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1型糖尿病中白细胞介素-18基因多态性分析及哈迪-温伯格平衡检验

Analysis of polymorphisms of the interleukin-18 gene in type 1 diabetes and Hardy-Weinberg equilibrium testing.

作者信息

Szeszko Jeffrey S, Howson Joanna M M, Cooper Jason D, Walker Neil M, Twells Rebecca C J, Stevens Helen E, Nutland Sarah L, Todd John A

机构信息

Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge, UK.

出版信息

Diabetes. 2006 Feb;55(2):559-62. doi: 10.2337/diabetes.55.02.06.db05-0826.

Abstract

Recently, the interleukin-18 cytokine gene (IL18) was reported to be associated with type 1 diabetes. In the present report, we calculated that the reported genotypes of the two 5' region/promoter single nucleotide polymorphisms (SNPs), -607 (C-->A) (rs1946518) and -137 (G-->C) (rs187238), were not in Hardy-Weinberg equilibrium (HWE). We therefore investigated the association of the -607 and -137 SNPs in a U.K. type 1 diabetic Caucasian case-control collection (1,560 case and 1,715 control subjects tested at -607 and 4,323 case and 4,610 control subjects tested at -137) as well as a type 1 diabetic Caucasian collection comprised of families of European ancestry (1,347 families tested at -137 and 1,356 families tested at -607). No evidence for association with type 1 diabetes was found, including for the -607 A/A and C/A genotypes. To evaluate whether common variation elsewhere in the gene was associated with disease susceptibility, we analyzed eight IL18 tag SNPs in a type 1 diabetic case-control collection (1,561 case and 1,721 control subjects). No evidence for association was obtained (P = 0.11). We conclude that common allelic variation in IL18 is unlikely to contribute substantially to type 1 diabetes susceptibility in the populations tested and recommend routine application of tests for HWE in population-based studies for genetic association.

摘要

最近,有报道称白细胞介素-18细胞因子基因(IL18)与1型糖尿病相关。在本报告中,我们计算得出,所报道的两个5'区域/启动子单核苷酸多态性(SNP),即-607(C→A)(rs1946518)和-137(G→C)(rs187238)的基因型不符合哈迪-温伯格平衡(HWE)。因此,我们在一个英国1型糖尿病白种人病例对照样本(-607位点检测了1560例病例和1715例对照,-137位点检测了4323例病例和4610例对照)以及一个由欧洲血统家族组成的1型糖尿病白种人样本(-137位点检测了1347个家族,-607位点检测了1356个家族)中研究了-607和-137 SNP的关联性。未发现与1型糖尿病相关的证据,包括-607 A/A和C/A基因型。为了评估该基因其他位置的常见变异是否与疾病易感性相关,我们在一个1型糖尿病病例对照样本(1561例病例和1721例对照)中分析了8个IL18标签SNP。未获得相关证据(P = 0.11)。我们得出结论,在所检测的人群中,IL18的常见等位基因变异不太可能对1型糖尿病易感性有显著贡献,并建议在基于人群的遗传关联研究中常规应用哈迪-温伯格平衡检验。

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