Bek S, Bojesen A B, Nielsen J V, Sode J, Bank S, Vogel U, Andersen V
Focused Research Unit for Molecular Diagnostic and Clinical Research, IRS-Center Sonderjylland, Laboratory Center, Hospital of Southern Jutland, Aabenraa, Denmark.
Research Unit for E-mental Health, Mental Health Services in the Region of Southern Odense, Odense, Denmark.
Pharmacogenomics J. 2017 Oct;17(5):403-411. doi: 10.1038/tpj.2017.26. Epub 2017 Jun 13.
Rheumatoid arthritis (RA) is a chronic inflammatory disease that affects ~1% of the Caucasian population. Over the last decades, the availability of biological drugs targeting the proinflammatory cytokine tumour necrosis factor α, anti-TNF drugs, has improved the treatment of patients with RA. However, one-third of the patients do not respond to the treatment. We wanted to evaluate the status of pharmacogenomics of anti-TNF treatment. We performed a PubMed literature search and all studies reporting original data on associations between genetic variants and anti-TNF treatment response in RA patients were included and results evaluated by meta-analysis. In total, 25 single nucleotide polymorphisms were found to be associated with anti-TNF treatment response in RA (19 from genome-wide association studies and 6 from the meta-analyses), and these map to genes involved in T cell function, NFκB and TNF signalling pathways (including CTCN5, TEC, PTPRC, FCGR2A, NFKBIB, FCGR2A, IRAK3). Explorative prediction analyses found that biomarkers for clinical treatment selection are not yet available.
类风湿性关节炎(RA)是一种慢性炎症性疾病,影响约1%的白种人。在过去几十年中,针对促炎细胞因子肿瘤坏死因子α的生物药物(抗TNF药物)的出现改善了RA患者的治疗。然而,三分之一的患者对治疗无反应。我们想评估抗TNF治疗的药物基因组学状况。我们进行了PubMed文献检索,纳入了所有报告RA患者基因变异与抗TNF治疗反应之间关联的原始数据的研究,并通过荟萃分析评估结果。总共发现25个单核苷酸多态性与RA患者的抗TNF治疗反应相关(19个来自全基因组关联研究,6个来自荟萃分析),这些多态性定位于参与T细胞功能、NFκB和TNF信号通路的基因(包括CTCN5、TEC、PTPRC、FCGR2A、NFKBIB、FCGR2A、IRAK3)。探索性预测分析发现,目前尚无用于临床治疗选择的生物标志物。