Suppr超能文献

IDDM1的遗传结构:主要组织相容性复合体中的两个独立区域与易感性或保护性相关。比利时糖尿病登记处。

Genetic structure of IDDM1: two separate regions in the major histocompatibility complex contribute to susceptibility or protection. Belgian Diabetes Registry.

作者信息

Hanifi Moghaddam P, de Knijf P, Roep B O, Van der Auwera B, Naipal A, Gorus F, Schuit F, Giphart M J

机构信息

Department of Immunohematology and Blood Bank, University Hospital, Leiden, The Netherlands.

出版信息

Diabetes. 1998 Feb;47(2):263-9.

PMID:9519723
Abstract

We analyzed 11 markers in the IDDM1 region in 120 IDDM patients and 83 healthy control subjects who were fully matched for the highest risk HLA-DQA10301-DQB1 0302/DQA10501-DQB10201 genotype. Our study provides strong evidence that two regions in the major histocompatibility complex contribute to IDDM susceptibility or protection. First, despite selection for highest IDDM-associated risk DQ genotypes, this region displays extensive linkage disequilibrium (LD) differences between IDDM patients and control subjects. A second critical region was mapped around the microsatellite locus D6S273 centromeric of TNF, and it is approximately 200 kb in size. LD analysis shows that "diabetogenic haplotypes" may have resulted from a recombination telomeric of D6S1014 in the region of D6S273 and TNFa. Haplotype analysis using HLA and microsatellite loci refines IDDM risk assessment in carriers of the HLA-DQ highest risk genotype.

摘要

我们对120例1型糖尿病患者和83名健康对照者的IDDM1区域中的11个标记物进行了分析,这些健康对照者与最高风险的HLA-DQA10301-DQB10302/DQA10501-DQB10201基因型完全匹配。我们的研究提供了强有力的证据,表明主要组织相容性复合体中的两个区域与1型糖尿病易感性或保护性有关。首先,尽管选择了与1型糖尿病相关风险最高的DQ基因型,但该区域在1型糖尿病患者和对照者之间显示出广泛的连锁不平衡(LD)差异。第二个关键区域定位在TNF着丝粒的微卫星位点D6S273周围,大小约为200 kb。LD分析表明,“致糖尿病单倍型”可能是由于D6S273和TNFα区域中D6S1014的端粒重组所致。使用HLA和微卫星位点的单倍型分析改进了HLA-DQ最高风险基因型携带者的1型糖尿病风险评估。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验