Gastrointestinal adverse events of metformin treatment in patients with type 2 diabetes mellitus: A systematic review, meta-analysis and meta-regression of randomized controlled trials

二甲双胍 医学 元回归 内科学 2型糖尿病 不利影响 荟萃分析 随机对照试验 2型糖尿病 糖尿病 胰岛素 内分泌学
作者
Katarzyna Nabrdalik,Karolina Skonieczna‐Żydecka,Krzysztof Irlik,Mirela Hendel,Hanna Kwiendacz,Igor Łoniewski,Kornelia Januszkiewicz,Janusz Gumprecht,Gregory Y.H. Lip
出处
期刊:Frontiers in Endocrinology [Frontiers Media]
卷期号:13: 975912-975912 被引量:55
标识
DOI:10.3389/fendo.2022.975912
摘要

Introduction Metformin is the first choice drug in the treatment of type 2 diabetes mellitus but its administration may be linked to gastrointestinal adverse events limiting its use. Objectives The objective of this systematic review and meta-analysis was to assess the risk of gastrointestinal adverse events related to metformin use in patients with type 2 diabetes treated with metformin. Methods PUB MED/CINAHL/Web of Science/Scopus were searched from database inception until 08.11.2020 for articles in English and randomized controlled trials related to patients with type 2 diabetes treated with metformin were included. Results From 5315 publications, we identified 199 potentially eligible full-text articles. Finally, 71 randomized controlled trials were included in the meta-analysis. In these studies, metformin use was associated with higher risk of abdominal pain, diarrhea and nausea comparing to control. The risks of abdominal pain and nausea were highest comparing to placebo. Bloating risk was only elevated when metformin treatment was compared to DPP4i. Conclusions The risk of gastrointestinal adverse events such as abdominal pain, nausea and diarrhea is higher in type 2 diabetes patients treated with metformin compared to other antidiabetic drugs. There is a higher risk of bloating and diarrhea with metformin immediate-release than with metformin extended release formulation. Systematic Review Registration https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021289975 , identifier CRD42021289975.
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