Recent research from the University of British Columbia has found that GLP-1 agonists, a type of diabetes medication used off-label for weight loss, carry heightened risks of severe gastrointestinal complications. The study, which looked into non-diabetic patients using these drugs for weight loss, found increased risks of pancreatitis, bowel obstruction, and gastroparesis. Although these events are rare, given the vast number of users worldwide, many could still be affected. Researchers advocate for clearer warning labels to ensure patients are fully informed.
They’re being hailed as an effective way to lose weight, but diabetes drugs like Ozempic may come with a heightened risk of severe gastrointestinal problems.
That’s according to new research from the University of British Columbia showing that medications known as GLP-1 agonists—which includes brands like Wegovy, Ozempic, Rybelsus, and Saxenda—are associated with an increased risk of serious medical conditions including stomach paralysis, pancreatitis, and bowel obstruction.
Findings in Non-diabetic Patients
While previous studies highlighted some of these risks in patients with diabetes, this is the first large, population-level study to examine adverse gastrointestinal events in non-diabetic patients using the drugs specifically for weight loss. The findings were published today in JAMA.
“Given the wide use of these drugs, these adverse events, although rare, must be considered by patients thinking about using them for weight loss,” said first author Mohit Sodhi, a graduate of UBC’s experimental medicine program and fourth-year UBC medical student studying the adverse events of commonly prescribed medications. “The risk calculus will differ depending on whether a patient is using these drugs for diabetes, obesity, or just general weight loss. People who are otherwise healthy may be less willing to accept these potentially serious adverse events.”
Rise in Off-label Use
First author Mohit Sodhi of the University of British Columbia. Credit: UBC Faculty of Medicine
GLP-1 agonists were originally developed for managing Type 2 diabetes, but exploded in popularity over the past decade as an off-label weight-loss tool, reaching approximately 40 million prescriptions in the U.S. in 2022.
It was only in 2021 that some forms of the medications were approved as a treatment for obesity. However, randomized clinical trials examining the efficacy of the medications for weight loss were not designed to capture rare gastrointestinal events due to their small sample sizes and short follow-up periods.
“There have been anecdotal reports of some patients using these drugs for weight loss and then presenting with repeated episodes of nausea and vomiting secondary to a condition referred to as gastroparesis,” said senior author Dr. Mahyar Etminan, an epidemiologist and associate professor in the department of ophthalmology and visual sciences at the UBC faculty of medicine. “But until now, there hasn’t been any data from large epidemiologic studies.”
Detailed Study Findings
To help fill this knowledge gap, UBC researchers examined health insurance claim records for approximately 16 million U.S. patients and looked at people prescribed either semaglutide or liraglutide, two main GLP-1 agonists, between 2006 and 2020. They included patients with a recent history of obesity, and excluded those with diabetes or who had been prescribed another antidiabetic drug.
The researchers analyzed the records to see how many patients developed one of four gastrointestinal conditions and compared that rate to patients using another weight loss drug, bupropion-naltrexone. Compared to bupropion-naltrexone, GLP-1 agonists were associated with a:
- 9.09 times higher risk of pancreatitis, or inflammation of the pancreas, which can cause severe abdominal pain and, in some cases, require hospitalization and surgery.
- 4.22 times higher risk of bowel obstruction, whereby food is prevented from passing through the small or large intestine, resulting in symptoms like cramping, bloating, nausea, and vomiting. Depending on the severity, surgery may be required.
- 3.67 times higher risk of gastroparesis, or stomach paralysis, which limits the passage of food from the stomach to the small intestine and results in symptoms like vomiting, nausea, and abdominal pain.
The study also found a higher incidence of biliary disease, a group of conditions affecting the gall bladder, but the difference was not found to be statistically significant.
Implications and Recommendations
The researchers say that although the events are rare, with millions around the world using the drugs, it could still lead to hundreds of thousands of people experiencing these conditions.
“These drugs are becoming increasingly accessible, and it is concerning that, in some cases, people can simply go online and order these kinds of medications when they may not have a full understanding of what could potentially happen. This goes directly against the mantra of informed consent,” said Sodhi.
In the meantime, the researchers hope that regulatory agencies and drug makers will consider updating the warning labels for their products, which currently don’t include the risk of gastroparesis.
“This is critical information for patients to know so they can seek timely medical attention and avoid serious consequences,” said Sodhi.
Reference: “Risk of Gastrointestinal Adverse Events Associated With Glucagon-Like Peptide-1 Receptor Agonists for Weight Loss” by Mohit Sodhi, Ramin Rezaeianzadeh, Abbas Kezouh and Mahyar Etminan, 5 October 2023, JAMA.
DOI: 10.1001/jama.2023.19574
The pancreatitis risk was known and is on the label. The gastropariesis risk was discovered maybe 6 months ago, and the FDA recently added it to the label. It’s good the risks are being clarified.
I’m convinced there will be other risks discovered. Medicating such a large population inevitably turns up more risks, and the history of weightloss drugs is a pattern of popularity then recalls. If I were to speculate, for example, I imagine the slow digestion would increase bowel cancer risk. Still, I’m excited about the progress.
Shouldn’t the mere fact that GLP-1 agonists cause the increase in insulin level, in and of itself, be a concern?
We still can’t fool Mother Nature. Even at $1200 per month forever. Billions more each month for big pharma, enormous insurance premium increases for the rest of us. God forbid that people might eat less and walk more.