非酒精性脂肪性肝炎患者服用雷美替罗的疗效和安全性:系统回顾和元分析

Saad Mazhar, Aima Azhar, Ariba Khan, Gulrukh Shakil, Deepa Devi, Sapna Kumari, Sayed Jawad
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引用次数: 0

摘要

非酒精性脂肪性肝炎(NASH)是一种严重的内科疾病,可供选择的治疗方案很少。甲状腺激素受体(THR)的肝脏靶向激动剂雷美替罗最近获得了美国食品药品管理局(FDA)的许可。我们评估了雷美替罗对非酒精性脂肪性肝炎(NASH)患者的有效性和安全性。 我们对 PubMed、SCOPUS 和 Cochrane Central 进行了检索,直至 2024 年 3 月才找到可能的文章。评估的结果包括 MRI-PDFF、脂肪减少、无纤维化的 NASH 解体、谷草转氨酶(AST)、谷丙转氨酶(ALT)、谷草转氨酶(GGT)、低密度脂蛋白(LDL)和甘油三酯(TG)水平的变化,以及腹泻、恶心、UTI 和头痛。对 6 个月前和 6 个月后的结果进行了分组分析。结果采用随机效应模型进行分析,连续性结果以平均差(MD)表示,安全性分析结果以几率比(OR)表示,并列出其 95% 的置信区间。偏倚风险评估采用 Cochrane 偏倚风险工具进行。 我们在分析中纳入了四项研究。Resmetirom对MRI-PDFF有显著改善,平均差异为-19.23(P<0.00001)。此外,它还使脂肪减少了 30%(几率比:3.54,P=0.004),并解决了 NASH 无纤维化的问题(几率比:2.41,P=0.04)。在谷草转氨酶水平方面没有观察到明显的改善,平均差异为-0.87,P 值为 0.73。使用瑞美替罗后,ALT 水平(平均差异:-4.36,P 值:0.32)、GGT 水平(平均差异:-17.87,P 值:<0.00001)、TG 水平(平均差异:-23.48,P 值:<0.00001)、LDL 水平(平均差异:-12.80,P 值:<0.00001)和 rT3 水平(平均差异:-2.08,P 值:<0.00001)均有显著改善。使用 Resmetirom 会增加腹泻(几率比 [OR]:2.07,P<0.0001)和恶心(OR:1.81,P=0.0003)的可能性。不过,在尿路感染(UTI)(OR:1.04,P=0.85)或头痛(OR:0.79,P=0.48)的发生率方面没有观察到明显差异。 Resmetirom 在提高 NASH 患者的 MRI-PDFF 评分、减少脂肪组织、缓解 NASH 但无纤维化、降低 GGT、TG、LDL 和 rT3 水平方面具有疗效。不过,也观察到该药物会增加腹泻和恶心的易感性。有必要进行更多试验,以进一步研究这种药物的疗效和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of resmetirom among patients with Non-alcoholic steatohepatitis: a systematic review and Meta-Analysis
Nonalcoholic steatohepatitis (NASH) is a severe medical illness that has few available therapeutic options. Resmetirom, a liver-targeting agonist of the thyroid hormone receptor (THR), has recently been licenced by the FDA. We assess the effectiveness and safety of resmetirom in patients with non-alcoholic steatohepatitis (NASH). PubMed, SCOPUS and Cochrane Central were searched till March 2024 to find potential articles. Outcomes assessed included MRI-PDFF, Fat Reduction, and NASH Resolution Without Fibrosis, changes in AST, ALT, GGT, LDL, and triglyceride (TG) levels, along with diarrhea, nausea, UTI, and headache. Subgroup analysis was performed between outcomes before and after 6 months. Outcomes were analyzed with random effects model and results presented as mean difference (MD) for continuous outcomes and odds ratios (OR) for safety analysis, along with their 95% confidence intervals. Risk of bias assessment was performed using Cochrane Risk of Bias tool. Four RCTs were included in our analysis. Resmetirom shown a substantial improvement in MRI-PDFF with a mean difference of -19.23 (P<0.00001). Additionally, it resulted in a 30% reduction in fat (odds ratio: 3.54, P=0.004) and resolution of NASH without fibrosis (odds ratio: 2.41, P=0.04). There was no notable enhancement observed in AST levels, with a mean difference of -0.87 and a P-value of 0.73. The usage of resmetirom resulted in significant improvement in ALT levels (mean difference: -4.36, P-value: 0.32), GGT levels (mean difference: -17.87, P-value: <0.00001), TG levels (mean difference: -23.48, P-value: <0.00001), LDL levels (mean difference: -12.80, P-value: <0.00001), and rT3 levels (mean difference: -2.08, P-value: <0.00001). The use of Resmetirom was associated with a higher likelihood of experiencing diarrhea (odds ratio [OR]: 2.07, P<0.0001) and nausea (OR: 1.81, P=0.0003). However, there was no significant difference observed in the occurrence of urinary tract infections (UTI) (OR: 1.04, P=0.85) or headaches (OR: 0.79, P=0.48). Resmetirom demonstrates efficacy in enhancing MRI-PDFF score, diminishing adipose tissue, resolving NASH without fibrosis, reducing GGT, TG, LDL, rT3 levels in NASH patients. Nevertheless, there is also an observed heightened susceptibility to experiencing diarrhea and nausea. Additional trials are necessary to further examine the efficacy and safety of this medication.
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