创新链/学科链/研发链/产业链

新药研发前沿动态 / 医药领域趋势进展

传统合成改善病情抗风湿药的遗传药理学研究进展

Research Advances in the Pharmacogenetics of Conventional Synthetic Disease-Modifying Antirheumatic Drugs

  • 摘要: 近年来,风湿病学研究迅速发展,类风湿关节炎(RA)诊疗指南持续更新,药物治疗策略不断优化。基于《2018年中国类风湿关节炎诊疗指南》,结合《2015年美国风湿病学会(ACR)RA治疗指南》、《2016年欧洲风湿病防治联合会(EULAR)RA治疗指南》的治疗策略与用药建议,分析各指南推荐传统合成改善病情抗风湿药(csDMARDs)甲氨蝶呤、来氟米特、柳氮磺吡啶、羟氯喹的遗传药理学研究进展。相关药物遗传药理学研究主要集中于药物转运体、代谢酶、作用靶点等方面,研究结果可作为临床用药选择方面的参考依据,但尚需大样本多人群的临床试验验证。

     

    Abstract: In recent years, with the rapid development of rheumatology, guidelines for the diagnosis and treatment of rheumatoid arthritis(RA) and the drug treatment strategies have been updated constantly. Based on the 2018 Chinese guideline for the diagnosis and treatment of rheumatoid arthritis and combined with the 2015 ACR guideline and the 2016 EULAR guideline, this article analyzed the research advances in the pharmacogenetics of conventional synthetic disease-modifying antirheumatic drugs (csDMARDs), including methotrexate, leflunomide, sulfasalazine and hydroxychloroquine. The relevant studies had focused on the research of drug transporter, drug-metabolizing enzyme, and drug target. The results of the study can be used as a reference for clinical drug selection though verification from clinical trials in large populations is still needed.

     

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