Koutsompina Maria-Loukia, Pappa Maria, Sakellariou Stratigoula, Gialouri Chrysoula G, Fragoulis George E, Androutsakos Theodoros
Department of Pathophysiology, "Laiko" Hospital, School of Medicine, National and Kapodistrian University of Greece, Athens, Greece.
First Department of Internal Medicine, "Laiko" Hospital, School of Medicine, National and Kapodistrian University of Greece, Athens, Greece.
Mediterr J Rheumatol. 2021 Sep 7;32(3):264-272. doi: 10.31138/mjr.32.3.264. eCollection 2021 Sep.
Methotrexate is an anchor-drug for the treatment of inflammatory arthritides affecting peripheral joints, such as rheumatoid and psoriatic arthritis (PsA), but also for other immune-mediated diseases like psoriasis. Although it is generally a well-tolerated drug, adverse effects often occur. Reversible derangement of liver function test is the most common laboratory adverse event. However, in some cases, liver cirrhosis and/or fibrosis can occur. Besides, many of these diseases like PsA and psoriasis are closely linked with clinical conditions and risk factors that also contribute to liver damage/cirrhosis, such as increased body mass index, dyslipidaemia and diabetes mellitus (DM). It has been hypothesised that the aforementioned risk factors along with methotrexate usage can act synergistically, causing liver damage in these patients. Herein, we describe a PsA patient with DM who developed fatal liver cirrhosis after 10 years of treatment with MTX. We also review the literature about the liver toxicity of MTX in the context of PsA and psoriasis, describing concurring risk factors and histopathological findings. PubMed and Scopus were searched, without date limits. The keywords "methotrexate" AND "psoriatic arthritis" OR "psoriasis" AND "Liver damage" OR "liver fibrosis" OR "cirrhosis" were used. We found that although fibrosis/cirrhosis is present in about 10-25% of the patients, MTX can rarely cause liver damage itself. However, it can exert its effect when other factors, like increased alcohol consumption and obesity coexist. Prospective studies are needed, specifically examining the hepatotoxicity of MTX in individuals with immune-mediated diseases.
甲氨蝶呤是治疗影响外周关节的炎性关节炎(如类风湿性关节炎和银屑病关节炎(PsA))的一线药物,也用于治疗其他免疫介导的疾病,如银屑病。尽管它通常是一种耐受性良好的药物,但不良反应经常发生。肝功能检查的可逆性紊乱是最常见的实验室不良事件。然而,在某些情况下,可能会发生肝硬化和/或肝纤维化。此外,许多这些疾病,如PsA和银屑病,与临床状况和风险因素密切相关,这些因素也会导致肝损伤/肝硬化,如体重指数增加、血脂异常和糖尿病(DM)。据推测,上述风险因素与甲氨蝶呤的使用可能会协同作用,导致这些患者肝损伤。在此,我们描述了一名患有DM的PsA患者,在接受MTX治疗10年后发生了致命的肝硬化。我们还在PsA和银屑病的背景下回顾了关于MTX肝毒性的文献,描述了并发的风险因素和组织病理学发现。检索了PubMed和Scopus,无日期限制。使用了关键词“甲氨蝶呤”和“银屑病关节炎”或“银屑病”以及“肝损伤”或“肝纤维化”或“肝硬化”。我们发现,虽然约10-25%的患者存在纤维化/肝硬化,但MTX本身很少导致肝损伤。然而,当其他因素,如饮酒增加和肥胖同时存在时,它可能会发挥作用。需要进行前瞻性研究,专门检查MTX对免疫介导疾病患者的肝毒性。