tissues.

The transplanted cells appear to follow instructions from adjacent cells and divide and mature in an orderly fashion.

We are still investigating the safety and regenerative potential of human-induced multipotent stem cells.

We have injected human-induced multipotent stem cells, made by reprogramming human fat cells, into our animal models of tissue injury. We are monitoring signals from these cells and know they are retained at the site of injection.

In a few months, we will retrieve tissues from these mice to measure the contribution from transplanted human-induced multipotent stem cells to tissue regeneration in mice.

We need evidence of robust tissue regeneration and the absence of any unwanted tissues or tumours at these sites before commencing human trials.

The process of human induced multipotent stem cell production is free of animal products and is being developed to meet manufacturing standards appropriate for human cell transplantation.

Our initial clinical focus will be using induced multipotent stem cells either as a stand-alone treatment or with spinal implants to treat degenerative disc disease towards the end of 2017.

Low back and neck pain is frequently associated with degenerative disc disease and is a major cause of disability, affecting millions of people globally with crippling physical and economic costs.

Our aim is to use induced multipotent stem cells to regenerate discs to retain the flexibility of the native spine or to stabilise spinal implants by helping them fuse with adjacent bone.

We need further research to understand how mouse- and human-induced multipotent stem cells respond to signals from damaged tissues. It will also be important know how long induced multipotent stem cells remain at sites of transplantation and retain their ability to proliferate and make new tissues.

Nevertheless, this efficient virus-free method of generating tissue regenerative stem cells brings us a step closer to realising stem cell therapy for repairing tissue injury in the human body.

By John Pimanda, Associate Professor of Medicine and Stem Cell Biology, UNSW Australia; Ralph Mobbs, Neurosurgeon at the Prince of Wales Hospital; Conjoint Lecturer, UNSW Australia, and Vashe Chandrakanthan, Researcher, regenerative medicine, UNSW Australia. This article was originally published on The Conversation. Read the original article.

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