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糖尿病中的基因定位。遗传流行病学视角。

Mapping genes in diabetes. Genetic epidemiological perspective.

作者信息

Rich S S

机构信息

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis.

出版信息

Diabetes. 1990 Nov;39(11):1315-9. doi: 10.2337/diab.39.11.1315.

Abstract

Research on mapping diabetes-susceptibility genes is dependent on several factors, including the existence of a single major gene for susceptibility, genetic homogeneity, and the existence of appropriate clinical material. The power to detect susceptibility genes is dependent on the risks in relatives and the distance of genetic markers from the susceptibility genes. For insulin-dependent diabetes mellitus (IDDM), the best-fitting risk models are those with a single major locus with residual polygenic factors. The major locus effect is likely represented by genes in the HLA complex, because specific genotypes have been found to affect IDDM risk significantly. Thus, mapping the remaining polygenic IDDM susceptibility factors--each of small effect--is a difficult and long task. For non-insulin-dependent diabetes mellitus (NIDDM), the likely risk models result in few genes with moderate effect. Models of NIDDM have significant residual polygenic variation remaining, reflecting the importance of multiple loci with small effect, environmental effects, or genetic heterogeneity; however, the prospects for mapping genes that provide at least moderate susceptibility for NIDDM now appear promising.

摘要

糖尿病易感性基因定位的研究取决于几个因素,包括是否存在单一的主要易感基因、基因同质性以及合适临床材料的存在。检测易感基因的能力取决于亲属中的风险以及遗传标记与易感基因的距离。对于胰岛素依赖型糖尿病(IDDM),最适合的风险模型是具有单一主要位点并伴有残余多基因因素的模型。主要位点效应可能由HLA复合体中的基因所代表,因为已发现特定基因型会显著影响IDDM风险。因此,定位其余的多基因IDDM易感因素——每个因素的效应都较小——是一项艰巨而漫长的任务。对于非胰岛素依赖型糖尿病(NIDDM),可能的风险模型导致只有少数具有中等效应的基因。NIDDM模型仍有显著的残余多基因变异,这反映了多个小效应位点、环境效应或基因异质性的重要性;然而,现在定位那些为NIDDM提供至少中等易感性的基因的前景似乎很乐观。

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