Effects of GLP-1 receptor agonist therapy on resolution of steatohepatitis in non-alcoholic fatty liver disease: a systematic review and meta-analysis.

IF 2.7
Journal of the Canadian Association of Gastroenterology Pub Date : 2025-01-29 eCollection Date: 2025-04-01 DOI:10.1093/jcag/gwae057
Kathryn J Potter, Jackie Phinney, Tasha Kulai, Vicki Munro
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Abstract

Background: Non-alcoholic fatty liver disease (NAFLD) is common, can progress to cirrhosis and hepatic decompensation, and has no approved medical therapy in Canada.

Objective: We conducted a systematic review on whether glucagon-like peptide-1 receptor agonists (GLP-1RA) improve non-alcoholic steatohepatitis (NASH) compared to standard care in NAFLD.

Methods: We searched Medline Ovid, EMBASE(Elsevier), Cochrane CENTRAL, Clinical Trials.gov, and the World Health Organization International Clinical Trials Registry Platform in November 2023 for randomized controlled trials. Inclusion criteria included patients ≥13 years with NAFLD receiving GLP-1RA for ≥6 months compared to standard care/placebo. Cochrane risk-of-bias 2.0 tool was used for each outcome. After screening results in duplicate, we performed meta-analysis and reported odds ratios (OR) for dichotomous and mean difference of change score for continuous outcomes.

Results: Six studies with 478 patients met inclusion criteria; 3 studies reported on the primary endpoint resolution of NASH. GLP-1RA likely leads to resolution of NASH (OR 4.45 (95% CI 1.92, 10.3)) and reduction in liver steatosis on imaging (-5.09% (95% CI -7.49, -2.69), but little to no reduction in liver stiffness on imaging (mean difference -0.17 kPa (95% CI -0.34, 0)).

Interpretation: Treatment with GLP-1RA in NAFLD patients for ≥6 months can probably lead to improvement in NASH on liver biopsy and reduce liver steatosis on imaging. Whether improvements in steatosis on biopsy or imaging results in clinically significant outcomes need to be elucidated as the effects of GLP-1RA on liver fibrosis are unclear; larger ongoing trials may provide more definitive answers. Protocol Registration: PROSPERO-CRD42023472186.

GLP-1受体激动剂治疗对非酒精性脂肪性肝炎患者脂肪性肝炎的疗效:一项系统综述和荟萃分析
背景:非酒精性脂肪性肝病(NAFLD)很常见,可发展为肝硬化和肝功能失代偿,在加拿大尚无批准的药物治疗。目的:我们对胰高血糖素样肽-1受体激动剂(GLP-1RA)与标准治疗相比是否能改善非酒精性脂肪性肝炎(NASH)进行了系统回顾。方法:我们于2023年11月检索Medline Ovid、EMBASE(Elsevier)、Cochrane CENTRAL、Clinical Trials.gov和世界卫生组织国际临床试验注册平台进行随机对照试验。纳入标准包括≥13年的NAFLD患者,与标准治疗/安慰剂相比,接受GLP-1RA治疗≥6个月。每个结果使用Cochrane风险偏倚2.0工具。在重复筛选结果后,我们进行了荟萃分析,并报告了连续结果的二分类和平均变化评分差异的优势比(OR)。结果:6项研究478例患者符合纳入标准;3项研究报道了NASH的主要终点解决方案。GLP-1RA可能导致NASH的分辨率(OR 4.45 (95% CI 1.92, 10.3))和影像学上肝脏脂肪变性的降低(-5.09% (95% CI -7.49, -2.69),但影像学上肝脏僵硬程度几乎没有降低(平均差值-0.17 kPa (95% CI -0.34, 0))。解释:GLP-1RA治疗NAFLD患者≥6个月可能导致肝活检显示NASH改善,影像学显示肝脂肪变性减少。由于GLP-1RA对肝纤维化的影响尚不清楚,因此需要阐明活检或影像学上脂肪变性的改善是否会导致临床显著结果;正在进行的更大规模的试验可能会提供更明确的答案。协议注册:PROSPERO-CRD42023472186。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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