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Heart benefits fade after stopping GLP-1 medications
A study of over 333,000 adults found that stopping GLP-1 drugs like Ozempic raises cardiovascular risk, reversing benefits gained from continuous use over three years.
- Published on Wednesday in BMJ Medicine, a Washington University School of Medicine study found short gaps in GLP-1 treatment raise risks of heart attack, stroke and death, tracking more than 333,000 adults with Type 2 diabetes, mostly on Novo Nordisk's Ozempic.
- Roughly one in eight U.S. adults take GLP-1 drugs, but discontinuation rates run as high as 36% to 81% due to access problems and side effects like nausea and vomiting.
- Analysis showed quitting for six months raised risk by 4% and a two-year gap pushed it to 22%, while patients who stayed on GLP-1s saw an 18% reduction in cardiovascular risk, Washington University said.
- Al-Aly warned that stopping GLP-1s causes cardiovascular protection to vanish, calling it a 'metabolic whiplash' and urging providers and patients to stay on treatment 'for the long haul'.
- Policy moves such as Medicare covering weight-loss drugs could ease access, as Eli Lilly pursues employer-coverage efforts and drugmakers develop next-generation treatments with fewer side effects.
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Stopping GLP-1 Drugs Can Quickly Erase Cardiovascular Benefits
WashU Medicine researchers found that stopping GLP-1 drugs such as semaglutide and tirzepatide — even temporarily — elevates the risk of heart attack, stroke and death compared to staying on the medication continuously.
·Charlottesville, United States
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Total News Sources31
Leaning Left1Leaning Right0Center28Last UpdatedBias Distribution97% Center
Bias Distribution
- 97% of the sources are Center
97% Center
C 97%
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