Leucine 7 to proline 7 polymorphism in the neuropeptide y gene is associated with retinopathy in Type 2 diabetes

被引:47
作者
Niskanen, L
Voutilainen-Kaunisto, R
Teräsvirta, M
Karvonen, MK
Valve, R
Pesonen, U
Laakso, M
Uusitupa, MIJ
Koulu, M
机构
[1] Univ Kuopio, Dept Med, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Clin Nutr, FIN-70211 Kuopio, Finland
[3] Univ Kuopio, Dept Ophthalmol, FIN-70211 Kuopio, Finland
[4] Univ Turku, Dept Pharmacol & Clin Pharmacol, Turku, Finland
关键词
NPY gene polymorphism; retinopathy; Type; 2; diabetes;
D O I
10.1055/s-2000-7748
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study we tested the hypothesis that the Leu7Pro7 polymorphism in prepro neuropeptide Y (NPY) gene could be a risk marker for the development of diabetic retinopathy and analyzed a well characterized cohort of patients with Type 2 diabetes followed-up for 10 years from the time of diagnosis. The frequency of Leu7/Pro7-polymorphism was 9.3% (8 out of 86). At baseline, the frequency of retinopathy in patients with the Leu7/Pro7-polymorphism was 25% (2 out of 8) and in those without it 6.4% (5 out of 78) (p=0.126). At IO-year the respective figures were 88% and 50% (p=0.040). The odds ratio for Leu7/Pro7-polymorphism in logistic regression analysis adjusted for age, gender and HbA1c was 8.97 (95% confidence intervals 1.09-98.0; p=0.049). Our finding based on elderly Finnish Type 2 diabetic subjects suggests that the Leu7Pro7-genotype in preproNPY gene is associated with the development of diabetic retinopathy.
引用
收藏
页码:235 / 236
页数:2
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