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Intermittent fasting over two days can help people with Type 2 diabetes – The Washington Post

Posted: June 24, 2024 at 2:40 am

Intermittent fasting can help people with Type 2 diabetes lose weight, lower blood pressure and improve blood sugar levels, a rigorous new study has found.

The new research, published Friday in the journal JAMA Network Open, found that intermittent fasting had striking metabolic benefits that surpassed even the effects of prescription medications for people with newly diagnosed diabetes. Here are the findings:

Courtney Peterson, an expert who was not involved in the study, said the results were exciting.

Often times we assume that drugs are more powerful than lifestyle approaches, said Peterson, an associate professor of nutrition sciences at the University of Alabama at Birmingham. But here they showed that a lifestyle approach was more effective for lowering blood sugar than putting people on drugs. Thats a very powerful statement.

The 5:2 diet was first popularized a decade ago by a BBC documentary and a best-selling book, The Fast Diet: Lose Weight, Stay Healthy, and Live Longer with the Simple Secret of Intermittent Fasting, by British physician Michael Mosley, along with co-writer Mimi Spencer.

The new study of the 5:2 diet took place in China, which has more people with Type 2 diabetes than any other country in the world. At least 141 million adults in China have diabetes and half the population is overweight or obese.

The authors of the new study recruited adults with Type 2 diabetes and then split them into three groups. In the first two groups, participants were assigned to take either metformin or empagliflozin. In the third group, participants were taught to follow the 5:2 diet. Women consumed just 500 calories on each of their two weekly fasting days, while men consumed no more than 600 calories equivalent to about a quarter of their usual caloric intake.

On their fasting days, the participants consumed sparse amounts of food: An egg for breakfast, a couple servings of fruit or vegetables for lunch, and a light salad for dinner. Each meal was paired with a low-calorie meal-replacement drink that contained healthy fats, protein, vitamins, minerals and other nutrients. On their non-fasting days, the participants would eat normally for breakfast and lunch and then have a light dinner with a meal-replacement drink.

In addition to losing weight, the fasting group saw their HbA1c, a long-term measure of their blood sugar levels, drop 1.9 percent significantly more than the groups taking medication. About 80 percent of participants in the fasting group saw their HbA1c fall below 6.5 percent, the cutoff for diabetes, compared to 60 percent of the participants on metformin and 55 percent of the people taking empagliflozin.

Eight weeks after the study ended, the researchers followed up with the participants and found that most of the people in the fasting group had maintained blood sugar levels below the threshold for diabetes, suggesting that the diet significantly and sustainably improves HbA1c levels, the authors wrote.

The researchers found that the fasting group also had greater reductions in their waist circumference, blood pressure levels and triglycerides, a type of fat that circulates in the blood, compared with the participants taking medication.

The researchers cautioned that more studies were needed to examine the long-term effectiveness of the 5:2 diet with meal replacements for Type 2 diabetes. But they said their findings suggest that the diet might be a good initial lifestyle intervention for people with early-stage diabetes.

Peterson said the study was large, rigorous and cleverly designed because it essentially combined two dietary interventions intermittent fasting and meal replacements that have been shown to help people with diabetes.

Many studies have found that diets that incorporate low-calorie meal-replacement shakes, soups and bars help people lose weight and lower their blood sugar levels. A number of studies have also indicated that the 5:2 diet helps people improve their blood sugar control.

Peterson said that one downside of the 5:2 diet is that people often see impressive results in the first few months, but that after about six months to a year on the diet, they start falling off.

It does seem to have an advantage in the short term, but in the long term which is a year or more, it doesnt seem to be better than a standard low-calorie diet, she added.

She also stressed that more long-term research was needed. But in the meantime, she said that people with newly diagnosed Type 2 diabetes might consider discussing with their doctor whether it is worth trying the 5:2 diet in combination with meal replacement shakes like Optifast, Ensure, Soylent or others.

She noted that while participants in the study did not experience many adverse events on the fasting regimen, about 6 percent of people on the diet reported symptoms of low-blood sugar, which can potentially be dangerous.

People should absolutely work with their doctor if they want to try this, Peterson said. They shouldnt try it on their own.

Do you have a question about healthy eating? Email EatingLab@washpost.com and we may answer your question in a future column.

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Diabetes Dialogue: ADA Introduces Obesity Association, with Robert Gabbay, MD, PhD – MD Magazine

Posted: June 24, 2024 at 2:39 am

On the opening day of the 84th American Diabetes Association Scientific Sessions, the ADA ushered in a new era for their organization with the announcement of the formation of the Obesity Association.

Created more than a decade after the American Medical Association recognized obesity as a disease, the new subdivision of the ADA was created to further the organizations mission of advocating for and advancing treatment for patients. According to a news release, the ADA intends to develop a Standards of Care for Obesity and to leverage education, advocacy and evidence-based support to reduce barriers to optimal care for people affected by diabetes for people with and without diabetes.

Clinical research is opening exciting new frontiers in the understanding and treatment of obesity. The ADA, through the Obesity Association, is uniquely positioned to translate these advances into weight wellness. We are eager to chart a new path in obesity care, said Robert Gabbay, MD, PhD, the chief scientific and medical officer of the ADA.

As part of the on-site coverage of ADA 2024, Diana Isaacs, PharmD, an endocrine clinical pharmacist, director of Education and Training in Diabetes Technology, and codirector of Endocrine Disorders in Pregnancy at the Cleveland Clinic, and Natalie Bellini, DNP, program director of Diabetes Technology at University Hospitals Diabetes and Metabolic Care Center, hosts of Diabetes Dialogue: Technology, Therapeutics, & Real-World Perspectives, sat down with Gabbay for more insight into the newly formed Obesity Association, future plans, and how this move reflects the changing landscape of metabolic health.

Relevant disclosures for Dr. Gabbay include American Diabetes Association and Harvard Medical School. Relevant disclosures for Dr. Bellini include Abbott Diabetes Care, MannKind, Provention Bio, and others. Relevant disclosures for Dr. Pantalone include Novo Nordisk, AstraZeneca, Bayer Inc., Corcept Therapeutics, Diasome, Eli Lilly and Company, Sanofi, and others. Dr Rodriguez has no disclosures.

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Mitochondrial metabolic reprogramming in diabetic kidney disease | Cell Death & Disease – Nature.com

Posted: June 24, 2024 at 2:39 am

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The American Diabetes Association Highlights Innovations in New Drug Therapies for Patients with Obesity – PR Newswire

Posted: June 24, 2024 at 2:39 am

Novel Drugs Demonstrate Benefits of Once Weekly Drugs for Weight Loss andGlycemic and Blood Pressure Control

ORLANDO, Fla., June 23, 2024 /PRNewswire/ -- Findings from three studies showcase new data on the latest developments in drug therapy innovations to treat obesity including new insights on GLP-1 (Glucagon-like peptide-1) receptor agonists. The data was presented as a late-breaking poster and oral presentations, respectively at the American Diabetes Association (ADA) 84th Scientific Sessions in Orlando, FL.

The studies are part of a host of research and development driven by interest in new GLP-1 drugs and concerns about obesity. Obesity affects about 125 million people in the United States 41.9% of adults and 19.7% of children and adolescents. Notably, 90% of people with diabetes also live with overweight or obesity. Weight gain is a major problem for physicians and patients looking to achieve adequate glycemic, blood pressure and lipid control in patients with diabetes.

"Over the past few years, we have seen the substantial impact of new research working to solve the dual health crisis we are facing, obesity and diabetes," said Dr. Robert Gabbay, chief scientific and medical officer for the ADA. "The studies we are seeing presented at this year's annual meeting show great promise to fuel new solutions and treatment options for patients across the globe living with type 2 diabetes and obesity."

Drug Treatment for Obesity Effectively Reduces Body Weightand Blood Pressure

HRS9531 is a dual GLP-1/GIP (glucose-dependent insulinotropic polypeptide) receptor agonist, offering a treatment option for individuals with overweight or obesity, as well as type 2 diabetes. This Phase 2 study evaluated the efficacy and safety of HRS9531 in obese adults without diabetes. The research found HRS9531 effectively reduced body weight, blood pressure, blood glucose, and triglycerides, with a favorable safety profile.

The double-blind, randomized, placebo-controlled Phase 2 trial studied a total of 249 Chinese adults with a body mass index of 28-40 kg/m. Participants were randomized into five groups to receive once-weekly subcutaneous injections of HRS9531 (1.0 mg, 3.0 mg, 4.5 mg, and 6.0 mg) or placebo for 24 weeks. The primary endpoint was the percentage change in body weight at week 24.

Greater weight loss was achieved in individuals receiving HRS9531 compared with those receiving placebo. At the end of the 24-week intervention, participants in 1.0 mg, 3.0 mg, 4.5 mg, and 6.0 mg HRS9531 groups achieved weight reductions of 5.4%, 13.4%, 14.0%, and 16.8% respectively, as compared with 0.1% reduction in the placebo group. Moreover, the proportion of participants achieving 5% weight reduction was 52.0%, 88.2%, 92.0%, 91.8%, and 10.2%, respectively. Most adverse events (AEs) were mild or moderate, and the most common AEs were nausea, diarrhea, decreased appetite, and vomiting, occurring primarily during dose escalation. The overall safety and tolerability profile of HRS9531 is consistent with other GLP-1 agonists.

"People living with obesity are at a high risk of developing chronic diseases such as type 2 diabetes and cardiovascular disease. Losing weight significantly reduces the risk of those diseases," said Xiaoying Li, MD, PhD. Professor and Director, Department of Endocrinology and Metabolism, Zhongshan Hospital Fudan University, China, and senior author. "Since dietary and exercise intervention alone is often not enough, we were pleased to see that this could be a potentially promising treatment for weight management, potentially enhancing their overall health and significantly reducing the societal burden of obesity."

The authors of the study note a Phase 3 study with HRS9531 in Chinese overweight or obese individuals is already ongoing and multi-regional studies are being planned.

Experimental Medication, Pemvidutide, Reveals 15.6% Average Total Body Weight Loss for Patients with Overweight and Obesity

The Phase 2 MOMENTUM trial evaluated the potential for pemvidutide, Altimmune's investigational medication, a GLP-1/Glucagon dual receptor agonist, in development for obesity and a liver disease called metabolic-dysfunction associated steatohepatitis (MASH), to help people with overweight and obesity lose weight. The trial revealed promising results - significantly reducing body weight and serum lipids over 48 weeks of treatment. In addition, body composition analysis demonstrated class-leading preservation of lean mass.

This Phase 2, randomized, placebo-controlled trial enrolled 391 subjects with overweight or obesity, but without diabetes, and administered either pemvidutide at three dose levels (1.2, 1.8, 2.4 mg) or a placebo weekly for 48 weeks. Neither the investigators nor the subjects knew what treatment they were receiving.

After 48 weeks, subjects at the highest pemvidutide dose had lost an average of 15.6% of their total body weight, and the treatment appeared to be safe and well-tolerated. Several potential advantages of this approach to weight loss were identified, including a simple dosing regimen and significant decreases in the amount of lipids (such as cholesterol and triglycerides) present in the blood and the liver, which may help reduce the risk of cardiovascular disease. Additionally, results from a body composition sub-study were presented indicating class-leading preservation of lean mass, with only 21.9% attributable to lean mass and 78.1% of weight loss due to fat. Preserving lean mass, which primarily includes muscle, is believed to be critical for maintaining physical function and decreasing the risk of bone fractures.

"Obesity and its associated comorbidities represent a major and growing health challenge. A variety of therapeutic approaches will be required to meet the specific needs of each patient to effectively manage their weight and address other obesity-related conditions they may have," said Louis J. Aronne, MD, FACP, DABOM, Weill Cornell Medicine, New York City, NY, and primary investigator. "These findings demonstrated that the use of pemvidutide may have important effects on the quality of weight loss and cardiometabolic-associated comorbidities of obesity. Furthermore, as the focus shifts to long-term weight management, the preservation of lean mass will be critical for patient care."

The authors of this study are preparing for larger Phase 3 registrational trials intended to demonstrate the safety and clinical benefit of pemvidutide for weight management. In addition, because obesity can lead to the accumulation of excess liver fat and MASH, they are also studying pemvidutide in patients with this condition.

Retatrutide Improves Ability of Insulin to Lower Blood Sugar for People Living with Type 2 Diabetes

Biomarker analyses may help in the understanding of diseases and identifying specific therapeutic targets. A new study evaluated biomarkers to observe how treatment with retatrutide affects pancreatic beta cells that make insulin as well as biomarkers associated with the body's ability to respond to insulin to lower blood sugar. In this study, exploratory biomarker research within phase 2 clinical trials was examined to further understand on the molecular level how retatrutide may work and further help explain primary results.

The research found treatment with retatrutide increased markers of well-functioning insulin-producing beta cells (HOMA2-B) and the ability of insulin to lower blood sugar (adiponectin). The results also demonstrated how retatrutide decreased markers of stress on insulin-producing cells, as assessed by measuring immature insulin (proinsulin) and reduction in a marker of insulin resistance (HOMA2-IR).

"This study matters because many people living with type 2 diabetes are taking multiple diabetes medications to try to reach blood sugar targets, and new medications that have the potential to help simplify treatment regimens are needed," said Melissa K. Thomas, MD, PhD, Vice President, Diabetes and Metabolic Research, Lilly Research Laboratories, Indianapolis, IN, and one of the investigators conducting the study. "We are encouraged to see that people living with either obesity or with type 2 diabetes in our clinical studies had lowered blood sugar and had improved responses to insulin."

Several Phase 3 clinical trials are underway studying retatrutide in people living with type 2 diabetes or obesity without type 2 diabetes including the TRIUMPH and TRANSCEND Phase 3 trials.

Research presentation details:

Dr.Zeng will present the findings at the following late-breaking poster session:

Dr. Aronne will present the findings at the following presentation session:

Dr. Thomas will present the findings at the following oral presentation session:

About the ADA's Scientific SessionsThe ADA's 84th Scientific Sessions, the world's largest scientific meeting focused on diabetes research, prevention, and care, will be held in Orlando, FL on June 21-24. More than 11,000 leading physicians, scientists, and health care professionals from around the world are expected to convene both in person and virtually to unveil cutting-edge research, treatment recommendations, and advances toward a cure for diabetes. Attendees will receive exclusive access to thousands of original research presentations and take part in provocative and engaging exchanges with leading diabetes experts. Join the Scientific Sessions conversation on social media using #ADAScientificSessions.

About the American Diabetes AssociationThe American Diabetes Association (ADA) is the nation's leading voluntary health organization fighting to bend the curve on the diabetes epidemic and help people living with diabetes thrive. For 83 years, the ADA has driven discovery and research to treat, manage, and prevent diabetes while working relentlessly for a cure. Through advocacy, program development, and education we aim to improve the quality of life for the over 136 million Americans living with diabetes or prediabetes. Diabetes has brought us together. What we do next will make us Connected for Life. To learn more or to get involved, visit us atdiabetes.orgor call 1-800-DIABETES (1-800-342-2383). Join the fight with us on Facebook (American Diabetes Association), Spanish Facebook (Asociacin Americana de la Diabetes), LinkedIn (American Diabetes Association), Twitter (@AmDiabetesAssn), and Instagram (@AmDiabetesAssn).

Media Contact: Amy Robinson [emailprotected]

SOURCE American Diabetes Association

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The relationship between SARS-CoV-2 infection and type 1 diabetes mellitus – Nature.com

Posted: June 24, 2024 at 2:39 am

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Prevalence of peripheral neuropathy, amputation, and quality of life in patients with diabetes mellitus | Scientific Reports – Nature.com

Posted: June 24, 2024 at 2:39 am

A cross-sectional observational study was conducted on 225 patients (42.2% males and 57.8% females) with type I (2.2%) and type II DM (97.8%), having a diabetic history of fewer than five years in 56% of participants of age ranging from 35-70 years, The study aimed to scrutinize the prevalence of peripheral neuropathy and amputation in patients with DM and evaluate their quality of life by utilizing the Michigan Neuropathy Screening Instrument and the Asian Diabetic Quality of Life Questionnaire. The levels of amputation from toe amputations to hemipelvectomy were observed.

Martin CL et al. in 2014 found that the most common of these neuropathic disorders is chronic diabetic peripheral sensorimotor neuropathy (DPN), which affects up to 50% of persons with DM14. The study's findings revealed a significant prevalence of peripheral neuropathy among the participants, emphasizing the considerable burden of this complication in patients with DM. Our study conducted on 225 patients with DM demonstrates the prevalence of DNP (diabetic peripheral neuropathy) using the Michigan neuropathy screening instrument (MNSI) self-administer questionnaire (SAQ) was 44.4% and 51.1% on the basis of the lower extremity examination part of the MNSI. Whereas, 55.6% and 48.9% were observed for the population without DPN using SAQ and the physical examination part of MNSI, respectively. Peripheral neuropathy is a well-recognized consequence of DM, characterized by nerve damage that can lead to various sensory and motor deficits, including pain, tingling, numbness, loss of sensation, muscle weakness, and impaired balance. The high prevalence rate underscores the need for early detection and effective management strategies to prevent or mitigate its adverse effects on patients well-being.

Hazari et al. (2023) reported that the risk of DPN is ethnic origin-dependent in residents of the United Arab Emirates and is high in Arab-origin residents. According to the findings of MNSI, 62% of the participants were screened with DPN28. The current study's findings are in line with their results in terms of DPN on the basis of MNSI but are limited in terms of information regarding the ethnicity and geographical background of the participants.

Amputation, another severe complication associated with DM, was also found to be prevalent in the study sample. This outcome raises concerns about the impact of DM on vascular health and underscores the significance of comprehensive diabetic foot care programs. Amputations can have profound physical, psychological, and social implications for individuals, leading to long-term disability and reduced quality of life. The identification of factors such as age, duration of DM, and glycemic control as predictors of peripheral neuropathy and amputation provides valuable insights for risk stratification and targeted interventions. In this study, the prevalence of amputations observed in patients with DM in the right and left lower limb are 0.4% and 0% hemipelvectomy, respectively, with short above knee amputation being 0.4%, 2.2%, respectively, standard below the knee in 9.8%, 3.6% respectively, toe disarticulation or amputation in 2.7%, 1.8 respectively, and Symes being 0.4% in both lower limbs. Baumfeld D et al. in 2018 found that in Pakistan, the rate of amputation (number of amputations due to diabetes per year) has been reported to be 21%-48%, despite the prevalence of diabetic foot ulcerations that is comparable to that of other countries29. The total rate of amputation, according to our study among the sample population, is 21.7%, which is similar to other research done before.

Furthermore, the study demonstrated the quality of life of the participants. This finding highlights the multidimensional nature of quality of life and the significant impact that these complications have on various aspects of a patient's well-being. According to the results of our study, DPN and amputation may have a negative association with four components of Asian DQOL in patients with DM. Our study showed that 96.9% of the population had poor QOL (score<45), 2.2% had moderate QOL (score 4550), and 0.9% had good QOL (score 5055). The study concluded results for four components of the Asian DQOL questionnaire with lower scores indicating poor QOL and vice versa. Total energy score 83.6% with (scores of 04) 14.7%, and 1.8% (scores 58 and 912, respectively), total memory scores 04, 58, 912, and 1316 with 30.0%, 34.7%, 20.9%, and 14.2% respectively, total finance score 05, 610, 1115, and 1620 with 51.1%, 39.6%, 6.7%, and 2.7% respectively, and total diet score of 04, 58, 912 with 67.1%, 30.2%, and 2.7% respectively. The mean energy score is 2.811.82 out of 12, which seems to be very low; the mean memory score is 7.974.53 out of 16, appearing as less than half of the total score, mean finance score is 6.384.34 out of 20 which is also very poor, mean diet score is 3.772.17 out of 12 and total score is 20.9510.40 out of 60. Most of the results depict poor quality of life in the study population.

Physical functioning is often compromised due to the sensory and motor deficits associated with peripheral neuropathy, limiting mobility and impairing daily activities. Psychological well-being is affected by chronic pain, anxiety, depression, and the psychological adjustment to the loss of a limb in the case of amputation. Social interactions may also be impacted as individuals may experience social stigma, reduced participation in social activities, and a sense of isolation. Overall, life satisfaction is significantly diminished as a result of the limitations imposed by these complications. According to our findings, numerous studies from different countries have indicated that type II DM has a detrimental effect on QOL30,31,32,33.

While this study provides valuable insights into the prevalence of peripheral neuropathy, amputation, and quality of life in patients with DM, it is important to acknowledge certain limitations. The cross-sectional design of this study limits the ability to establish causal relationships between variables. Longitudinal studies would be beneficial in determining temporal relationships and understanding the long-term effects of these complications.

Healthcare providers should prioritize early detection and screening of peripheral neuropathy in patients with Diabetic mellitus. A multidisciplinary approach involving healthcare professionals from various specialities, such as endocrinology, podiatry, and physical therapy, is recommended, along with long-term follow-up. Collaboration among these specialists can provide comprehensive care, including education, foot care guidance, wound management, and rehabilitation services for individuals with peripheral neuropathy or amputation. Recognizing the impact of peripheral neuropathy and amputation on the quality of life, healthcare providers should offer psychological support and rehabilitation services to affected patients. Access to counselling, prosthetics and mobility aids can help individuals cope with the physical, emotional, and social challenges associated with these complications.

The present study had a few limitations which need to be mentioned here. The study's sample was drawn from patients attending a specific healthcare facility, which may introduce sampling bias and limit the generalizability of the findings to a broader population. Patients seeking care at these facilities may have different characteristics or access to healthcare compared to the general population. Individuals with concurrent chronic illnesses like heart disease, cancer, or renal disorders, with a history of trauma, severe psychiatric conditions, or addiction were excluded due to some ethical limitation. This prevented the analysis from having external validity. Many patients have multiple comorbidities, and it is difficult for neuropathy to be the only complication.

Only MNSI was used, and it could not be compared with nerve conduction study, which is a gold standard for diagnosing patients with peripheral neuropathy. Due to ethical considerations, the interpersonal relationship component of Asian DQOL was not included in this study. The study relied on self-reported data, which was subjected to recall bias. Patients may have inaccurately reported their medical history, symptoms, or quality of life. Additionally, subjective assessments of QoL may be influenced by individual perceptions and experiences.

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What to Know About Cannabis Use and Diabetes, with Halis Akturk, MD – MD Magazine

Posted: June 24, 2024 at 2:39 am

Despite medical cannabis in the US dating back more than 3 decades, the legalization movement in the last decade means millions and millions of US adults now have access to cannabis, for both medical and recreational purposes.

However, with this boom in use, concerns regarding the health effects of cannabis use have become a greater focal point of discussion among medical circles. According to a 2023 study in JAMA Network Open, 17% of a 175,000-patient cohort of adults reported cannabis use in the previous 3 months and 34.7% of those individuals met the criteria for moderate to high risk for cannabis use disorder.1

At the 84th American Diabetes Association Scientific Sessions, Halis Akturk, MD, associate professor of medicine and pediatrics at the Barbara Davis Center for Diabetes at the University of Colorado, led a session titled The Highs and Lows of Cannabis Use in DiabetesBehavioral and Psychosocial Considerations. Based in Colorado, Akturk has a unique view from the frontlines of research and real-world practice as Colorado was among the first states to allow for both medical and nonmedical cannabis use.

In the past 5 years, Akturk has published numerous studies detailing the effects of cannabis use with type 1 diabetes. In 2019, a study from Akturk in JAMA Internal Medicine evidenced the elevated risk of diabetic ketoacidosis among adults with type 1 diabetes using cannabis receiving care at the Barbara Davis Center for Diabetes. Building o this research, a similar study published in Diabetes Care in 2020 confirmed a similar trend using data from the T1D Exchange clinical registry. In 2022, Akturk led an additional study providing clinicians with an overview of the differences in presentation between diabetic ketoacidosis and hyperglycemic ketosis due to cannabis hyperemesis syndrome.2,3,4

At ADA 2024, we sat down with Akturk to learn more about this emerging space, what additional risks are associated with cannabis use in adults with and without type 1 diabetes, and what questions hears most often from his colleague regarding the topic.

HCPLive: What is the prevalence of cannabis use among people with type 1 diabetes and what are the primary reasons cited for use?

Akturk: In Colorado, we have the one of the highest rates of cannabis users with type one diabetes. So, we did a survey study a couple years ago and we asked the adults with type one diabetes: "Have you been using the cannabis or have you ever used the cannabis in the last 12 months?". In the results, there were about 30% of the patients in the adult clinic with type 1 diabetes that were at least used once cannabis in the last one year. The reasons for use were multiple, with about 75% of the people were using recreational reasons and 25% of the people were using medicinal reasons. In some states, you can just get a medicinal card for different indications. This was relatively a high use in our community for type 1 diabetes.

HCPLive: What are some of the chief concerns about how the effects of cannabis use manifest among patients with type 1 diabetes?

Akturk: Our previous research showed that the people who are using cannabis have an increased risk for diabetic ketoacidosis when they have type 1 diabetes. This was a local study we did a couple of years ago in JAMA, where we were trying to find out the reasons for that. Then we went to the T1D Exchange data and we looked to see if we can confirm our study results. We confirmed that the people who are using cannabis, after adjustment for the other things like pump use, age, diabetes, duration and other confounders, were at an increased for diabetic ketoacidosis.

As a next step, we realized that these people have a different the metabolic profile when they present to ER with the diabetic ketoacidosis symptoms. In other research, what we did is we looked at their metabolic profiles and their labs to compared people who are using cannabis and not using it. So, we did an objective study, and we looked at their urine drug screen use. If somebody's urine drug screen is positive for cannabis, we consider this person is using and, if it's not that, we consider that as not using it.

We found very significant differences in terms of the labs at presentation. We showed that these same people are also getting hyperglycemia, they are getting ketosis, and they have an onion gap. They also present to the ER with nausea and vomiting. But the main difference was the pH and the bicarb. So, their pH was more than 7.4 and their bicarb was more than 15. So, in DKA, there should be pH should be less than 7.3 and bicarb should be less than 15. So, we call them as a different entity, as hyperglycemic ketosis related to the cannabis hyperemesis syndrome.

HCPLive: When should providers approach discussions around cannabis use among patients with type 1 diabetes?

Akturk: I think we should educate people about cannabis at the type 1 diabetes diagnosis. We have a structured plan for the sick day management for alcohol and we added structures for cannabis education in the type 1 diabetes care program at the Barbara Davis Center. If there is a new patient, I suggest the providers, especially the endocrinologist, to discuss the cannabis with them at their first visit. If they have some frequent visits related to the ER visits and there are some frequent diabetic ketosis episodes, I suggest asking them if they use cannabis or not.

Editor's note: these transcripts have been edited for length and clarity.

Disclosures of interest for Akturk include REMD, Dexcom, Senseonics, and Eli Lilly and Company.

References:

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Exploratory risk prediction of type II diabetes with isolation forests and novel biomarkers | Scientific Reports – Nature.com

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Diabetes Research Institute Announces Breakthrough Transplantation Approach for the Treatment of Type 1 Diabetes … – University of Miami

Posted: June 24, 2024 at 2:39 am

By: Staff Writer | June 21, 2024 | 5 min. read| Share Article Summary

The Diabetes Research Institute (DRI) at the University of Miami Miller School of Medicine unveiled an innovative approach at the American Diabetes Associations (ADA) 84th Scientific Sessions that highlights the potential of human, stem cell-derived islets combined with an immunomodulatory microgel to reverse Type 1 diabetes (T1D).

This technology was developed to enable pancreatic islet cell replacement in the allogeneic setting (from a donor to an unrelated recipient) without the need for chronic, systemic immunosuppression.

The collaborative effort was spearheaded by Giacomo Lanzoni, Ph.D., a Miller School research assistant professor in biochemistry and molecular biology, with teams from iTolerance, Inc., and Kadimastem, Ltd. The research demonstrates that the combination of iTOL-100 engineered microgel developed by iTolerance, Inc., and IsletRx stem cell-derived islets developed by Kadimastem, Ltd., can effectively restore normoglycemia in a model of diabetes.

Our observations highlight the transformative potential of combining stem cell-derived islets with an immunomodulatory microgel, Dr. Lanzoni said. This approach could enable transplantation across the allogeneic barrier, offering a scalable and sustainable solution for T1D, and could enhance the safety and long-term efficacy of islet cell transplantation.

The Fast Track Center for Testing at the DRI Cell Transplant Center continues to serve as a key shared resource to validate emerging technologies towards a cure for diabetes, said Camillo Ricordi, M.D., director of the Cell Transplant Center and director emeritus at the Diabetes Research Institute as well as chief in the Division of Cellular Transplantation at the Miller School. We hope to continue to be of assistance towards the identification of reliable and potentially unlimited stem cell-derived islet sources for transplantation, which may one day be able to replace the limited availability of pancreas-derived islets from multiorgan donors, when lifelong recipient immunosuppression will no longer be required.

The studys key findings indicate that this combination therapy reverses diabetes and preserves the functional integrity of the transplanted stem cell-derived islets.

iTOL-100, an immunomodulatory microgel designed to eliminate the need for chronic systemic immunosuppression and shown to induce local immune acceptance of transplanted islets, was found to be compatible with stem cell-derived islets.

IsletRx, a preparation of human, stem cell-derived islets, is a scalable and virtually unlimited source of insulin-producing cells and could address the critical shortage of donor islets for transplantation.

The transplantation procedure is performed in a retrievable site, ensuring the possibility of graft retrieval through a minimally invasive surgery, if needed.

The study reports reversal of disease in a chemically induced model of diabetes, with comparable efficacy of IsletRx in the presence or absence of iTOL-100, indicating a lack of toxicity from the microgel.

iTolerance is pleased to co-sponsor the project at the Diabetes Research Institute toward a functional cure of T1D through the combination of human stem cell-derived insulin producing islet cells together with our iTOL-100 proprietary immunomodulator, said Anthony Japour, M.D., CEO of iTolerance, Inc. Removing the need for life-long toxic immunosuppressive agents in islet transplantation is a common goal among those working toward a cure for T1D through transplantation without immunosuppression.

Our collaboration with iTolerance opens an innovative and world-first avenue for transplanting pancreatic islet cells into people with diabetes without the need for full suppression of the immune system, which is required today in organ transplants, said Michel Revel, M.D., Ph.D., chief scientist at Kadimastem, Ltd. Our company produces high-quality pancreatic islet cells. The joint data collected by us proves the possibility of combining our cells with the material that locally prevents the rejection of the implant developed by our project partner iTolerance. Having successfully completed an Interact meeting with the FDA, the two companies are moving together to the pre-IND submission stage.

IsletRx is comprised of clinical-grade clusters of human pancreatic islet like cells (ILCs) with the ability to secrete insulin. IsletRx cells can detect the sugar levels in the body and produce the required amounts of insulin and glucagon. The companys technology can select and enrich only the highest functioning and purest islet cells from the population of pluripotent stem cells, which enables the maximum therapeutic effect.

The project was supported in part by iTolerance, Inc., Kadimastem, Ltd., grants funded by the Breakthrough T1D Foundation (formerly known as JDRF) and the Israel-U.S. Binational Industrial Research (BIRD) Foundation.

Tags: Camillo Ricordi, diabetes, Diabetes Research Institute, DRI, giacomo lanzoni, islet cell transplantation, pancreas

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Diabetes Research Institute Announces Breakthrough Transplantation Approach for the Treatment of Type 1 Diabetes ... - University of Miami

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New MiniMed 780G system data demonstrates ability to address persistent blood sugar challenges for people with … – PR Newswire

Posted: June 24, 2024 at 2:39 am

With its advanced algorithm that provides autocorrections every 5 minutes, the latest data demonstrated that the MiniMed 780G system decreased rates of early morning hyperglycemia, known asdawn phenomenon, and improved overnight sleep

DUBLIN and ORLANDO, Fla., June 21, 2024 /PRNewswire/ -- Medtronic plc(NYSE: MDT),a global leader in healthcare technology, is presenting a comprehensive body of new data at the American Diabetes Association's (ADA) 84thScientific Sessions that showcases the benefits of the MiniMed 780G system. New data shows how the system addresses hyperglycemia and nighttime burden, adding to the established body of evidence that demonstrates the system's ability to tackle unique and burdensome challenges of diabetes, such as managing highs and meal-time management or carb counting, while also mirroring outcomes across a wide-ranging patient population.

Tackling hyperglycemia to improve long-term health with type 1 diabetesAmong the burdens of living with diabetes, hyperglycemia can often be overshadowed by hypoglycemia. Yet, in the U.S., only 26% of people living with diabetes achieve HbA1c levels of <7.0%.1Reducing the time spent with high blood sugars continues to be a significant unmet need as it can lead to serious health problems impacting multiple organs.2 For children, prolonged highscan have adverse effects on memory, IQ, executivefunctioning, and learning.3

One cause of high blood sugars is the dawn phenomenon, an increase in glucose levels in the early morning.4 This can be a common occurrence for those living with diabetes and may add to feelings of frustration with diabetes. An encouraging new retrospective analysis of real-world data (n= 6026) showed that this morning peak was nearly eliminated for users who upgraded from the MiniMed 770G system to the MiniMed 780G system. The data assessed the elevation of sensor glucose levels >20 mg/dL from 3 - 6 a.m. compared to 12 3 a.m. at least 30% of the nights. The transition from the MiniMed 770G system to the MiniMed 780G system decreased dawn phenomenon rates from 12.2% to 4.5%. Time in Range also increased from 87.7% to 91.4% from 12 6 a.m., which is consistent with dawn phenomenon trends.

Early and consistent management of hyperglycemia is critical as it has protective effects on the body that can last for decades.5 "For those living with type 1 diabetes, dawn phenomenon can be a stressful occurrence that feels out of one's control," explained Robert Vigersky, MD, Chief Medical Officer, Medtronic Diabetes. "The introduction of the MiniMed 780G system has made it easier to maintain target glucose range with less effort to protect against hyperglycemia.6,7 It's been an absolute gift for my patients who have struggled with stubborn highs throughout their diabetes journey."

Reducing nighttime burden For individuals living with type 1 diabetes, CGM-generated alerts and the need to deliver manual boluses disrupt sleeping through the night adding to the burden of diabetes. The MiniMed 780G system is designed to reduce the burden of diabetes throughout the day and night. Additional real-world data from a retrospective analysis presented at ADA (n=8019; <7 y/o, previously on the MiniMed 770G system who had greater than 14 nights on both systems) demonstrated that users had fewer overnight sleep interruptions and Time in Range improvements as a result of the automatic adjustments in insulin and correction of glucose levels every 5 minutes, including during sleep. With the MiniMed 780G system, nighttime alerts decreased 45% for all users and 55% for those who used recommended optimal settings. Additionally, uninterrupted sleep, a greatly desired outcome for those living with diabetes, increased by 30 and 36 minutes per night, respectively. These results add to the diabetes burden reduction that MiniMed 780G system users experience with an advanced algorithm with frequent, every 5-minute autocorrections.

The continued evolution of the MiniMed 780G system to reduce burdenAlong with evidence on the currently available MiniMed 780G system, additional data will be presented on the next iteration of the system,* which aims to further reduce diabetes management burden through its design. The system is intended to be paired with the Simplera Sync sensor, a disposable, all-in-one continuous glucose monitor (CGM) designed to require no overtape.

A 24-site, single arm study evaluated the use of the next iteration of the MiniMed 780G system algorithm paired with the Simplera Sync sensor. Results were promising across all clinical outcomes metrics including Time in Range (TIR), Time in Tight Range (TITR) and Time Above Range (TAR), compared to the run-in group where hybrid closed loop (auto basal only) or open-loop delivery was used. The study included the use of recommended optimal settings (ROS) (100 mg/dL set target with an active insulin time of 2 hours) related to TIR, TITR, and TAR.

"The MiniMed 780G system has firmly established itself as a proven automated insulin delivery system," said study investigator Gregory Forlenza, MD, professor and pediatric endocrinologist at the Barbara Davis Center. "With the next iteration of the system and this next-generation Simplera Sync sensor, the overall experience for people living with type 1 diabetes could be enhanced and may prove to be a compelling option for diabetes management particularly when leveraged in combination with recommended optimal settings."

The MiniMed 780G system** is currently available for ages 7 and above in over 100 countries globally and will be launching with the Simplera Sync sensor in parts of Europe in late July. Currently, Simplera Sync is investigational and not approved for commercial use in the U.S.*

Safety and Glycemic Outcomes Using the MiniMed 780G system with an All-in-One Disposable Sensor with Transmitter 3-month study period (n=109, ages 7-17; n=107, ages 18-80)

Youths

(ages 7-17)

Adults

(ages 18-80)

Run-in (N=112)

Study (N=109)

ROS (N=41)

Run-in (N=110)

Study (N=107)

ROS (N=44)

Time in Smart Guard, %

14.531.3

93.511.3

96.93.1

33.240.3

96.66.6

97.53.7

Mean SG, mg/dL

180.427.1

154.417.6

149.015.3

161.018.7

142.212.8

136.512.0

Percentage of time spent at glucose ranges

<70 mg/dL

(% TBR)

1.61.7

1.91.4

1.91.2

1.71.9

1.51.4

1.71.4

70-140 mg/dL

(% TITR)

32.114.1

49.29.7

52.79.2

39.213.0

56.110.5

61.69.9

70-180 mg/dL

(% TIR)

54.415.7

71.49.9

74.79.3

66.512.6

80.28.1

83.87.4

>180 mg/dL

(% TAR)

44.016.1

26.710.1

23.39.4

31.813.1

18.28.4

14.57.7

Caption: Glycemic metrics and insulin delivered during youth and adult MiniMed 780G system investigational use with the disposable all-in-one Simplera Sync sensor

To view this data at the 84thAmerican Diabetes Association (ADA) Scientific Sessions inOrlando, Florida, view the company's previous announcement here for presentation times.

About MedtronicBold thinking. Bolder actions. We are Medtronic. Medtronic plc, headquartered in Dublin, Ireland, is the leading global healthcare technology company that boldly attacks the most challenging health problems facing humanity by searching out and finding solutions. Our Mission to alleviate pain, restore health, and extend life unites a global team of 95,000+ passionate people across more than 150 countries. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world. In everything we do, we are engineering the extraordinary. For more information on Medtronic, visit http://www.Medtronic.com and follow Medtronic on LinkedIn.

About Medtronic Diabetes (www.medtronicdiabetes.com) Medtronic Diabetes is on a mission to alleviate the burden of diabetes by empowering individuals to live life on their terms, with the most advanced diabetes technology and always-on support when and how they need it. We've pioneered first-of-its-kind innovations for over 40 years and are committed to designing the future of diabetes management through next-generation sensors (CGM), intelligent dosing systems, and the power of data science and AI while always putting the customer experience at the forefront.

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.

*Investigational. Not approved by the FDA for any use and not commercially available in the US.

**MiniMed 780G system is for type 1 ages 7 and over. Prescription required. WARNING: Do not use SmartGuard feature for people who require less than 8 units or more than 250 units of insulin/day. For details, seehttps://bit.ly/780gRisks

Refers to auto correct, which provides bolus assistance. Can deliver all auto correction doses automatically without user interaction, feature can be turned on and off.

Refers toSmartGuard feature. Individual results may vary.

Contacts:

Ashley Patterson

RyanWeispfenning

Public Relations

Investor Relations

+1 (818) 576-3025

+1 (763) 505-4626

SOURCE Medtronic plc

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