Institute of Human Genetics, University of Bonn, Sigmund-Freud-Str. 25, D-53127, Bonn, Germany.
Br J Dermatol. 2010 Apr;162(4):866-9. doi: 10.1111/j.1365-2133.2009.09598.x. Epub 2009 Dec 17.
Alopecia areata (AA) is a common hair loss disorder with a complex mode of inheritance. Autoimmune mechanisms are presumed to be crucial aetiologically. It is plausible that a number of autoimmune disorders may share a common genetic background. This phenomenon has been demonstrated in previous studies, which have shown an overlap of susceptibility alleles between AA and other autoimmune disorders. Recent studies have shown that genetic variants on the TRAF1/C5 (tumor necrosis factor receptor-associated factor 1, complement component 5) locus confer susceptibility to rheumatoid arthritis (RA).
To examine the role of the TRAF1/C5 locus in the development of AA using a large sample of 1,195 patients with AA and 1280 controls.
We genotyped the two most significant single nucleotide polymorphisms (SNPs) (rs10818488, rs2416808) from a former RA candidate gene study. After having obtained evidence for association, we performed a fine-mapping study and genotyped the locus with an additional 27 SNPs.
While no significant result was obtained for the overall sample, rs2416808 showed significant associations in the analysis of the subgroups with severe AA and with a positive family history. The most significant P-value for rs2416808 was in familial cases (P = 0.004, P(corr) = 0.026). The fine mapping revealed significant associations for four additional SNPs in the analysis of subgroups, with rs2416808 remaining the most significant marker.
Our results point to the involvement of the TRAF1/C5 locus in the aetiology of familial and severe AA, and provide further support for a shared aetiology between AA and other autoimmune disorders.
斑秃(AA)是一种常见的脱发疾病,具有复杂的遗传模式。自身免疫机制被认为在发病机制中起关键作用。许多自身免疫性疾病可能具有共同的遗传背景,这种现象在以前的研究中已经得到证实,这些研究表明 AA 和其他自身免疫性疾病之间存在易感性等位基因的重叠。最近的研究表明,TRAF1/C5(肿瘤坏死因子受体相关因子 1,补体成分 5)基因座上的遗传变异与类风湿关节炎(RA)易感性相关。
使用 1195 例 AA 患者和 1280 例对照的大样本,研究 TRAF1/C5 基因座在 AA 发病机制中的作用。
我们对来自以前的 RA 候选基因研究的两个最显著的单核苷酸多态性(SNP)(rs10818488,rs2416808)进行了基因分型。在获得关联证据后,我们进行了精细定位研究,并对该基因座进行了另外 27 个 SNP 的基因分型。
虽然总体样本未获得显著结果,但 rs2416808 在严重 AA 和阳性家族史亚组分析中显示出显著相关性。rs2416808 在家族性病例中的最显著 P 值为 0.004(P(corr) = 0.026)。精细定位显示在亚组分析中,另外 4 个 SNP 存在显著相关性,rs2416808 仍然是最显著的标记。
我们的结果表明 TRAF1/C5 基因座参与了家族性和严重 AA 的发病机制,并进一步支持 AA 和其他自身免疫性疾病之间存在共同的发病机制。