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Predictive genetic biomarkers for the efficacy of methotrexate in rheumatoid arthritis: a systematic review

机译:预测遗传生物标志物,用于甲氨蝶呤在类风湿性关节炎中的疗效:系统审查

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摘要

Multiple pharmacogenetic studies investigated the effectiveness of methotrexate. However, due to the use of nonvalidated outcomes, lack of validation or conflicting results it remains unclear if genetic markers can help to predict response to MTX treatment. Therefore, a systematic review was performed. PubMed was searched for articles reporting potential pharmacogenetic biomarkers associated (p < 0.05) with MTX efficacy using the validated endpoints DAS(28), EULAR, or ACR response criteria. The PICO method was used for study selection, and PRISMA guidelines to prepare the report. Thirty-five studies met the inclusion criteria, providing 39 potential genetic biomarkers in 19 genes. After Bonferroni correction, six genetic biomarkers were associated with the efficacy of MTX: ATIC rs7563206; SLC19A1 rs1051266; DHFR rs836788; TYMS rs2244500, rs2847153, and rs3786362 in at least one study. Only SLC19A1 rs1051266 was replicated in an independent cohort and promising for predicting methotrexate efficacy.
机译:多种药物发生研究研究了甲氨蝶呤的有效性。但是,由于使用非验证结果,如果遗传标记可以有助于预测对MTX治疗的反应,缺乏验证或矛盾的结果仍然不清楚。因此,进行了系统审查。搜查了Pubmed的文章报告了潜在的药物生物标志物(P <0.05),使用验证的终点DAS(28),欧洲或ACR响应标准进行MTX功效。 PICO方法用于学习选择,普遍指南准备报告。三十五项研究符合纳入标准,在19个基因中提供39个潜在的遗传生物标志物。在Bonferroni校正之后,六个遗传生物标志物与MTX的疗效相关:ATIC RS7563206; SLC19A1 rs1051266; DHFR RS836788; TYMS RS2244500,RS2847153和至少一项研究中的RS3786362。只有SLC19A1 RS1051266在独立的队列中被复制,并且有希望预测甲氨蝶呤疗效。

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