Efficacy and safety of statins for nonalcoholic/metabolic dysfunction-associated fatty liver diseases: a systematic review and meta-analysis.

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Xiaohui Fang, Yuhang Yin, Qinke Wu, Lu Chai, Yifan Guo, Zhenhua Tong, Nahum Méndez-Sánchez, Xingshun Qi
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引用次数: 0

Abstract

Introduction: Nonalcoholic fatty liver diseases (NAFLD) and metabolic dysfunction-associated fatty liver diseases (MAFLD) are closely associated with metabolic syndrome, including obesity, dyslipidemia, and insulin resistance (IR). Thus, stains may be considered for the management of NAFLD/MAFLD. However, its efficacy and safety remain unclear in NAFLD/MAFLD.

Methods: The PubMed, EMBASE, and Cochrane library databases were searched to identify randomized controlled trials (RCTs) evaluating the efficacy and/or safety of statins in NAFLD/MAFLD. Risk ratios (RRs) and weight mean differences (WMDs) with their 95% confidence intervals (CIs) were calculated.

Results: Seven studies involving 993 patients with NAFLD/MAFLD were included. Statins were significantly associated with reductions in alanine aminotransferase (ALT, WMD = -9.76 U/L, 95%CI: -17.28, -2.24, p  = 0.010), aspartate aminotransferase (AST, WMD = -4.46 U/L, 95%CI: -9.03, 0.11, p  = 0.060), gamma-glutamyl-transpeptidase (GGT, WMD = -10.18 U/L, 95%CI: -13.65, -6.70, p  < 0.001), low-density lipoprotein (LDL, WMD = -0.86 mmol/L, 95%CI: -1.06, -0.66, p  < 0.001), total cholesterol (TC, WMD = -0.88 mmol/L, 95%CI: -1.14, -0.61, p  < 0.001), and triglyceride (TG, WMD = -0.32 mmol/L, 95%CI: -0.45, -0.19, p  < 0.001) levels. Additionally, statins did not increase the risk of myalgia (RR = 0.96, 95%CI: 0.10, 9.00, p  = 0.970).

Conclusions: Statins could improve liver function and lipid profiles in NAFLD/MAFLD. No myalgia was reported as AEs in the studies we included and the overall safety was favorable.Protocol registration: www.crd.york.ac.uk/prospero identifier is CRD42025630809.

他汀类药物治疗非酒精性/代谢功能障碍相关脂肪肝的疗效和安全性:一项系统综述和荟萃分析
非酒精性脂肪性肝病(NAFLD)和代谢功能障碍相关脂肪性肝病(MAFLD)与代谢综合征密切相关,包括肥胖、血脂异常和胰岛素抵抗(IR)。因此,可以考虑使用染色剂治疗NAFLD/MAFLD。然而,其在NAFLD/MAFLD中的疗效和安全性尚不清楚。方法:检索PubMed、EMBASE和Cochrane数据库,以确定评估他汀类药物治疗NAFLD/MAFLD疗效和/或安全性的随机对照试验(rct)。计算风险比(rr)和体重平均差(wmd)及其95%置信区间(ci)。结果:纳入7项研究,涉及993例NAFLD/MAFLD患者。他汀类药物可显著降低丙氨酸转氨酶(ALT, WMD = -9.76 U/L, 95%CI: -17.28, -2.24, P = 0.010)、天冬氨酸转氨酶(AST, WMD = -4.46 U/L, 95%CI: -9.03, 0.11, P = 0.060)、γ -谷氨酰转肽酶(GGT, WMD = -10.18 U/L, 95%CI: -13.65, -6.70, P)。结论:他汀类药物可改善NAFLD/MAFLD患者肝功能和血脂。在我们纳入的研究中没有肌痛被报道为不良反应,总体安全性是有利的。
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来源期刊
Expert Review of Clinical Pharmacology
Expert Review of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.30
自引率
2.30%
发文量
127
期刊介绍: Advances in drug development technologies are yielding innovative new therapies, from potentially lifesaving medicines to lifestyle products. In recent years, however, the cost of developing new drugs has soared, and concerns over drug resistance and pharmacoeconomics have come to the fore. Adverse reactions experienced at the clinical trial level serve as a constant reminder of the importance of rigorous safety and toxicity testing. Furthermore the advent of pharmacogenomics and ‘individualized’ approaches to therapy will demand a fresh approach to drug evaluation and healthcare delivery. Clinical Pharmacology provides an essential role in integrating the expertise of all of the specialists and players who are active in meeting such challenges in modern biomedical practice.
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