Lee Young Ho, Choi Sung Jae, Ji Jong Dae, Song Gwan Gyu
Division of Rheumatology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Pharmacogenomics. 2016 Aug;17(13):1465-77. doi: 10.2217/pgs.16.27. Epub 2016 Aug 4.
The aim of the current study was to investigate whether FCGR polymorphisms are associated with responsiveness to anti-TNF-α therapy in patients with spondyloarthropathy, psoriasis, and Crohn's disease.
MATERIALS & METHODS: We conducted a meta-analysis to evaluate the association between the functional FCGR3A F158V and FCGR2A R131H polymorphisms and responsiveness to TNF blockers.
The meta-analysis indicated that responsiveness to TNF blockers was associated with the FCGR3A V allele (odds ratio: 3.308; 95% CI: 1.053-10.39; p = 0.040) and the FCGR2A RR + RH genotype (odds ratio: 3.904; p = 0.027) in patients with a follow-up time of ≥6 months.
FCGR3A V and FCGR2A R allele carriers show better responsiveness to anti-TNF-α therapy in patients with follow-up times ≥6 months.
本研究旨在调查Fcγ受体(FCGR)基因多态性是否与脊柱关节病、银屑病和克罗恩病患者对抗肿瘤坏死因子-α(TNF-α)治疗的反应性相关。
我们进行了一项荟萃分析,以评估功能性FCGR3A F158V和FCGR2A R131H基因多态性与TNF阻滞剂反应性之间的关联。
荟萃分析表明,在随访时间≥6个月的患者中,TNF阻滞剂反应性与FCGR3A V等位基因(比值比:3.308;95%置信区间:1.053 - 10.39;p = 0.040)以及FCGR2A RR + RH基因型(比值比:3.904;p = 0.027)相关。
在随访时间≥6个月的患者中,FCGR3A V和FCGR2A R等位基因携带者对抗TNF-α治疗表现出更好的反应性。