Department of Dermatology and Allergology, University of Szeged, Hungary.
MTA-SZTE Dermatological Research Group, University of Szeged, Hungary; Department of Medical Genetics, University of Szeged, Hungary.
Hum Immunol. 2014 Feb;75(2):159-62. doi: 10.1016/j.humimm.2013.11.006. Epub 2013 Nov 20.
The aim of this study was to examine the role of single nucleotide polymorphisms (SNPs) and haplotypes of the tumor necrosis factor ligand superfamily member 15 (TNFSF15) gene in Hungarians with psoriasis and psoriatic arthritis. A case-control study was performed, and five TNFSF15 SNPs (rs3810936, rs6478108, rs6478109, rs7848647, rs7869487) were genotyped in 319 patients with psoriasis, 105 of whom also have psoriatic arthritis, and in 200 healthy individuals. Three haplotypes (A, B, C) based on these five SNPs were also analyzed. Our findings suggest that the rs6478109 SNP may be a genetic risk factor in psoriasis (p=0.0046), while haplotype C may be protective (p=0.0250). These results suggest that certain variants of the TNFSF15 gene contribute to the pathogenesis of the immune-mediated, multifactorial skin disease psoriasis, and that this difference is more readily apparent when groups of patients with and without psoriatic arthritis are examined separately.
本研究旨在探讨肿瘤坏死因子配体超家族成员 15(TNFSF15)基因单核苷酸多态性(SNPs)和单倍型在匈牙利银屑病和银屑病关节炎患者中的作用。进行了病例对照研究,对 319 名银屑病患者(其中 105 名患有银屑病关节炎)和 200 名健康个体的 5 个 TNFSF15 SNPs(rs3810936、rs6478108、rs6478109、rs7848647、rs7869487)进行了基因分型。还分析了基于这五个 SNPs 的三个单倍型(A、B、C)。我们的研究结果表明,rs6478109 SNP 可能是银屑病的遗传风险因素(p=0.0046),而单倍型 C 可能具有保护作用(p=0.0250)。这些结果表明,TNFSF15 基因的某些变体有助于免疫介导的多因素皮肤病银屑病的发病机制,并且当分别检查有和没有银屑病关节炎的患者组时,这种差异更为明显。