Review of existing evidence demonstrates that methotrexate does not cause liver fibrosis.

IF 2
Hira Imad Cheema, Dirk Haselow, Jonathan Ankin Dranoff
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引用次数: 4

Abstract

It has long been believed that methotrexate in therapeutic doses causes progressive liver injury resulting in advanced fibrosis and cirrhosis. Historically, this was a common indication for serial liver biopsy. However, new evidence suggests that methotrexate may not be a direct cause of liver injury; rather the injury and fibrosis attributed to methotrexate may be mediated by other mechanisms, specifically non-alcoholic fatty liver disease. The recent widespread use of non-invasive assessment of liver fibrosis has provided new evidence supporting this hypothesis. Thus, we conducted a meta-analysis and systematic review to determine whether methotrexate is indeed a direct cause of liver injury. For the meta-analysis portion, a comprehensive literature search was performed to identify manuscripts relevant to the topic. Of the 138 studies examined, 20 met our inclusion criteria. However, only 3 studies had sufficient homogeneity to allow aggregation. Thus, the remainder of the study was dedicated to a critical review of all studies relevant to the topic with particular attention to populations examined, risk factors, and assessment of injury and/or fibrosis. Meta-analysis did not show a statistically significant association between methotrexate dose and liver fibrosis. Individual studies reported fibrosis related to confounding factors such as diabetes, obesity, pre-existing chronic liver disease but not methotrexate exposure. In conclusion, existing evidence demonstrates that advanced liver fibrosis and cirrhosis previously attributed to methotrexate are in fact caused by metabolic liver disease or other chronic liver diseases, but not by methotrexate itself. This observation should direct the care of patients treated with long-term methotrexate.

对现有证据的回顾表明甲氨蝶呤不会引起肝纤维化。
长期以来,人们一直认为治疗剂量的甲氨蝶呤会导致进行性肝损伤,导致晚期纤维化和肝硬化。从历史上看,这是连续肝活检的常见适应症。然而,新的证据表明甲氨蝶呤可能不是肝损伤的直接原因;相反,甲氨蝶呤引起的损伤和纤维化可能由其他机制介导,特别是非酒精性脂肪性肝病。最近广泛使用的无创肝纤维化评估为支持这一假设提供了新的证据。因此,我们进行了荟萃分析和系统评价,以确定甲氨蝶呤是否确实是肝损伤的直接原因。对于meta分析部分,进行了全面的文献检索,以确定与该主题相关的手稿。在138项研究中,20项符合我们的纳入标准。然而,只有3项研究具有足够的同质性,可以进行汇总。因此,该研究的剩余部分致力于对所有与该主题相关的研究进行批判性回顾,特别关注被检查人群、危险因素以及损伤和/或纤维化的评估。荟萃分析未显示甲氨蝶呤剂量与肝纤维化之间有统计学意义的关联。个别研究报告纤维化与糖尿病、肥胖、既往慢性肝病等混杂因素有关,但与甲氨蝶呤暴露无关。总之,现有证据表明,先前归因于甲氨蝶呤的晚期肝纤维化和肝硬化实际上是由代谢性肝病或其他慢性肝病引起的,而不是由甲氨蝶呤本身引起的。这一观察结果应指导长期接受甲氨蝶呤治疗的患者的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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