Chen Wei, Srinivasan Sathanur R, Bond M Gene, Tang Rong, Urbina Elaine M, Li Shengxu, Boerwinkle Eric, Berenson Gerald S
Tulane Center for Cardiovascular Health, Tulane University Health Sciences Center, New Orleans, Louisiana 70112, USA.
Am J Hypertens. 2004 Jul;17(7):553-9. doi: 10.1016/j.amjhyper.2004.02.021.
The endothelial nitric oxide synthase (eNOS) gene is known to influence the regulation of blood pressure (BP) levels. However, whether the eNOS gene locus influences arterial stiffness independently of BP is unknown. This study examines the independent effect of the eNOS gene polymorphism (G894T) on arterial stiffness in 118 African American and 285 white young adults, aged 25 to 37 years. Arterial stiffness was measured from M-mode ultrasounds of common carotid artery using Peterson's (Ep) and Young's (YEM) elastic modulus. African Americans displayed a lower frequency of the T allele than did whites (0.131 v 0.321, P <.001). The T allele was associated with lower systolic BP in African Americans (P =.04) but not in whites. African Americans showed significantly higher values of Ep (that is, increased stiffness) than did whites (49.9 kPa vs 45.5 kPa, P =.003), whereas no such difference in ethnicity was found for YEM, a measure of elasticity adjusted for relative wall thickness. After controlling for sex, age, body mass index, insulin, heart rate, and mean arterial pressure, the T allele was associated with significantly lower values of Ep (P =.037) and YEM (P =.068) in African Americans. Although the genotype effect on Ep and YEM was not significant in whites, trends were similar to those in African Americans. In the total sample, including ethnicity as an additional covariate, the G894T genotype was significantly associated with Ep (P =.046) and YEM (P =.035). These results suggest that the allelic variation (G894T) of the eNOS gene or a locus closely linked to it is associated with lower arterial wall stiffness, adjusting for BP levels, in young adults.
已知内皮型一氧化氮合酶(eNOS)基因会影响血压(BP)水平的调节。然而,eNOS基因位点是否独立于血压影响动脉僵硬度尚不清楚。本研究调查了eNOS基因多态性(G894T)对118名年龄在25至37岁的非裔美国青年人和285名白人青年动脉僵硬度的独立影响。使用彼得森弹性模量(Ep)和杨氏弹性模量(YEM)通过颈总动脉的M型超声测量动脉僵硬度。非裔美国人中T等位基因的频率低于白人(0.131对0.321,P<.001)。T等位基因与非裔美国人较低的收缩压相关(P=.04),但与白人无关。非裔美国人的Ep值(即僵硬度增加)显著高于白人(49.9 kPa对45.5 kPa,P=.003),而对于根据相对壁厚调整的弹性指标YEM,未发现种族差异。在控制性别、年龄、体重指数、胰岛素、心率和平均动脉压后,T等位基因与非裔美国人显著较低的Ep值(P=.037)和YEM值(P=.068)相关。虽然基因型对Ep和YEM的影响在白人中不显著,但趋势与非裔美国人相似。在总样本中,将种族作为额外协变量纳入后,G894T基因型与Ep(P=.046)和YEM(P=.035)显著相关。这些结果表明,在年轻人中,eNOS基因的等位基因变异(G894T)或与其紧密连锁的位点与较低的动脉壁僵硬度相关,且已对血压水平进行了校正。