奥贝胆酸(一种类法内酯 X 受体激动剂)在非酒精性脂肪肝中的作用:系统综述与元分析》。

TouchREVIEWS in endocrinology Pub Date : 2024-10-01 Epub Date: 2024-10-09 DOI:10.17925/EE.2024.20.2.8
Abm Kamrul-Hasan, Sunetra Mondal, Lakshmi Nagendra, Thanikai Sasikanth, Afsar Ahammed, Shahin Ibn Rahman, Ashani Wickramarachchi, Naresh Parajuli, Saurav Khatiwada, Deep Dutta
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引用次数: 0

摘要

背景。奥贝胆酸(OCA)已成为治疗非酒精性脂肪肝(NAFLD)的一种有前途的药物。本荟萃分析旨在分析奥贝胆酸对非酒精性脂肪肝的治疗效果。方法:随机对照试验在电子数据库中搜索了非酒精性脂肪肝患者在干预组接受OCA治疗、在对照组接受安慰剂治疗的随机对照试验(RCT)。主要结果是非侵入性肝纤维化标志物和肝组织学的变化。次要结果包括肝酶、代谢参数与基线相比的变化以及不良事件(AEs)。研究结果有四项研究符合纳入标准,涉及 1,278 名受试者。临床使用 6 周至 18 个月期间,OCA 在缓解明确的非酒精性脂肪性肝炎(几率比 [OR] 1.60,95% 置信区间 [CI] [1.04-2.48],P=0.03)和改善肝纤维化(OR 2.23,95% CI [1.56-3.20],P=0.03)方面优于安慰剂。奥卡因在改善肝组织学和肝酶方面疗效显著。然而,使用奥卡因后血脂参数和其他AEs的恶化值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Obeticholic Acid, a Farnesoid X Receptor Agonist, in Nonalcoholic Fatty Liver Disease: A Systematic Review and Meta-analysis.

Background. Obeticholic acid (OCA) has emerged as a promising drug in the management of nonalcoholic fatty liver disease (NAFLD). This meta-analysis aimed to analyse the therapeutic effect of OCA on NAFLD. Methods. Randomized controlled trials (RCTs) involving patients with NAFLD receiving OCA in the intervention arm and placebo in the control arm were searched throughout the electronic databases. The primary outcomes were changes in non-invasive markers of hepatic fibrosis and liver histology. The secondary outcomes included changes in liver enzymes, metabolic parameters from baseline and adverse events (AEs). Results. Four RCTs involving 1,278 subjects met the inclusion criteria. Over 6 weeks to 18 months of clinical use, OCA outperformed placebo in resolving definite nonalcoholic steatohepatitis (odds ratio [OR] 1.60, 95% confidence interval [CI] [1.04-2.48], p=0.03) and improving fibrosis (OR 2.23, 95% CI [1.56-3.20], p<0.0001), hepatocellular ballooning (OR 1.83, 95% CI [1.35-2.47], p<0.0001) and lobular inflammation (OR 1.62, 95% CI [1.13-2.32], p=0.009). OCA did not improve the enhanced liver fibrosis score and steatosis better than placebo, and demonstrated superior efficacy compared with the placebo in reducing serum alanine aminotransferase, aspartate aminotransferase and gamma-glutamyl transferase levels. Although a favourable effect of OCA over placebo was seen in body-weight reduction, the OCA use was associated with adverse changes in lipid parameters. Except for the greater risk of pruritus and constipation, the AE profile was comparable between the OCA and placebo groups. Conclusions. OCA has a favourable efficacy in improving liver histology and liver enzymes. However, the worsening of lipid parameters and other AEs with the OCA use warrants further investigation.

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