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HLA DPA1, DPB1 Alleles and Haplotypes Contribute to the Risk Associated With Type 1 Diabetes

机译:HLA DPA1,DPB1等位基因和单倍型导致与1型糖尿病相关的风险

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摘要

Objective-To determine the relative risk associated with DPA1 and DPB1 alleles and haplotypes in type 1 diabetes.rnResearch design and methods-The frequency of DPA1 and DPB1 alleles and haplotypes in type 1 diabetic patients was compared to the family based control frequency in 1,771 families directly and conditional on HLA (B)-DRBl-DQAl-DQBl linkage disequilibrium. A relative predispositional analysis (RPA) was performed in the presence or absence of the primary HLA DR-DQ associations and the contribution of DP haplotype to individual DR-DQ haplotype risks examined.rnResults-Eight DPA1 and thirty-eight DPB1 alleles forming seventy-four DPA1-DPB1 haplotypes were observed; nineteen DPB1 alleles were associated with multiple DPA1 alleles. Following both analyses, type 1 diabetes susceptibility was significantly associated with DPB1*0301 (DPA1*0103-DPB1*0301) and protection with DPB1*0402 (DPA1*0103-DPB1*0402) and DPA1*0103-DPB1*0101 but not DPA1*0201-DPB1*0101. In addition, DPB1* 0202 (DPA1*0103-DPB1*0202) and DPB1*0201 (DPA1*0103-DPB1*0201) were significantly associated with susceptibility in the presence of the high risk and protective DR-DQ haplotypes. Three associations (DPB1*0301, *0402, and *0202) remained statistically significant when only the extended HLA-A1-B8-DR3 haplotype was considered, suggesting that DPB1 alone may delineate the risk associated with this otherwise conserved haplotype.rnConclusions-HLA DP allelic and haplotypic diversity contributes significantly to the risk for type 1 diabetes; DPB1*0301 (DPA1*0103-DPB1*0301) is associated with susceptibility and DPB1*0402 (DPA1*0103-DPB1*0402) and DPA1*0103-DPB1*0101 with protection. Additional evidence is presented for the susceptibility association of DPB1*0202 (DPA1*0103-DPB1*0202) and for a contributory role of individual amino acids and DPA1 or a gene in linkage disequilibrium in DR3-DPB1*0101 positive haplotypes.
机译:目的-确定1型糖尿病患者与DPA1和DPB1等位基因及单倍型相关的相对风险。研究设计和方法-将1型糖尿病患者中DPA1和DPB1等位基因及单倍型的频率与基于家庭的1771个家庭的对照频率进行比较直接且以HLA(B)-DRB1-DQAl-DQB1连锁不平衡为条件。在存在或不存在主要HLA DR-DQ关联以及DP单倍型对个体DR-DQ单倍型风险的贡献的情况下,进行了相对易感性分析(RPA)。结果-8个DPA1和38个DPB1等位基因形成了70-观察到四种DPA1-DPB1单倍型; 19个DPB1等位基因与多个DPA1等位基因相关。经过这两项分析,1型糖尿病易感性与DPB1 * 0301(DPA1 * 0103-DPB1 * 0301)和DPB1 * 0402(DPA1 * 0103-DPB1 * 0402)和DPA1 * 0103-DPB1 * 0101显着相关,但与DPA1无关* 0201-DPB1 * 0101。此外,在存在高风险和保护性DR-DQ单倍型的情况下,DPB1 * 0202(DPA1 * 0103-DPB1 * 0202)和DPB1 * 0201(DPA1 * 0103-DPB1 * 0201)与易感性显着相关。当仅考虑扩展的HLA-A1-B8-DR3单倍型时,三个关联(DPB1 * 0301,* 0402和* 0202)在统计学上仍然显着,这表明单独使用DPB1可以描述与该保守单倍型相关的风险。 DP等位基因和单倍型多样性显着增加了1型糖尿病的风险。 DPB1 * 0301(DPA1 * 0103-DPB1 * 0301)与磁化率相关,而DPB1 * 0402(DPA1 * 0103-DPB1 * 0402)和DPA1 * 0103-DPB1 * 0101具有保护性。对于DPB1 * 0202(DPA1 * 0103-DPB1 * 0202)的易感性关联以及DR3-DPB1 * 0101阳性单倍型中单个氨基酸和DPA1或基因在连锁不平衡中的贡献,也提供了其他证据。

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  • 来源
    《Diabetes》 |2010年第8期|P.2055-2062|共8页
  • 作者单位

    Victorian Transplantation & Immunogenetics Service, Australian Red Cross Blood Service, Melbourne, Australia;

    rnDepartment of Twin Research, King's College London, London, UK;

    rnClinical Chemistry, University Hospital, Malmo, Sweden;

    rnChildren's Hospital Oakland Research Institute, Oakland, California;

    rnVictorian Transplantation & Immunogenetics Service, Australian Red Cross Blood Service, Melbourne, Australia;

    rnChildren's Hospital Oakland Research Institute, Oakland, California;

    rnClinical Chemistry, University Hospital, Malmo, Sweden;

    rnChildren's Hospital Oakland Research Institute, Oakland, California;

    rnVictorian Transplantation & Immunogenetics Service, Australian Red Cross Blood Service, Melbourne, Australia;

    rnRoche Molecular Systems, Alameda, California;

    rnPublic Health Sciences, Bioinformatics & Genetics Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia;

    rnChildren's Hospital Oakland Research Institute, Oakland, California Roche Molecular Systems, Alameda, California;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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