Qiu Qi, Huang Jing, Lin Yang, Shu Xiaoming, Fan Huizheng, Tu Zhihua, Zhou Youwen, Xiao Cheng
Institute of Clinical Pharmacology, Beijing Anzhen Hospital, Capital Medical University Institute of Clinical Medicine, China-Japan Friendship Hospital Beijing University of Chinese Medicine Department of Rheumatology, China-Japan Friendship Hospital, Beijing Department of Gastroenterology, People's Hospital of Yichun, Jiangxi Yichun Department of Rheumatology, Yili Kazak Autonomous Prefecture Hospital of Traditional Chinese Medicine, Xinjiang Yining, China Department of Dermatology and Skin Science, University of British Columbia Molecular Medicine Lab and Chieng Genomics Center, Vancouver Coastal Health Research Institute, Vancouver, BC, Canada.
Medicine (Baltimore). 2017 Mar;96(11):e6337. doi: 10.1097/MD.0000000000006337.
Methotrexate (MTX) is widely used and considered a first-line disease modifying antirheumatic drug (DMARD) for the treatment of rheumatoid arthritis (RA). However, 10% to 30% of patients discontinue therapy within a year of starting the treatment, usually because of undesirable side effects. Many of the relevant genes have been investigated to estimate the association between gene polymorphisms and MTX toxicity in RA patients, although inconsistent results have been reported.
We searched EMBASE and PubMed in February 2016 for polymorphisms and pharmacogenomics study of the toxicity of MTX monotherapy in RA patients. The meta-analysis was stratified by whether genetic variants associated with MTX toxicity.
A total of 42 publications that included 28 genes with 88 gene SNPs associated with the transporters, enzymes, and metabolites of MTX or the progression of RA were included in the SR, and 31 studies were included in 7 meta-analyses. The meta-analysis showed a significant association between the toxicity of MTX and the RFC-1 80G > A (rs1051266) polymorphism in the European RA patients.
RFC-1 80G > A (rs1051266) polymorphism was associated with MTX toxicity, and larger and more stringent study designs may provide more accurate results for the effect of these SNPs on the MTX toxicity.
甲氨蝶呤(MTX)被广泛应用,被认为是治疗类风湿关节炎(RA)的一线改善病情抗风湿药(DMARD)。然而,10%至30%的患者在开始治疗的一年内停止治疗,通常是因为不良副作用。许多相关基因已被研究,以评估基因多态性与RA患者MTX毒性之间的关联,尽管报道的结果并不一致。
我们于2016年2月在EMBASE和PubMed上搜索了关于RA患者MTX单药治疗毒性的多态性和药物基因组学研究。荟萃分析根据与MTX毒性相关的基因变异进行分层。
系统性综述纳入了42篇出版物,其中包括28个基因的88个基因单核苷酸多态性(SNP),这些SNP与MTX的转运体、酶、代谢产物或RA的进展相关,7项荟萃分析纳入了31项研究。荟萃分析显示,在欧洲RA患者中,MTX毒性与RFC-1 80G > A(rs1051266)多态性之间存在显著关联。
RFC-1 80G > A(rs1051266)多态性与MTX毒性相关,更大规模和更严格的研究设计可能会为这些SNP对MTX毒性的影响提供更准确的结果。