Conen D, Glynn R J, Buring J E, Ridker P M, Zee R Y
Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02215, USA.
J Intern Med. 2008 Apr;263(4):376-85. doi: 10.1111/j.1365-2796.2007.01894.x. Epub 2007 Dec 7.
The renin-angiotensin system and endothelial function have both been implicated in the pathogenesis of type 2 diabetes. The aim of this study was to assess the relationship between a set of well-characterized genetic variants of the renin-angiotensin system and the endothelial nitric oxide synthase (NOS3) gene and the incidence of type 2 diabetes.
Prospective cohort study.
Women's Health Study, United States.
A total of 24,309 Caucasian women free of diabetes at baseline.
Six previously characterized single nucleotide polymorphisms (NOS3 rs1800779, NOS3 rs3918226, NOS3 rs1799983, ACE rs1799752, AGT rs699 and AGTR rs5186) were genotyped. Cox proportional-hazards models were constructed to compare the incidence of type 2 diabetes according to the different genotypes.
During a median follow-up of 10.2 years (interquartile range 9.6-10.6 years), 999 women developed type 2 diabetes. The age-adjusted incidence rates across the six genotypes were very similar, and ranged from 3.7 to 4.8 cases/1000 person-years of follow-up. The multivariable adjusted hazard ratios (95% confidence intervals) for rs1800779, rs3918226, rs1799983, rs1799752, rs699, and rs5186 were 1.01 (0.92-1.10), 1.09 (0.93-1.27), 0.95 (0.86-1.05), 1.04 (0.95-1.14), 1.08 (0.98-1.18), 1.01 (0.91-1.11), confirming the lack of association between the genotypes and incident type 2 diabetes. Stratification by body mass index revealed essentially unchanged results. Finally, there was no association between NOS3-haplotypes and incident type 2 diabetes.
We did not find an association between six well-characterized genetic polymorphisms of the renin-angiotensin system or the NOS3 gene and the occurrence of type 2 diabetes.
肾素-血管紧张素系统和内皮功能均与2型糖尿病的发病机制有关。本研究旨在评估肾素-血管紧张素系统和内皮型一氧化氮合酶(NOS3)基因一组特征明确的基因变异与2型糖尿病发病率之间的关系。
前瞻性队列研究。
美国妇女健康研究。
共有24309名基线时无糖尿病的白人女性。
对6个先前已明确的单核苷酸多态性(NOS3 rs1800779、NOS3 rs3918226、NOS3 rs1799983、ACE rs1799752、AGT rs699和AGTR rs5186)进行基因分型。构建Cox比例风险模型,以比较不同基因型的2型糖尿病发病率。
在中位随访10.2年(四分位间距9.6 - 10.6年)期间,999名女性患2型糖尿病。六种基因型的年龄调整发病率非常相似,范围为每1000人年随访3.7至4.8例。rs1800779、rs3918226、rs1799983、rs1799752、rs699和rs5186的多变量调整风险比(95%置信区间)分别为1.01(0.92 - 1.10)、1.09(0.93 - 1.27)、0.95(0.86 - 1.05)、1.04(0.95 - 1.14)、1.08(0.98 - 1.18)、1.01(0.91 - 1.11),证实基因型与2型糖尿病发病之间缺乏关联。按体重指数分层显示结果基本不变。最后,NOS3单倍型与2型糖尿病发病之间无关联。
我们未发现肾素-血管紧张素系统或NOS3基因六个特征明确的基因多态性与2型糖尿病的发生之间存在关联。