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现有证据表明,甲氨蝶呤不会导致肝纤维化。

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

机构信息

Baptist Health, Little Rock, Arkansas, USA.

VA Connecticut Healthcare System-West Haven Campus, West Haven, Connecticut, USA

出版信息

J Investig Med. 2022 Oct;70(7):1452-1460. doi: 10.1136/jim-2021-002206. Epub 2022 Aug 24.

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.

摘要

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,进而导致晚期纤维化和肝硬化。从历史上看,这是进行连续肝活检的常见指征。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,归因于甲氨蝶呤的损伤和纤维化可能是由其他机制介导的,特别是非酒精性脂肪性肝病。最近,非侵入性肝纤维化评估的广泛应用为这一假说提供了新的证据。因此,我们进行了一项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。在荟萃分析部分,我们进行了全面的文献检索,以确定与该主题相关的手稿。在检查的 138 项研究中,有 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,研究的其余部分专门用于对与该主题相关的所有研究进行批判性审查,特别关注检查的人群、风险因素以及损伤和/或纤维化的评估。荟萃分析并未显示甲氨蝶呤剂量与肝纤维化之间存在统计学显著关联。个别研究报告了与糖尿病、肥胖、先前存在的慢性肝病等混杂因素相关的纤维化,但与甲氨蝶呤暴露无关。总之,现有证据表明,以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。这一观察结果应该指导接受长期甲氨蝶呤治疗的患者的护理。

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