DQA1*Arg52,DQB1*nonAsp57, and DRB1*04 genotypes in Chinese children with insulin-dependent diabetes mellitus.

F Y Huang, Y J Lee, F S Lo, C H Wang, S P Lin, C H Hsu, H A Kao, K W Tsan, J G Chang
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引用次数: 2

Abstract

Ethnic comparisons are extremely important and useful for studying the HLA component involved in insulin-dependent diabetes mellitus (IDDM) predisposition. To date there have been only a few reports on the association of HLA loci and IDDM in Chinese. We report here a study on DQA1*Arg52, DQB1*nonAsp57, and DRB1*04 in IDDM children and control adults among Han Chinese living in Taiwan. One hundred and fourteen unrelated children (62 boys) with IDDM were studied. Their ages at diagnosis were between 0.3 and 15.0 years (6.8 +/- 3.6 years). The control population consisted of 120 randomly selected normal adults. DQA1*Arg52(+/+), DQB1*nonAsp57(+/+), and DRB1*04(+/-) were associated with IDDM (RR = 11.50, 2.21, and 2.82; p = 1.11 x 10(-15), 2.84 x 10(-3), and 1.98 x 10(-4), respectively). DQA1*Arg52, DQB1*nonAsp57, and DRB1*04 conferred risks for IDDM (RR = 12.79, 7.11, and 2.83; pc = 8.22 x 10(-4), 5.35 x 10(-3), and 5.68 x 10(-4), respectively). Combinations of DQA1*Arg52 and DRB1*04 conferred the highest risk for IDDM (RR = 19.64, pc = 5.4 x 10(-5)). DQA1*Arg52 was associated with IDDM in subjects with DQB1*nonAsp57+ (RR = 14.87, pc = 2.41 x 10(-4)) and DQB1*nonAsp57 was also associated with IDDM in subjects with DQA1*Arg52+ (RR = 8.41, pc = 1.54 x 10(-3)), suggesting that DQA1*Arg52 and DQB1*nonAsp57 are interacting. This study demonstrates that DQA1*Arg52, DQB1*nonAsp57, and DRB1*04 confer susceptibility for IDDM to Chinese children. A combination of DQA1*Arg52 and DRB1*04 confers the highest risk and it is suggested that a susceptibility gene might be situated between DQA1*Arg52 and DRB1*04 or both are synergistic. There is an interaction between DQA1*Arg52 and DQB1*nonAsp57 and homozygosity for DQA1*Arg52/DQB1*nonAsp57, which encodes four susceptibility DQ heterodimers, confers a high risk.

胰岛素依赖型糖尿病患儿DQA1*Arg52、DQB1*nonAsp57、DRB1*04基因型的研究
种族比较对于研究与胰岛素依赖型糖尿病(IDDM)易感性相关的HLA成分非常重要和有用。迄今为止,关于中国人HLA位点与IDDM之间关系的报道很少。本文报道了台湾地区汉族IDDM儿童和对照成人DQA1*Arg52、DQB1*nonAsp57和DRB1*04基因的研究。对114名无血缘关系的IDDM患儿(62名男孩)进行了研究。诊断年龄在0.3 ~ 15.0岁之间(6.8±3.6岁)。对照人群由随机选择的120名正常成年人组成。DQA1*Arg52(+/+)、DQB1*nonAsp57(+/+)、DRB1*04(+/-)与IDDM相关(RR = 11.50、2.21、2.82;P = 1.11 × 10(-15), 2.84 × 10(-3), 1.98 × 10(-4)。dq1 *Arg52、DQB1*nonAsp57、DRB1*04会增加IDDM的风险(RR = 12.79、7.11、2.83;PC = 8.22 × 10(-4), 5.35 × 10(-3), 5.68 × 10(-4)。DQA1*Arg52和DRB1*04的组合使IDDM的风险最高(RR = 19.64, pc = 5.4 × 10(-5))。DQA1*Arg52与DQB1*nonAsp57+患者IDDM相关(RR = 14.87, pc = 2.41 × 10(-4)), DQB1*nonAsp57与DQA1*Arg52+患者IDDM相关(RR = 8.41, pc = 1.54 × 10(-3)),提示DQA1*Arg52与DQB1*nonAsp57存在交互作用。本研究表明,dq1 *Arg52、DQB1*nonAsp57和DRB1*04与中国儿童IDDM的易感性有关。DQA1*Arg52与DRB1*04的组合风险最高,提示DQA1*Arg52与DRB1*04之间可能存在易感基因,或两者具有协同作用。DQA1*Arg52与DQB1*nonAsp57之间存在相互作用,编码4种易感性DQ异源二聚体的DQA1*Arg52/DQB1*nonAsp57纯合性较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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