Conen David, Glynn Robert J, Buring Julie E, Ridker Paul M, Zee Robert Y L
Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital, 900 Commonwealth Avenue East, Boston, MA 02215, USA.
J Hypertens. 2008 Sep;26(9):1780-6. doi: 10.1097/HJH.0b013e3283077eef.
The renin-angiotensin system and endothelial function have both been associated with hypertension. The aim of the present study was to assess the relationship of six previously characterized gene variants in the renin-angiotensin system and the NOS3 gene with blood pressure progression and incident hypertension.
We analyzed data from 18 436 Caucasian women who participated in a prospective cohort study and were free of hypertension at baseline. Six previously characterized single nucleotide polymorphisms (NOS3 rs1800779, NOS3 rs3918226, NOS3 rs1799983, ACE rs1799752, AGT rs699, and AGTR1 rs5186) were genotyped. Blood pressure progression at 48 months and incident hypertension during the entire follow-up according to the different genotypes and inferred haplotypes were assessed by logistic regression and Cox proportional hazards models, respectively.
At 48 months, 47.4% of the women had blood pressure progression. The odds ratios (95% confidence intervals) for blood pressure progression associated with NOS3 rs1800779, NOS3 rs3918226, NOS3 rs1799983, ACE rs1799752, AGT rs699, and AGTR1 rs5186 were 1.00 (0.96-1.05), 1.00 (0.92-1.09), 0.99 (0.94-1.04), 0.96 (0.92-1.01), 1.04 (0.99-1.08), and 1.03 (0.98-1.08), respectively. During 9.8 years of follow-up, 29.6% of women developed incident hypertension. The hazard ratios (95% confidence interval) for the six polymorphisms were 1.01 (0.97-1.06), 1.06 (0.99-1.14), 1.05 (1.01-1.09), 0.99 (0.95-1.02), 1.01 (0.97-1.05), and 0.99 (0.95-1.04). NOS3 haplotypes were not significantly associated with blood pressure progression (P = 0.91) or incident hypertension (P = 0.10).
Blood pressure progression and incident hypertension are not consistently associated with six well-characterized genetic polymorphisms of the renin-angiotensin system and the NOS3 gene in a large cohort of Caucasian women.
肾素-血管紧张素系统和内皮功能均与高血压有关。本研究的目的是评估肾素-血管紧张素系统和NOS3基因中六个先前已鉴定的基因变异与血压进展和高血压发病之间的关系。
我们分析了18436名参与前瞻性队列研究且基线时无高血压的白人女性的数据。对六个先前已鉴定的单核苷酸多态性(NOS3 rs1800779、NOS3 rs3918226、NOS3 rs1799983、ACE rs1799752、AGT rs699和AGTR1 rs5186)进行基因分型。分别通过逻辑回归和Cox比例风险模型评估根据不同基因型和推断单倍型在48个月时的血压进展情况以及整个随访期间的高血压发病情况。
在48个月时,47.4%的女性出现血压进展。与NOS3 rs1800779、NOS3 rs3918226、NOS3 rs1799983、ACE rs1799752、AGT rs699和AGTR1 rs5186相关的血压进展的优势比(95%置信区间)分别为1.00(0.96 - 1.05)、1.00(0.92 - 1.09)、0.99(0.94 - 1.04)、0.96(0.92 - 1.01)、1.04(0.99 - 1.08)和1.03(0.98 - 1.08)。在9.8年的随访期间,29.6%的女性发生了高血压。这六个多态性的风险比(95%置信区间)分别为1.01(0.97 - 1.06)、1.06(0.99 - 1.14)、1.05(1.01 - 1.09)、0.99(0.95 - 1.02)、1.01(0.97 - 1.05)和0.99(0.95 - 1.04)。NOS3单倍型与血压进展(P = 0.91)或高血压发病(P = 0.10)无显著相关性。
在一大群白人女性中,血压进展和高血压发病与肾素-血管紧张素系统和NOS3基因的六个特征明确的基因多态性之间没有一致的关联。