Analysis of HLA-B polymorphism in insulin dependent diabetes mellitus in Japanese.

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Author(s)

    • Shao Wenshuo
    • Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University
    • Kimura Akinori
    • Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University
    • Yasunami Michio
    • Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University
    • Takahashi Megumi
    • Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University
    • Shibata Hiroki
    • Department of Molecular Pathogenesis, Medical Research Institute, Tokyo Medical and Dental University
    • Sakata Toshiie
    • Department of Internal Medicine I, Oita Medical University School of Medicine
    • Ota Masao
    • Department of Legal Medicine, Shinshu University School of Medicine
    • Inoko Hidetoshi
    • Department of Genetic Information, Division of Molecular Life Science, Tokai University of Medicine,

Abstract

<p>Insulin dependent diabetes mellitus (IDDM) is a classical organ-specific autoimmune disease of the pancreatic beta cells. We have previously reported that HLA-B61, along with HLA-B54 and DRB I *0405, was associated with IDDM in a Japanese population, suggesting the presence of an HLA-B-1inked risk factor which is independent of HLA-DRIDQ alleles. Because HLA-B6 1 antigen is encoded by two major B40-related alleles, B*4002 and B*4006, in Japanese, we re-examined the association with the HLA-B polymorphisms, and analyzed the microsatellite loci flanking to the HLA-B Iocus. The results indicated that the frequencies of both B*4002 (21. 6% vs. 12. 2%, OR=1. 99, P=0. 023, 95% CI=1. 09-3. 63) and B*4006 (19. 4% vs. 10. 5%, OR=2. 06, P=0. 024, 95% CI= 1. 09-3. 88) were increased in the patients, and that two microsatellite markers, C 1_4_1 and C 1_2_5, showed strong associations with IDDM. In addition, haplotypic association studies suggested that the HLA-B itself, not the flanking regions linked to the microsatellite alleles, conferred the risk of IDDM.</p>

Journal

  • Major Histocompatibility Complex

    Major Histocompatibility Complex 9(3), 163-169, 2003

    Japanese Society for Histocompatibility and Immunogenetics

Cited by:  1

Codes

  • NII Article ID (NAID)
    130005509796
  • Text Lang
    ENG
  • Article Type
    Journal Article
  • ISSN
    2186-9995
  • Data Source
    CJPref  J-STAGE 
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