Julià A, Fernandez-Nebro A, Blanco F, Ortiz A, Cañete J D, Maymó J, Alperi-López M, Fernández-Gutierrez B, Olivè A, Corominas H, Erra A, Acosta-Colman I, Alonso A, López-Lasanta M, Tortosa R, Tornero J, Marsal S
Rheumatology Research Group, Vall d'Hebron Hospital Research Institute, Barcelona, Spain.
UGC Reumatología, Instituto de Investigación Biomédica de Málaga (IBIMA), Hospital Regional Universitario de Málaga, Universidad de Málaga, Málaga, Spain.
Pharmacogenomics J. 2016 Apr;16(2):147-50. doi: 10.1038/tpj.2015.31. Epub 2015 Apr 21.
Anti-Tumor Necrosis Factor (anti-TNF) drugs are biologic agents commonly used to treat rheumatoid arthritis (RA). However, anti-TNFs are not effective in approximately one out of four treated patients. We conducted a Genome-Wide Association Study (GWAS) to identify the genetic variation associated with the response to anti-TNF therapy in RA. In the discovery stage, 372 RA patients treated with an anti-TNF agent (infliximab, adalimumab or etanercept) were analyzed and treatment response was defined at 12 weeks of therapy. We found a genome-wide significant association in the MED15 gene with the response to etanercept (P<1.5e-8). Using an independent cohort of 245 RA patients, we performed a replication study of the most significant GWAS associations. We replicated the association at the MED15 locus and found suggestive evidence of association in the previously associated MAFB locus. The results of this study suggest novel mechanisms associated with the response to anti-TNF therapies.
抗肿瘤坏死因子(抗TNF)药物是常用于治疗类风湿性关节炎(RA)的生物制剂。然而,在接受治疗的患者中,约四分之一的人对抗TNF药物无效。我们进行了一项全基因组关联研究(GWAS),以确定与RA患者抗TNF治疗反应相关的基因变异。在发现阶段,分析了372例接受抗TNF药物(英夫利昔单抗、阿达木单抗或依那西普)治疗的RA患者,并在治疗12周时确定治疗反应。我们发现MED15基因与依那西普反应存在全基因组显著关联(P<1.5e-8)。我们使用245例RA患者的独立队列,对最显著的GWAS关联进行了重复研究。我们在MED15基因座重复了该关联,并在先前相关的MAFB基因座发现了关联的提示性证据。这项研究的结果提示了与抗TNF治疗反应相关的新机制。