Association of the HLA-DRB1 with Scleroderma in Chinese Population

نویسندگان

  • Dongyi He
  • Jiucun Wang
  • Lin Yi
  • Xinjian Guo
  • Shicheng Guo
  • Gang Guo
  • Wenzhen Tu
  • Wenyu Wu
  • Li Yang
  • Rong Xiao
  • Yuan Li
  • Haiyan Chu
  • Syeling Lai
  • Li Jin
  • Hejian Zou
  • John D. Reveille
  • Shervin Assassi
  • Maureen D. Mayes
  • Xiaodong Zhou
چکیده

Multiple alleles of the Human leukocyte antigen (HLA) DRB1 have been strongly associated with systemic sclerosis (SSc) and its clinical or serological subsets. However, the associations vary in different ethnic populations. To define SSc-risk and/or -protective alleles of HLA-DRB1 in Chinese population, we studied a Han Chinese cohort containing 585 patients with SSc and 458 gender-matched, unrelated controls. The HLA-DRB1 genotyping was performed with sequence-based typing method. Exact p-values were obtained (Fisher's test) from 2×2 tables of allele frequency and disease status. The major SSc-risk allele subtypes of HLA-DRB1 are the DRB1*15∶02 and *16∶02 in this Chinese cohort. Particularly, DRB1*15∶02 was most significantly associated with anti-centromere autoantibodies (ACA) positive, and DRB1*16∶02 with anti-topoisomerase I autoantibodies (ATA) positive patients. On the other hand, DRB1*01∶01 and *04∶06 were strong SSc-protective alleles in Chinese, especially in patients who were ACA positive and had diffuse cutaneous SSc (dcSSc), respectively. In addition, DRB1*11 and *07∶01 also showed significant association with SSc as a risk for and protection from SSc, respectively, and which is consistent with the studies of Spanish, US Caucasian and Hispanic populations. DRB1*15 was associated with ATA positive Chinese SSc that is consistent with Black South African and Korean SSc. These findings of HLA-DRB1 alleles in association with Chinese SSc provide the growing knowledge of genetics of SSc, and indicate that the genetic heterogeneity among ethnicities may significantly impact the complex trait of SSc.

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عنوان ژورنال:

دوره 9  شماره 

صفحات  -

تاریخ انتشار 2014