
HLA–DPB1 and DPB2 are genetic loci for systemic sclerosis: A genome‐wide association study in Koreans with replication in North Americans
Author(s) -
Zhou Xiaodong,
Lee Jong Eun,
Arnett Frank C.,
Xiong Momiao,
Park Min Young,
Yoo Yeon Kyeong,
Shin Eun Soon,
Reveille John D.,
Mayes Maureen D.,
Kim Jin Hyun,
Song Ran,
Choi Ji Yong,
Park Ji Ah,
Lee Yun Jong,
Lee Eun Young,
Song Yeong Wook,
Lee Eun Bong
Publication year - 2009
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.24982
Subject(s) - single nucleotide polymorphism , genome wide association study , genetics , biology , snp , genetic association , autoantibody , human leukocyte antigen , population , immunology , medicine , gene , genotype , antigen , antibody , environmental health
Objective To identify systemic sclerosis (SSc) susceptibility loci via a genome‐wide association study. Methods A genome‐wide association study was performed in 137 patients with SSc and 564 controls from Korea using the Affymetrix Human SNP Array 5.0. After fine‐mapping studies, the results were replicated in 1,107 SSc patients and 2,747 controls from a US Caucasian population. Results The single‐nucleotide polymorphisms (SNPs) (rs3128930, rs7763822, rs7764491, rs3117230, and rs3128965) of HLA–DPB1 and DPB2 on chromosome 6 formed a distinctive peak with log P values for association with SSc susceptibility ( P = 8.16 × 10 −13 ). Subtyping analysis of HLA–DPB1 showed that DPB1*1301 ( P = 7.61 × 10 −8 ) and DPB1*0901 ( P = 2.55 × 10 −5 ) were the subtypes most susceptible to SSc in Korean subjects. In US Caucasians, 2 pairs of SNPs, rs7763822/rs7764491 and rs3117230/rs3128965, showed strong association with SSc patients who had either circulating anti–DNA topoisomerase I ( P = 7.58 × 10 −17 /4.84 × 10 −16 ) or anticentromere autoantibodies ( P = 1.12 × 10 −3 /3.2 × 10 −5 ), respectively. Conclusion The results of our genome‐wide association study in Korean subjects indicate that the region of HLA–DPB1 and DPB2 contains the loci most susceptible to SSc in a Korean population. The confirmatory studies in US Caucasians indicate that specific SNPs of HLA–DPB1 and/or DPB2 are strongly associated with US Caucasian patients with SSc who are positive for anti–DNA topoisomerase I or anticentromere autoantibodies.