Identification of independent risk loci for Graves disease within the MHC in the Japanese population

Kazuhiko Nakabayashi, Atsushi Tajima, Ken Yamamoto, Atsushi Takahashi, Kenichiro Hata, Yasuo Takashima, Midori Koyanagi, Hirofumi Nakaoka, Takashi Akamizu, Naofumi Ishikawa, Sumihisa Kubota, Shiro Maeda, Tatsuhiko Tsunoda, Michiaki Kubo, Naoyuki Kamatani, Yusuke Nakamura, Takehiko Sasazuki, Senji Shirasawa

研究成果: Article査読

14 被引用数 (Scopus)

抄録

To identify genetic variants that confer the risk of Graves disease (GD) in the Japanese population, we conducted a two-stage genome-wide association study (GWAS) using 1119 Japanese individuals with GD and 2718 unrelated controls, and a subsequent replication study using independent 432 GD cases and 1157 controls. We identified 34 single nucleotide polymorphisms (SNPs) to be significantly associated with GD in the GWAS phase. Twenty-two out of 34 SNPs remained positive in the replication study. All 22 SNPs were located within the major histocompatibility complex (MHC) locus on chromosome 6p21. No strong long-range linkage disequilibrium (LD) was observed among the 22 SNPs, indicating independent involvement of multiple loci within the MHC with the risk of GD. Multivariate stepwise logistic regression analysis selected rs3893464, rs4313034, rs3132613, rs4248154, rs2273017, rs9394159 and rs4713693, as markers for independent risk loci for GD. The analysis of LD between these seven SNPs and tagging SNPs for GD-associated human leukocyte antigen (HLA) alleles in the Japanese population (HLA-DPB1 0501 and HLA-A 0206) demonstrated that all of and five of seven SNPs were not in strong LD with HLA-DPB1 0501 and HLA-A 0206, respectively. Although causal variants remain to be identified, our results demonstrate the existence of multiple GD susceptibility loci within the MHC region.

本文言語English
ページ(範囲)772-778
ページ数7
ジャーナルJournal of Human Genetics
56
11
DOI
出版ステータスPublished - 11-2011

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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