Opinion: American horses are obese, too

The horses in America are getting fat. They are trying to tell us something.

Fifty-one percent of mature light-breed horses in the United States are obese — a rate that ranks among the world’s highest, slightly above Britain and nearly twice that of Australia or Denmark. That figure comes from a peer-reviewed prevalence study, and it sits alongside a number that should give any clinician pause: The U.S. also leads the G7 in human obesity. The same country. The same epidemic. A completely different species.

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Survodutide in adults with obesity and metabolic dysfunction-associated steatotic liver disease: SYNCHRONIZE-MASLD, a randomized, double-blind, placebo-controlled phase 3 trial

Nature Medicine, Published online: 07 June 2026; doi:10.1038/s41591-026-04479-3

As presented at the American Diabetes Association Meeting, in this phase 3 trial, weekly subcutaneous injections of survodutide, a glucagon receptor/GLP-1R dual agonist, lowered liver fat content and body weight compared to placebo in adults with obesity and at-risk metabolic dysfunction-associated steatotic liver disease (MASLD).

STAT+: Competition for obesity drugs, clinical blind spots, and more news from ADA

You’re reading the web edition of STAT’s ADA in 30 Seconds newsletter, from the American Diabetes Association’s annual conference. 

Welcome to the third and final edition of STAT’s ADA in 30 Seconds newsletter.

Elaine Chen starts us off with updates on the competitive climate for obesity drugs and I’m relaying insights on eating disorders, new word on a BCG vaccine, and a clarification from ADA on Friday’s police incident.

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STAT+: New data may cast doubt on competitiveness of Boehringer’s obesity drug

New data on Boehringer Ingelheim’s obesity candidate suggest the drug may be helpful in cutting liver fat, but it’s not clear how competitive the treatment would be since it appears less efficacious and less tolerable than drugs on the market.

In a Phase 3 obesity trial, patients on the highest dose of the weekly injectable, called survodutide, lost 13% of their weight after 76 weeks, compared with 5% in the placebo group, according to data presented Sunday at the annual meeting of the American Diabetes Association and published in the New England Journal of Medicine. That’s lower than the rate of weight loss seen in pivotal trials of Novo Nordisk’s Wegovy and Eli Lilly’s Zepbound. 

Patients on survodutide, which targets the GLP-1 and glucagon hormones, did lose up to 63% of their liver fat, compared with 25% in the placebo group. Glucagon-targeting drugs are thought to be particularly helpful in cutting liver fat, since there are glucagon receptors in the liver.

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STAT+: Lilly shares safety, tolerability data on its next-gen obesity drug

Eli Lilly has already established that its next-generation obesity drug can lead to highly rapid weight loss. Researchers disclosed new data Saturday that provide more details on the safety and tolerability of the closely-watched therapy.

Lilly previously said that in one late-stage study, called TRANSCEND-T2D-1, retatrutide helped people with diabetes lower blood sugar and lose a significant amount of weight, which is notable since those who have diabetes tend to lose less weight on treatment than those who don’t.

New data showed that seven out of the 403 participants who received retatrutide experienced arrhythmias (irregular heart beats), and three treated participants experienced major cardiovascular complications, compared with none in the placebo group. The data were presented at the annual meeting of the American Diabetes Association and published in the Lancet.

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GLP-1 Drugs Lower Risk of Death by 44% in Obesity and Autoimmune Disease

An analysis of electronic health records from over 26,000 adults with obesity and at least one autoimmune disease has shown that those taking GLP-1 medication experienced fewer cardiac events, were less likely to visit the ER, and had a lower risk of death. These findings were published today in the Journal of the American Heart Association and presented at the American Diabetes Association 2026 Scientific Sessions in New Orleans. 

“This is a high-risk population, and historically we’ve had limited data to guide treatment decisions,” said Amy Sheer, MD, associate professor of medicine and director of the Obesity Medicine Fellowship program at the University of Florida. “In this real-world analysis, we found a consistent signal toward fewer serious complications including blood clots and lower mortality among patients treated with GLP-1 receptor agonists. For people who are overweight or living with obesity and an autoimmune disease, this study offers a hopeful signal that medications already in use today may be beneficial in reducing their risk of cardiovascular disease.”

GLP-1 receptor agonists are commonly prescribed drugs to help patients with type 2 diabetes lose weight and manage their blood sugar levels. This study is the first to examine the potential cardiovascular benefits of these drugs in a high-risk population of patients with both obesity and an autoimmune disease—both of which are associated with a higher risk of cardiovascular and blood clot events. 

Sheer and colleagues reviewed electronic health record data from 26,408 adults treated in the OneFlorida+ network from 2014 to 2024, covering 14 healthcare organizations across Florida, Georgia, and Alabama. Half of the patients were taking GLP-1 drugs over this 10 year period, while the other half did not. 

Across this population, GLP-1 treatment was found to reduce the risk of blood clots by 17%, of pulmonary embolism by 31%, and of death by 44%. Visits to the emergency department were also lowered by 21%, and a modest decrease in stroke risk of 13% was also found. 

“The 44% reduction in all-cause mortality observed among patients with obesity and co-occurring autoimmune disease is a striking finding that demands our attention,” said Fatima Cody Stanford, MD, associate professor of medicine and pediatrics at Harvard Medical School, who was not involved in the study. “As an obesity medicine physician scientist who regularly cares for patients with complex inflammatory conditions, this study reinforces what many of us have suspected clinically—that the benefits of GLP-1 receptor agonists extend well beyond blood sugar control and weight loss and may fundamentally alter the disease trajectory for some of our highest-risk patients.”

Although this study cannot prove a causal link between GLP-1 medication and the effects seen on the patients taking them, it opens the door to future combinations of treatments for autoimmune disease with GLP-1 drugs. More research is still needed to understand the role this medication could play as a potential preventive therapy for high-risk patients.

“Our research broadens the conversation around GLP-1 receptor agonists,” said Sheer. “For clinicians, we hope these findings may prompt a more thoughtful, individualized approach when considering these therapies in higher-risk patients who have both obesity and autoimmune disease.”

The post GLP-1 Drugs Lower Risk of Death by 44% in Obesity and Autoimmune Disease appeared first on Inside Precision Medicine.

STAT+: Detailed data show Pfizer’s monthly obesity drug continues to show potential

Detailed data from a mid-stage study offered further evidence that the obesity drug Pfizer acquired from the biotech Metsera could be dosed monthly. But it’s not clear how competitive the treatment would be against weekly injectables on the market and in development that may lead to greater weight loss.

In the study, called VESPER-3, patients with obesity took weekly doses of the drug, called berobenatide, for 12 weeks and then transitioned to higher monthly doses out to 28 weeks. By then, patients lost up to 12.1% of their weight, when analyzing just those who stayed on treatment, as Pfizer previously reported. 

New data presented at the annual meeting of the American Diabetes Association on Saturday show that when patients transitioned from weekly to monthly dosing, the rate of weight loss continued at a similar pace; they had not yet hit a plateau by 28 weeks. That’s a promising sign, but the rate of weight loss at 28 weeks was still less than what was seen at a similar time point in the pivotal trial of Eli Lilly’s Zepbound.

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Oral small molecule GLP-1 receptor agonist aleniglipron in people with overweight or obesity: a randomized, double-blind, placebo-controlled phase 2b trial

Nature Medicine, Published online: 05 June 2026; doi:10.1038/s41591-026-04476-6

As presented at the American Diabetes Association Meeting: this randomized phase 2b trial in 230 adults with overweight or obesity shows that aleniglipron, an oral small-molecule GLP1-RA, led to up to 11.3% body-weight loss compared with placebo after 36 weeks of treatment.