Ariyan Ayati, Iman Elahi Vahed, Yasaman Rahimi, Shima Karbasi, Ali Safdari, Mahkameh Razaghi, Aida Bazrgar, Melika Arab Bafrani, Mohammad Mehdi Mousavi Nasab, Masoud Noroozi, Shokoofeh Noori, Mohammad Rahmanian
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Searches of PubMed, Scopus, Web of Science, and Embase up to January 2025 were performed using specific keywords and MeSH terms. Bias assessment and data extraction were conducted using Joanna Briggs Institute (JBI) tools independently by two researchers. Statistical analyses were performed with Stata version 14, calculating standardized mean differences, 95% confidence intervals (CI), and heterogeneity (by performing Cochran's Q test and I<sup>2</sup> index). Moreover, meta-regression, subgroup analyses, and sensitivity analyses were conducted. Eleven studies featuring 582 participants were included. Orlistat treatment induced a significant reduction in levels of alanine transaminase (ALT) (SMD = -26.23; 95% CI = -34.70 to -17.76) and aspartate aminotransferase (AST) (SMD = -19.62; 95% CI = -28.33 to -10.92). Furthermore, reductions in HOMA-IR, body mass index, cholesterol, insulin, and waist circumference were observed. The included studies exhibited low to moderate heterogeneity for most outcomes, indicating consistent results across trials. Orlistat significantly improved AST, ALT, and some other metabolic parameters in MASLD patients, suggesting its potential as an additional treatment option. However, the outcome must be interpreted cautiously, considering study heterogeneity. 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引用次数: 0
摘要
代谢功能障碍相关脂肪变性肝病(MASLD)是一种与心血管疾病和代谢紊乱相关的持续性肝病。以肝内炎症、脂肪堆积和纤维化为特征,MASLD可发展为肝癌和肝硬化。全球患病率为32.4%,肥胖率也在上升。奥利司他抑制脂肪酶,因此,减少膳食脂肪吸收,这可能有利于MASLD患者。本系统评价和荟萃分析是按照PRISMA指南进行的。使用特定的关键词和MeSH术语对PubMed、Scopus、Web of Science和Embase进行了截至2025年1月的搜索。偏见评估和数据提取由两名研究人员独立使用乔安娜布里格斯研究所(JBI)的工具进行。采用Stata version 14进行统计分析,计算标准化平均差异、95%置信区间(CI)和异质性(通过Cochran’s Q检验和I2指数)。此外,还进行了meta回归、亚组分析和敏感性分析。纳入了11项研究,共有582名参与者。奥利司他治疗可显著降低丙氨酸转氨酶(ALT)水平(SMD = -26.23;95% CI = -34.70 ~ -17.76)和天冬氨酸转氨酶(AST) (SMD = -19.62;95% CI = -28.33 ~ -10.92)。此外,还观察到HOMA-IR、体重指数、胆固醇、胰岛素和腰围的降低。纳入的研究显示大多数结果具有低到中等的异质性,表明各试验的结果一致。奥利司他显著改善了MASLD患者的AST、ALT和其他一些代谢参数,表明它有可能作为一种额外的治疗选择。然而,考虑到研究的异质性,必须谨慎地解释结果。需要进一步的高质量、多中心研究来证实这些结果。
Efficacy of orlistat for the treatment of metabolic dysfunction-associated steatotic liver disease patients: A systematic review and meta-analysis.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a persistent hepatic condition linked with cardiovascular disorders and metabolic disturbances. Characterized by inflammation, fat accumulation, and fibrosis within the liver, MASLD can develop into liver cancer and cirrhosis. With a global prevalence of 32.4%, the condition parallels rising obesity rates. Orlistat inhibits lipase enzymes and, therefore, reduces dietary fat absorption, which may benefit MASLD patients. The present systematic review and meta-analysis were performed in accordance with PRISMA guidelines. Searches of PubMed, Scopus, Web of Science, and Embase up to January 2025 were performed using specific keywords and MeSH terms. Bias assessment and data extraction were conducted using Joanna Briggs Institute (JBI) tools independently by two researchers. Statistical analyses were performed with Stata version 14, calculating standardized mean differences, 95% confidence intervals (CI), and heterogeneity (by performing Cochran's Q test and I2 index). Moreover, meta-regression, subgroup analyses, and sensitivity analyses were conducted. Eleven studies featuring 582 participants were included. Orlistat treatment induced a significant reduction in levels of alanine transaminase (ALT) (SMD = -26.23; 95% CI = -34.70 to -17.76) and aspartate aminotransferase (AST) (SMD = -19.62; 95% CI = -28.33 to -10.92). Furthermore, reductions in HOMA-IR, body mass index, cholesterol, insulin, and waist circumference were observed. The included studies exhibited low to moderate heterogeneity for most outcomes, indicating consistent results across trials. Orlistat significantly improved AST, ALT, and some other metabolic parameters in MASLD patients, suggesting its potential as an additional treatment option. However, the outcome must be interpreted cautiously, considering study heterogeneity. Further high-quality, multicenter research is necessary to confirm these results.