The relationship between dose of methotrexate and incidence of liver fibrosis in patients with rheumatoid arthritis.

IF 1.4 Q3 RHEUMATOLOGY
Reumatologia Pub Date : 2025-02-01 Epub Date: 2025-02-23 DOI:10.5114/reum/199740
Mina AkbariRad, Zahra Rezaieyazdi, Ali Tajik, Banafshe Ataei, Mehrdad Sarabi, Hasan MehradMajd, Hasan Vossoughinia, Abdollah Firoozi
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引用次数: 0

Abstract

Introduction: Methotrexate (MTX) is a chemotherapy agent and immune system suppressant that can cause liver fibrosis in long-term usage. This study aimed to investigate the relationship between the dose of MTX and the incidence of liver fibrosis in patients with rheumatoid arthritis (RA).

Material and methods: This cohort study was conducted on RA patients with normal liver function who took MTX. Liver FibroScan and laboratory tests, including α2-macroglobulin, total bilirubin, g-glutamyltransferase, apolipoprotein A1, haptoglobin, and alanine transaminase was performed. The patients were divided into 2 groups regarding their cumulative dose of MTX and the rate of liver fibrosis incidence was compared between the 2 groups.

Results: In total, 60 RA patients with the mean age of 55.2 ±11.8 years were enrolled. The mean duration of MTX use in patients was 6.9 ±3.8 years, and it was higher in the higher cumulative dose MTX group (> 2 g) than in the lower cumulative dose group (< 2 g; p < 0.0001). The overall prevalence of grade 3 fibrosis was 3.33%. The prevalence of second- and third-degree liver fibrosis in patients receiving a lower cumulative dose was respectively 9 (28.1%) and 1 (3.1%), and in patients receiving a higher cumulative dose it was 7 (25%) and 1 (3.6%), respectively. There was no statistically significant difference between the 2 groups regarding the prevalence of liver fibrosis (p = 0.88). Both aspartate aminotransferase to platelet ratio index and Fibrosis Index Based on 4 Factors indices showed no significant difference between the 2 groups (p = 0.594, p = 0.232).

Conclusions: These results suggest that long-term treatment with a higher cumulative dose of MTX is not associated with a higher incidence of liver fibrosis in RA patients.

甲氨蝶呤剂量与类风湿关节炎患者肝纤维化发生率的关系。
简介:甲氨蝶呤(MTX)是一种化疗药物和免疫系统抑制剂,长期使用可引起肝纤维化。本研究旨在探讨MTX剂量与类风湿关节炎(RA)患者肝纤维化发生率之间的关系。材料与方法:本队列研究采用肝功能正常的RA患者服用甲氨蝶呤。肝纤维扫描和实验室检查,包括α2-巨球蛋白、总胆红素、g-谷氨酰转移酶、载脂蛋白A1、触珠蛋白和丙氨酸转氨酶。根据MTX累积剂量将患者分为两组,比较两组间肝纤维化发生率。结果:共纳入60例RA患者,平均年龄55.2±11.8岁。患者使用MTX的平均持续时间为6.9±3.8年,高累积剂量MTX组(bbb20 g)高于低累积剂量组(< 2 g;P < 0.0001)。3级纤维化的总患病率为3.33%。在接受较低累积剂量的患者中,二度和三度肝纤维化患病率分别为9(28.1%)和1(3.1%),而在接受较高累积剂量的患者中,二度和三度肝纤维化患病率分别为7(25%)和1(3.6%)。两组间肝纤维化发生率比较,差异无统计学意义(p = 0.88)。两组间天门冬氨酸转氨酶与血小板比率指数及基于4因素指标的纤维化指数差异均无统计学意义(p = 0.594, p = 0.232)。结论:这些结果表明,长期使用较高累积剂量的MTX治疗与RA患者较高的肝纤维化发生率无关。
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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来源期刊
Reumatologia
Reumatologia Medicine-Rheumatology
CiteScore
2.70
自引率
0.00%
发文量
44
审稿时长
10 weeks
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