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自身免疫性疾病相关单核苷酸多态性等位基因频率的种族差异。

Ethnic differences in allele frequency of autoimmune-disease-associated SNPs.

作者信息

Mori Mikako, Yamada Ryo, Kobayashi Kyoko, Kawaida Reimi, Yamamoto Kazuhiko

机构信息

Laboratory for Rheumatic Diseases, SNP Research Center, The Institute of Physical and Chemical Research, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan.

出版信息

J Hum Genet. 2005;50(5):264-266. doi: 10.1007/s10038-005-0246-8. Epub 2005 May 10.

Abstract

Several multiple, large-scale, genetic studies on autoimmune-disease-associated SNPs have been reported recently: peptidylarginine deiminase type 4 (PADI4) in rheumatoid arthritis (RA); solute carrier family 22 members 4 and 5 (SLC22A4 and 5) in RA and Crohn's disease (CD); programmed cell death 1 (PDCD1) in systemic lupus erythematosus (SLE), type 1 diabetes mellitus (T1D), and RA; and protein tyrosine phosphatase nonreceptor type 22 (PTPN22) in T1D, RA, and SLE. Because these reports on association were not always evaluated in multiple ethnic groups and because ethnic difference in allele frequency of the variants has been also reported, we investigated allele frequencies of nine SNPs in four autoimmune-disease-associated loci in Caucasian, African-descent, and Japanese populations. Although SNPs in PADI4 had similar allele frequency among three groups [maximal difference 11%; (P >0.05)], the other three loci revealed statistically significant allele frequency differences (maximal difference 39% (P <0.00001), 13% (P <0.00001), and 8% (P <0.00001) in SLC22A4, PDCD1, and PTPN22, respectively). Of note, three SNPs in the three loci that had allele frequency more than 8% in the Caucasian population were either not polymorphic at all or extremely rare in the Japanese population. Our data suggest that ethnic variations of polymorphisms should be evaluated in detail, and differences should be incorporated into investigations of susceptibility variants for common diseases.

摘要

最近已有多项关于自身免疫性疾病相关单核苷酸多态性(SNP)的大规模基因研究报道:类风湿关节炎(RA)中的肽基精氨酸脱亚氨酶4型(PADI4);RA和克罗恩病(CD)中的溶质载体家族22成员4和5(SLC22A4和5);系统性红斑狼疮(SLE)、1型糖尿病(T1D)和RA中的程序性细胞死亡1(PDCD1);以及T1D、RA和SLE中的蛋白酪氨酸磷酸酶非受体22型(PTPN22)。由于这些关联报道并非总是在多个种族群体中进行评估,且也有关于这些变异等位基因频率存在种族差异的报道,因此我们调查了白种人、非洲裔和日本人群中四个自身免疫性疾病相关基因座上九个SNP的等位基因频率。尽管PADI4中的SNP在三组中的等位基因频率相似[最大差异为11%;(P>0.05)],但其他三个基因座显示出具有统计学意义的等位基因频率差异(SLC22A4、PDCD1和PTPN22中的最大差异分别为39%(P<0.00001)、13%(P<0.00001)和8%(P<0.00001))。值得注意的是,在白种人人群中等位基因频率超过8%的三个基因座中的三个SNP,在日本人群中要么完全没有多态性,要么极其罕见。我们的数据表明,应详细评估多态性的种族差异,并将这些差异纳入常见疾病易感性变异的研究中。

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