Abbasi Laraib, Irfan Qunoot, Zaidi Syed Muhammad Mehdi, Jawed Izma, Malik Abdullah, Kaleem Shamama
Dow Medical College, Dow University of Health Science, Karachi, Sindh, Pakistan.
Eur J Gastroenterol Hepatol. 2025 Apr 1;37(4):395-402. doi: 10.1097/MEG.0000000000002901. Epub 2024 Dec 3.
Metabolic dysfunction-associated steatohepatitis (MASH) affects nearly 38% of the population, potentially progressing to cirrhosis and cancer. Lifestyle changes remain the cornerstone of management, but adherence is challenging, prompting the exploration of therapeutic options. Resmetirom, targeting thyroid hormone receptors, regulates liver enzymes and fat metabolism, showing potential as a treatment for MASH. This systematic review and meta-analysis evaluates the safety of resmetirom in MASH patients. Three randomized controlled trials with adult participants were analyzed, sourced from PubMed and the Cochrane Library until April 2024. Participants received either resmetirom or placebo, and data on adverse effects and efficacy outcomes were extracted. Statistical analyses, including risk ratios (RRs) and confidence intervals (CI), were performed using Review Manager (version 5.4.1) with a random-effects model. The pooled RR for serious adverse events was 0.85 (95% CI: 0.63-1.14; P = 0.28), indicating no significant difference. However, diarrhea (RR = 1.82, 95% CI: 1.41-2.35; P < 0.001) and nausea (RR = 1.73, 95% CI: 1.31-2.28; P < 0.001) showed higher incidence. No significant differences were found for fatigue (RR = 1.19, 95% CI: 0.77-1.84; P = 0.43) or urinary tract infections (RR = 1.07, 95% CI: 0.76-1.52; P = 0.69). Liver fat content, lipid profiles, and liver enzymes also showed significant improvement in the resmetirom group. Low heterogeneity across most outcomes indicated consistent findings among the studies. While resmetirom demonstrates efficacy in improving lipid and liver profiles, its increased risk of diarrhea and nausea should be considered in therapeutic decisions.
代谢功能障碍相关脂肪性肝炎(MASH)影响着近38%的人口,有发展为肝硬化和癌症的潜在风险。生活方式的改变仍然是治疗的基石,但坚持下去具有挑战性,这促使人们探索治疗方案。Resmetirom靶向甲状腺激素受体,可调节肝脏酶和脂肪代谢,显示出作为MASH治疗方法的潜力。本系统评价和荟萃分析评估了Resmetirom在MASH患者中的安全性。分析了三项针对成年参与者的随机对照试验,数据来源为截至2024年4月的PubMed和Cochrane图书馆。参与者接受Resmetirom或安慰剂治疗,并提取了不良反应和疗效结果的数据。使用Review Manager(版本5.4.1)和随机效应模型进行统计分析,包括风险比(RRs)和置信区间(CI)。严重不良事件的合并RR为0.85(95%CI:0.63 - 1.14;P = 0.28),表明无显著差异。然而,腹泻(RR = 1.82,95%CI:1.41 - 2.35;P < 0.001)和恶心(RR = 1.73,95%CI:1.31 - 2.28;P < 0.001)的发生率较高。疲劳(RR = 1.19,95%CI:0.77 - 1.84;P = 0.43)或尿路感染(RR = 1.07,95%CI:0.76 - 1.52;P = 0.69)未发现显著差异。Resmetirom组的肝脏脂肪含量、血脂谱和肝酶也有显著改善。大多数结果的低异质性表明各研究结果一致。虽然Resmetirom在改善脂质和肝脏指标方面显示出疗效,但在治疗决策中应考虑其腹泻和恶心风险增加的问题。