The genetic variant of lactase persistence C(-13910)T as a risk factor for type I and II diabetes in the Finnish population

被引:14
作者
Enattah, NS
Forsblom, C
Rasinperä, H
Tuomi, T
Groop, PH
Järvelä, I
机构
[1] Univ Helsinki, Cent Hosp, Mol Genet Lab, HUCH Lab Diagnost, FIN-00290 Helsinki, Finland
[2] Univ Helsinki, Dept Med Genet, Helsinki, Finland
[3] Natl Publ Hlth Inst, Dept Mol Med, Helsinki, Finland
[4] Folkhalsan Res Ctr, Helsinki, Finland
[5] Univ Helsinki, Cent Hosp, Dept Med, Div Nephrol, Helsinki, Finland
[6] Univ Helsinki, Cent Hosp, Dept Med, Div Internal Med, Helsinki, Finland
基金
芬兰科学院;
关键词
lactase persistence; lactose malabsorption; single nucleotide polymorphism; diabetes;
D O I
10.1038/sj.ejcn.1601971
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Objective: Lactase persistence (LP), the ability to maintain a high lactase activity throughout life, has been suggested to be a possible risk factor for diabetes. Recently, a single nucleotide polymorphism C (-13910) T, residing 14 kb from the 5' end of the lactase (LCT) gene was shown to be associated with LP. Here we have studied the relationship between C (13910) T polymorphism and diabetes in the Finnish population. Patients and design: In all, 1455 patients with type I and 615 with type II diabetes and 446 nondiabetic controls in the Finnish population were genotyped for the C (-13910) T polymorphism by PCR minisequencing. Results: No differences were detected in the LP genotype frequencies (CT&TT) between diabetic and nondiabetic subjects. Conclusions: We conclude that the C (-13910) T polymorphism associated with lifelong LP is not a risk factor for type I or type II diabetes in the Finnish population.
引用
收藏
页码:1319 / 1322
页数:4
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