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8号染色体上存在新型1型糖尿病易感基因座的证据。

Evidence for a novel type 1 diabetes susceptibility locus on chromosome 8.

作者信息

Sale Michèle M, FitzGerald Liesel M, Charlesworth Jacinta C, Bowden Donald W, Rich Stephen S

机构信息

Menzies Centre for Population Health Research, University of Tasmania, Hobart, Australia.

出版信息

Diabetes. 2002 Dec;51 Suppl 3:S316-9. doi: 10.2337/diabetes.51.2007.s316.

Abstract

Type 1 diabetes results from a combination of genetic susceptibility and environmental exposures. Susceptibility loci other than HLA and the insulin gene remain to be identified to account for the degree of familial clustering observed in this disorder. Early genome-wide scans provided suggestive evidence of linkage on chromosome 8q, prompting detailed analysis of this region. A total of 20 microsatellite markers spanning an 88-cM region of 8q11-24 were genotyped in 24 type 1 diabetes pedigrees from Wisconsin that contained 39 affected sib-pairs. Multipoint linkage analyses provided close to suggestive evidence of linkage, with a multipoint logarithm of odds score (MLS) of 2.4 and Genehunter nonparametric logarithm of odds score (NPL) of 2.7 (P = 0.003). There is also evidence of linkage disequilibrium at peak marker D8S1823 for the 217bp allele (P = 0.037) using the pedigree disequilibrium test. Although our sample size was small, the multiple tests were consistent and our preliminary results suggested that 8q24 may harbor a novel population-specific type 1 diabetes susceptibility gene. Continued investigation of this region for a novel type 1 diabetes susceptibility gene appears justified.

摘要

1型糖尿病是由遗传易感性和环境暴露共同作用导致的。除了HLA和胰岛素基因外,其他易感基因座仍有待确定,以解释该疾病中观察到的家族聚集程度。早期的全基因组扫描提供了8号染色体q臂存在连锁的提示性证据,促使对该区域进行详细分析。在来自威斯康星州的24个1型糖尿病家系中,对跨越8q11 - 24区域88厘摩的20个微卫星标记进行了基因分型,这些家系包含39对患病同胞对。多点连锁分析提供了接近连锁的提示性证据,多点优势对数得分(MLS)为2.4,Genehunter非参数优势对数得分(NPL)为2.7(P = 0.003)。使用家系不平衡检验,在峰值标记D8S1823处,对于217bp等位基因也存在连锁不平衡的证据(P = 0.037)。尽管我们的样本量较小,但多次检验结果一致,我们的初步结果表明8q24可能含有一个新的人群特异性1型糖尿病易感基因。继续对该区域进行新型1型糖尿病易感基因的研究似乎是合理的。

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