Gao Zhenxiang, Tabernacki Tomasz, Dorney Ian, Ding Pingjian, Kaelber David C, Xu Rong
Center for Artificial Intelligence in Drug Discovery, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Acta Diabetol. 2025 Jun 5. doi: 10.1007/s00592-025-02525-z.
Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are approved for treating type 2 diabetes and weight loss. There have been concerns that GLP-1RAs may increase the risk of intestinal obstruction.
Investigate the association between GLP-1RAs use and intestinal obstruction in a large cohort of patients with type 2 diabetes mellitus (T2DM) in the U.S.
A retrospective cohort study was conducted using longitudinal electronic health records sourced from TriNetX, a large-scale, population-based health database.
The study included over 1.2 million T2DM patients who were prescribed anti-diabetic medications, including 181,795 prescribed GLP-1RAs between April 2013 and April 2019.
The incidence of intestinal obstruction was compared between GLP-1RAs and each of six other classes of non-GLP-1RA anti-diabetic medications. Hazard ratios (HRs) at 1, 3, and 5-year follow-up periods were calculated using Cox proportional hazards analysis. Separate analyses were performed in T2DM patients with and without obesity.
The risk of intestinal obstruction did not differ between GLP-1RAs and other anti-diabetic medications except for a reduced risk compared with insulins. The results were consistent for 1, 3, and 5-year follow-up periods and in patients with and without obesity.
Our findings do not support an increased risk of intestinal obstruction in T2DM patients prescribed GLP-1 RAs compared to other anti-diabetic medications.
胰高血糖素样肽-1受体激动剂(GLP-1RAs)已被批准用于治疗2型糖尿病和减肥。人们一直担心GLP-1RAs可能会增加肠梗阻的风险。
在美国一大群2型糖尿病(T2DM)患者中调查GLP-1RAs的使用与肠梗阻之间的关联。
使用来自TriNetX的纵向电子健康记录进行了一项回顾性队列研究,TriNetX是一个大规模的、基于人群的健康数据库。
该研究纳入了超过120万开具抗糖尿病药物的T2DM患者,其中包括2013年4月至2019年4月期间开具GLP-1RAs的181,795名患者。
比较了GLP-1RAs与其他六类非GLP-1RAs抗糖尿病药物中每一类的肠梗阻发生率。使用Cox比例风险分析计算1年、3年和5年随访期的风险比(HRs)。在有肥胖和无肥胖的T2DM患者中进行了单独分析。
除了与胰岛素相比风险降低外,GLP-1RAs与其他抗糖尿病药物之间的肠梗阻风险没有差异。1年、3年和5年随访期以及有肥胖和无肥胖的患者结果一致。
我们的研究结果不支持与其他抗糖尿病药物相比,开具GLP-1RAs的T2DM患者肠梗阻风险增加。