Safety and efficacy of liraglutide on reducing visceral and ectopic fat in adults with or without type 2 diabetes mellitus: A systematic review and meta‐analysis

利拉鲁肽 医学 内科学 2型糖尿病 子群分析 体质指数 荟萃分析 随机对照试验 置信区间 不利影响 糖尿病 2型糖尿病 内分泌学 胃肠病学
作者
Fengling He,Wei Chen,Wenlong Xu,Dan Liu,Zhiwen Xiao,Yating Tang,Zhongqiu Lin,Yulin Liao,Jianping Bin,GuoJun Chen,Yanmei Chen
出处
期刊:Diabetes, Obesity and Metabolism [Wiley]
卷期号:25 (3): 664-674 被引量:9
标识
DOI:10.1111/dom.14908
摘要

Abstract Aim To assess the efficacy and safety of liraglutide to reduce visceral and ectopic fat in adults with or without type 2 diabetes mellitus (T2DM). Methods Four databases were searched up to 6 May 2022 for randomized clinical trials assessing the effect of liraglutide on visceral and ectopic fat. The mean and standard deviation of the values of visceral fat, ectopic fat and body mass index were calculated. Subgroup analyses were performed based on the type of disease (T2DM or non‐T2DM), duration of intervention, dosage of liraglutide and whether life interventions were added to liraglutide therapy. We extracted and integrated the safety assessments reported in each article. Results Sixteen randomized clinical trials with, in total, 845 participants were included in the meta‐analysis. Liraglutide could significantly decrease visceral fat [standard mean difference (SMD) = −0.72, 95% confidence interval (CI; −1.12, −0.33)], liver fat [SMD = −0.78, 95% CI (−1.24, −0.32)] and body mass index [weighted mean difference = −1.44, 95% CI (−1.95, −0.92)] in adult patients with or without T2DM when compared with the control group. However, reduction of epicardial fat by liraglutide [SMD = −0.74, 95% CI (−1.82, 0.34)] was not statistically significant. Subgroup analysis revealed that an adequate dosage (≥1.8 mg/day) and appropriate duration of treatment (ranging from 16 to 40 weeks) were the decisive factors for liraglutide to reduce visceral fat effectively. Mild gastrointestinal reactions were the main adverse event of liraglutide. Conclusions Liraglutide significantly and safely reduces visceral and ectopic liver fat irrespective of T2DM status, and reduces visceral fat provided adequate dosage and duration of therapy are ensured.
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