Negative association between type 1 diabetes and HLA DQB1*0602-DQA1*0102 is attenuated with age at onset. Swedish Childhood Diabetes Study Group.

J Graham, I Kockum, C B Sanjeevi, M Landin-Olsson, L Nyström, G Sundkvist, H Arnqvist, G Blohmé, F Lithner, B Littorin, B Scherstén, L Wibell, J Ostman, A Lernmark, N Breslow, G Dahlquist
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Abstract

HLA-associated relative risks of type 1 (insulin-dependent) diabetes mellitus were analysed in population-based Swedish patients and controls aged 0-34 years. The age dependence of HLA-associated relative risks was assessed by likelihood ratio tests of regression parameters in separate logistic regression models for each HLA category. The analyses demonstrated an attenuation with increasing age at onset in the relative risk for the positively associated DQB1*0201-A1*0502/B1*0302-A1*0301 (DQ2/8) genotype (P = 0.02) and the negatively associated DQB1*0602-A1*0102 (DQ6.2) haplotype (P = 0.004). At birth, DQ6.2-positive individuals had an estimated relative risk of 0.03, but this increased to 1.1 at age 35 years. Relative risks for individuals with DQ genotype 8/8 or 8/X or DQ genotype 2/2 or 2/X, where X is any DQ haplotype other than 2, 8 or 6.2, were not significantly age-dependent. An exploratory analysis of DQ haplotypes other than 2, 8 and 6.2 suggested that the risk of type 1 diabetes increases with age for DQB1*0604-A1*0102 (DQ6.4) and that the peak risk for the negatively associated DQB1*0301-A1*0501 haplotype is at age 18 years. There was also weak evidence that the risk for DQB1*0303-A1*0301 (DQ9), which has a positive association in the Japanese population, may decrease with age. We speculate that HLA-DQ alleles have a significant effect on the rate of beta cell destruction, which is accelerated in DQ2/8-positive individuals and inhibited, but not completely blocked, in DQ6.2-positive individuals.

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1型糖尿病与HLA DQB1*0602-DQA1*0102的负相关随发病年龄的增加而减弱。瑞典儿童糖尿病研究小组。
分析了以人群为基础的瑞典0-34岁患者和对照组中hla相关的1型(胰岛素依赖型)糖尿病的相对风险。HLA相关相对风险的年龄依赖性通过回归参数的似然比检验对每个HLA类别进行单独的logistic回归模型。结果表明,DQB1*0201-A1*0502/B1*0302-A1*0301 (DQ2/8)基因型与DQB1*0602-A1*0102 (DQ6.2)单倍型与DQB1*0602-A1*0102 (DQ6.2)单倍型的相对危险度随发病年龄的增加而降低(P = 0.004)。出生时,dq6.2阳性个体的相对风险估计为0.03,但在35岁时增加到1.1。DQ基因型为8/8或8/X,或DQ基因型为2/2或2/X(其中X为除2,8或6.2以外的任何DQ单倍型)的个体的相对风险与年龄无关。对2、8、6.2以外的DQ单倍型的探索性分析表明,DQB1*0604-A1*0102 (DQ6.4)的1型糖尿病风险随着年龄的增长而增加,负相关的DQB1*0301-A1*0501单倍型的风险在18岁时达到峰值。也有微弱的证据表明,DQB1*0303-A1*0301 (DQ9)的风险可能随着年龄的增长而降低,而DQ9在日本人群中呈正相关。我们推测HLA-DQ等位基因对β细胞的破坏速度有显著影响,在dq2 /8阳性个体中,β细胞的破坏速度加快,在dq6.2阳性个体中,β细胞的破坏速度受到抑制,但没有完全阻断。
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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Nomenclature for factors of the HLA system, update December 2001. Nomenclature for factors of the HLA system, 2002. Nomenclature for factors of the HLA System, update July 2001. Mouse cytokine gene nucleotide sequence alignments, 2000. Part IV. DRB1 alleles in polymyalgia rheumatica and rheumatoid arthritis in southern France
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