| アブストラクト | BACKGROUND: Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), medications used to treat type 2 diabetes and obesity, are associated with delayed gastric emptying, which is a risk factor for gastroesophageal reflux disease (GERD). However, evidence linking these drugs to GERD is limited. OBJECTIVE: To estimate the effect of GLP-1 RAs compared with sodium-glucose cotransporter-2 (SGLT-2) inhibitors on the risk for GERD and its complications among patients with type 2 diabetes. DESIGN: Active-comparator new-user cohort study emulating a target trial. SETTING: U.K. Clinical Practice Research Datalink. PARTICIPANTS: Adults aged 18 years or older with type 2 diabetes initiating GLP-1 RAs or SGLT-2 inhibitors between 1 January 2013 and 31 December 2021, with follow-up until 31 March 2022. MEASUREMENTS: The primary outcome was incident GERD, and the secondary outcome was its complications. Three-year risk differences (RDs) and risk ratios (RRs) were estimated and weighted using propensity score fine stratification. RESULTS: The study included 24 708 new users of GLP-1 RAs and 89 096 new users of SGLT-2 inhibitors. Over a median follow-up of 3.0 years, the RRs were 1.27 (95% CI, 1.14 to 1.42) for GERD, with an RD of 0.7 per 100 patients, and 1.55 (95% CI, 1.12 to 2.29) for its complications, with an RD of 0.8 per 1000 patients, among GLP-1 RA users compared with SGLT-2 inhibitor users. LIMITATION: Residual confounding due to lack of information on dietary or lifestyle factors. CONCLUSION: The estimated effect of GLP-1 RAs compared with SGLT-2 inhibitors suggested a higher risk for GERD and its complications in patients with type 2 diabetes. Clinicians should be aware of this potential adverse effect to provide timely prevention and treatment strategies. PRIMARY FUNDING SOURCE: Canadian Institutes of Health Research. |
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| ジャーナル名 | Annals of internal medicine |
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| Pubmed追加日 | 2025/7/14 |
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| 投稿者 | Noh, Yunha; Yin, Hui; Yu, Oriana H Y; Bitton, Alain; Azoulay, Laurent |
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| 組織名 | College of Pharmacy, Chonnam National University, Gwangju, South Korea (Y.N.).;Center for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital,;Montreal, Quebec, Canada (H.Y.).;Division of Endocrinology, Jewish General Hospital, Montreal, Quebec, Canada;(O.H.Y.Y.).;Division of Gastroenterology, McGill University Health Centre, Montreal, Quebec,;Canada (A.B.).;Department of Epidemiology, Biostatistics and Occupational Health, McGill;University; Center for Clinical Epidemiology, Lady Davis Institute, Jewish;General Hospital; and Gerald Bronfman Department of Oncology, McGill University,;Montreal, Quebec, Canada (L.A.). |
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| Pubmed リンク | https://www.ncbi.nlm.nih.gov/pubmed/40658955/ |
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