Greenberg Jeffrey D, Ostrer Harry
NYU Hospital for Joint Diseases, New York, NY 10003, USA.
Bull NYU Hosp Jt Dis. 2007;65(2):139-42.
Despite the demonstrated efficacy of three different classes of biologic response modifiers (BRMs) for the treatment of rheumatoid arthritis (RA), there are currently no clinical predictors or biomarkers that can rationally guide physicians in the selection of BRMs for individual patients. One promising area of translational research for patients with RA is the field of pharmacogenetics. In the absence of industry-sponsored pharmacogenetic studies of BRMs, longitudinal clinical registries may represent the most promising setting for identifying genetic biomarkers. This review focuses on published pharmacogenetic studies of TNF antagonists and discusses related methodologic issues for pharmacogenetic research using clinical registries.
尽管已证实三类不同的生物反应调节剂(BRM)对类风湿关节炎(RA)治疗有效,但目前尚无临床预测指标或生物标志物能够合理指导医生为个体患者选择BRM。对RA患者而言,药物遗传学领域是转化研究中一个很有前景的方向。在缺乏行业资助的BRM药物遗传学研究的情况下,纵向临床登记可能是识别基因生物标志物最有前景的途径。本综述聚焦于已发表的肿瘤坏死因子拮抗剂药物遗传学研究,并讨论使用临床登记进行药物遗传学研究的相关方法学问题。