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HLA Analysis and Disease for Multiple Sclerosis

机译:多发性硬化症的HLA分析和疾病

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Alleles for HLA-A, HLA-B, HLA-C, HLA-DQB1, HLA-DRB1, and HLA-DRB were typed across 820 age, gender, and race matched participants; 677 for whom have Multiple Sclerosis (MS) vs. 143 that do not. Observed alleles were coded and subject to significance testing with the goal to identify those alleles significantly associated with MS. Of the 368 unique alleles observed, eight were identified to be significantly associated with MS 100% of the time over 50 rounds of cross-validation testing; specifically HLA-DQB 1~*003, HLA-DQB1~*00301, HLA-DQB1~*00602, HLA-DRB 1~*0404, HLA-DRBP1501, HLA-DRB1~*1516/18, HLA-DRB3~*02, and HLA-DRB4~*01 were identified. Allele based classification modeling performed with each round of cross-validation testing provided for an overall classification success rate of 70%. Inspection of the alleles identified to be significantly associated with MS reveal nearly all to have been previously reported to be associated with MS; including four alleles reported to have association with disease severity.
机译:HLA-A,HLA-B,HLA-C,HLA-DQB1,HLA-DRB1和HLA-DRB等位基因在820年代,性别和种族匹配参与者中键入; 677年为谁具有多发性硬化(MS)与143。观察到的等位基因被编码,并考虑了目标,以识别与MS显着相关的那些等位基因。在观察到的368个独特的等位基因中,八个被识别出与50多轮交叉验证测试的100%的时间显着相关;特别是HLA-DQB 1〜* 003,HLA-DQB1〜* 00301,HLA-DQB1〜* 00602,HLA-DRB 1〜* 0404,HLA-DRBP1501,HLA-DRB1〜* 1516/18,HLA-DRB3〜* 02和识别出HLA-DRB4〜* 01。基于等位基因的分类建模,每轮交叉验证测试都为整体分类成功率为70%。检查确定与MS显着相关的等位基因几乎所有据报道都与MS相关联。包括据报道的四个等位基因与疾病严重程度有关。

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