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HLA Ⅰ类和Ⅱ类等位基因与 1 型糖尿病的微血管并发症有关。

HLA class I and II alleles are associated with microvascular complications of type 1 diabetes.

机构信息

Department of Epidemiology, Columbia University, Mailman School of Public Health, New York, NY, USA.

出版信息

Hum Immunol. 2013 May;74(5):538-44. doi: 10.1016/j.humimm.2013.01.013. Epub 2013 Jan 29.

Abstract

Although HLA alleles are associated with type 1 diabetes, association with microvascular complications remains controversial. We tested HLA association with complications in multiplex type 1 diabetes families. Probands from 425 type 1 diabetes families from the Human Biological Data Interchange (HBDI) collection were analyzed. The frequencies of specific HLA alleles in patients with complications were compared with the frequencies in complications-free patients. The complications we examined were: retinopathy, neuropathy, and nephropathy. We used logistic regression models with covariates to estimate odds ratios. We found that the DRB103:01 allele is a protective factor for complications (OR=0.58; p=0.03), as is the DQA105:01-DQB102:01 haplotype found in linkage disequilibrium with DRB103:01 (OR=0.59; p=0.031). The DRB104:01 allele showed no evidence of association (OR=1.13; p=0.624), although DRB104:01 showed suggestive evidence when the carriers of the protective DRB103:01 were removed from the analysis. The class II DQA103:01-DQB103:02 haplotype was not associated with complications, but the class I allele B39:06 (OR=3.27; p=0.008) suggested a strong positive association with complications. Our results show that in type 1 diabetes patients, specific HLA alleles may be involved in susceptibility to, or protection from, microvascular complications.

摘要

尽管 HLA 等位基因与 1 型糖尿病有关,但与微血管并发症的关联仍存在争议。我们在多基因 1 型糖尿病家族中检测了 HLA 与并发症的关联。分析了来自人类生物数据交换(HBDI)收集的 425 个 1 型糖尿病家族的先证者。将有并发症的患者中特定 HLA 等位基因的频率与无并发症的患者进行比较。我们检查的并发症包括:视网膜病变、神经病变和肾病。我们使用带有协变量的逻辑回归模型来估计优势比。我们发现 DRB103:01 等位基因是并发症的保护因素(OR=0.58;p=0.03),与 DRB103:01 连锁不平衡的 DQA105:01-DQB102:01 单倍型也是如此(OR=0.59;p=0.031)。DRB104:01 等位基因没有关联的证据(OR=1.13;p=0.624),尽管在从分析中去除保护性 DRB103:01 的携带者后,DRB104:01 显示出提示性证据。II 类 DQA103:01-DQB103:02 单倍型与并发症无关,但 I 类等位基因 B39:06(OR=3.27;p=0.008)表明与并发症有很强的正相关。我们的结果表明,在 1 型糖尿病患者中,特定的 HLA 等位基因可能与微血管并发症的易感性或保护有关。

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