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载脂蛋白D基因多态性:瑙鲁和印度南部2型糖尿病患者的一种新遗传标记

Apolipoprotein D gene polymorphism: a new genetic marker for type 2 diabetic subjects in Nauru and south India.

作者信息

Baker W A, Hitman G A, Hawrami K, McCarthy M I, Riikonen A, Tuomilehto-Wolf E, Nissinen A, Tuomilehto J, Mohan V, Viswanathan M

机构信息

Division of Clinical Sciences, John Curtin School of Medical Research, Canberra, Australia.

出版信息

Diabet Med. 1994 Dec;11(10):947-52. doi: 10.1111/j.1464-5491.1994.tb00252.x.

DOI:10.1111/j.1464-5491.1994.tb00252.x
PMID:7895459
Abstract

Type 2 diabetes is characterized by abnormalities in both glucose and lipoprotein metabolism and genes involved in lipid metabolism are legitimate candidates for involvement in Type 2 diabetes. We have previously reported an association in Nauruans between a Taq 1 polymorphism of the apolipoprotein D gene (apo D) and Type 2 diabetes. In this study these findings were investigated further in the Nauruan population as well as two other ethnic groups. In South Indian subjects, there was a significant difference in genotype distribution of apo D genotypes between diabetic subjects (n = 110) and controls (n = 88; p = 0.004) which was similar to that previously found in the Nauruan subjects. No such association was seen in elderly Finnish subjects (diabetic n = 69; impaired glucose tolerance n = 26 and normal glucose tolerance n = 31). Linkage between the apo D polymorphism and diabetes in 12 Nauruan families was only excluded under a highly penetrant dominant model and was unlikely under other single gene models. Since the beta cell glucose transporter gene (Glut 2) is found in a similar chromosomal location to apo D, South Indian subjects (diabetic n = 95 and controls n = 56) were typed at this locus. No association between diabetes and the Glut 2 Taq I polymorphism was found in the South Indian subjects. Furthermore, there was no evidence of linkage disequilibrium between the apo D and Glut 2 genes. In conclusion, apo D might act as a modifying gene for Type 2 diabetes in some ethnic groups.

摘要

2型糖尿病的特征是葡萄糖和脂蛋白代谢均异常,参与脂质代谢的基因是2型糖尿病发病的合理候选基因。我们之前曾报道过,在瑙鲁人群中,载脂蛋白D基因(apo D)的Taq 1多态性与2型糖尿病之间存在关联。在本研究中,我们在瑙鲁人群以及另外两个种族群体中进一步研究了这些发现。在南印度受试者中,糖尿病患者(n = 110)和对照组(n = 88;p = 0.004)的apo D基因型分布存在显著差异,这与之前在瑙鲁受试者中发现的情况相似。在芬兰老年受试者中未发现此类关联(糖尿病患者n = 69;糖耐量受损者n = 26,糖耐量正常者n = 31)。仅在高度显性遗传模型下排除了12个瑙鲁家庭中apo D多态性与糖尿病之间的连锁关系,在其他单基因模型下不太可能存在连锁关系。由于β细胞葡萄糖转运蛋白基因(Glut 2)与apo D位于相似的染色体位置,因此对南印度受试者(糖尿病患者n = 95,对照组n = 56)进行了该位点的基因分型。在南印度受试者中未发现糖尿病与Glut 2 Taq I多态性之间存在关联。此外,没有证据表明apo D和Glut 2基因之间存在连锁不平衡。总之,apo D可能在某些种族群体中作为2型糖尿病的修饰基因发挥作用。

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