Department of Gastroenterology, ILS Dumdum Hospital, Kolkata 700 080, India.
Department of Clinical and Experimental Pharmacology, Calcutta School of Tropical Medicine, Kolkata, India.
Clin Res Hepatol Gastroenterol. 2023 Aug;47(7):102174. doi: 10.1016/j.clinre.2023.102174. Epub 2023 Jun 26.
This systematic review and meta-analysis was conducted to evaluate the efficacy and safety of 4 mg saroglitazar treatment in patients with non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH).
PubMed, Embase, Scopus, Cochrane CENTRAL, medRxiv (pre-print), bioRxiv (pre-print), and ClinicalTrials.gov databases were searched for relevant studies. The primary outcome was the change in the serum alanine transaminase (ALT) level. The secondary outcomes were changes in liver stiffness, liver function test parameters, and metabolic parameters. Pooled mean differences were calculated using random-effects models.
Of 331 studies that were screened, ten were included. Treatment with adjunct saroglitazar showed a reduction in ALT [mean difference: 26.01 U/L (95% CI: 10.67 to 41.35); p = 0.009; i: 98%; moderate GRADE evidence] and aspartate transaminase [mean difference: 19.68 U/L (95% CI: 8.93 to 30.43); p<0.001; i: 97%; moderate GRADE evidence] levels. There was a significant improvement in liver stiffness [mean difference: 2.22 kPa (95% CI: 0.80 to 3.63); p = 0.002; i: 99%; moderate GRADE evidence]. There were significant improvements in glycated hemoglobin [mean difference: 0.59% (95% CI: 0.32 to 0.86); p<0.001; i: 78%; moderate GRADE evidence], total cholesterol [mean difference: 19.20 (95% CI: 1.54 to 36.87); p = 0.03; i: 95%; moderate GRADE evidence], and triglyceride [mean difference: 105.49 mg/dL (95% CI: 11.18 to 199.80); p = 0.03; i: 100%; moderate GRADE evidence] levels. Saroglitazar treatment was safe.
Treatment with adjunct 4 mg saroglitazar could significantly improve liver enzymes, reduce liver stiffness, and improve metabolic parameters (serum glucose and lipid profile) in patients with NAFLD or NASH.
本系统评价和荟萃分析旨在评估 4mg 沙格列汀治疗非酒精性脂肪性肝病(NAFLD)或非酒精性脂肪性肝炎(NASH)患者的疗效和安全性。
检索了 PubMed、Embase、Scopus、Cochrane 中心、medRxiv(预印本)、bioRxiv(预印本)和 ClinicalTrials.gov 数据库中相关研究。主要结局是血清丙氨酸氨基转移酶(ALT)水平的变化。次要结局是肝硬度、肝功能试验参数和代谢参数的变化。使用随机效应模型计算汇总均数差异。
在筛选出的 331 项研究中,有 10 项研究被纳入。辅助沙格列汀治疗可降低 ALT[平均差异:26.01U/L(95%CI:10.67 至 41.35);p=0.009;I²:98%;中等级别证据]和天门冬氨酸氨基转移酶[平均差异:19.68U/L(95%CI:8.93 至 30.43);p<0.001;I²:97%;中等级别证据]水平。肝硬度显著改善[平均差异:2.22kPa(95%CI:0.80 至 3.63);p=0.002;I²:99%;中等级别证据]。糖化血红蛋白[平均差异:0.59%(95%CI:0.32 至 0.86);p<0.001;I²:78%;中等级别证据]、总胆固醇[平均差异:19.20(95%CI:1.54 至 36.87);p=0.03;I²:95%;中等级别证据]和甘油三酯[平均差异:105.49mg/dL(95%CI:11.18 至 199.80);p=0.03;I²:100%;中等级别证据]水平均有显著改善。沙格列汀治疗是安全的。
辅助应用 4mg 沙格列汀治疗可显著改善 NAFLD 或 NASH 患者的肝功能,降低肝硬度,并改善代谢参数(血糖和血脂谱)。