Fornage M, Amos C I, Kardia S, Sing C F, Turner S T, Boerwinkle E
Human Genetics Center, University of Texas at Houston Health Science Center, 77225, USA.
Circulation. 1998 May 12;97(18):1773-9. doi: 10.1161/01.cir.97.18.1773.
The renin-angiotensin system regulates blood pressure through its effects on vascular tone, renal hemodynamics, and renal sodium and fluid balance.
Using data from a large population-based sample of 1488 siblings having a mean age of 14.8 years and belonging to the youngest generation of 583 randomly ascertained three-generation pedigrees from Rochester, Minn, we carried out variance components-based linkage analyses to evaluate the contribution of variation in four renin-angiotensin system gene regions (angiotensinogen, renin, angiotensin I-converting enzyme, and angiotensin II receptor type 1) to interindividual variation in systolic, diastolic, and mean arterial pressure. We rejected the null hypothesis that allelic variation in the region of the angiotensin-converting enzyme (ACE) gene does not contribute to interindividual blood pressure variability. After conditioning on measured covariates, variation in this region accounted for 0%, 13% (P=0.04), and 16% (P=0.04) of the interindividual variance in systolic, diastolic, and mean arterial pressures, respectively. These estimates were even greater in a subset of subjects with a positive family history of hypertension (0%, 29% [P=0.005], and 32% [P<0.005], respectively). In sex-specific analyses, genetic variation in the region of the ACE gene significantly influenced interindividual blood pressure variation in males (37% for SBP [P=0.03], 38% for DBP [P=0.04], and 53% for MAP [P<0.005]) but not in females.
Although it is possible that variation in a gene near the ACE gene may explain the observed results, knowledge about the physiological involvement of ACE in blood pressure regulation supports the proposition that the ACE gene itself influences blood pressure variability in a sex-specific manner.
肾素 - 血管紧张素系统通过对血管张力、肾血流动力学以及肾钠和液体平衡的影响来调节血压。
利用来自明尼苏达州罗切斯特市583个随机确定的三代家系中最年轻一代的1488名平均年龄为14.8岁的同胞的大规模人群样本数据,我们进行了基于方差成分的连锁分析,以评估四个肾素 - 血管紧张素系统基因区域(血管紧张素原、肾素、血管紧张素I转换酶和血管紧张素II 1型受体)的变异对收缩压、舒张压和平均动脉压个体间变异的贡献。我们拒绝了血管紧张素转换酶(ACE)基因区域的等位基因变异对个体间血压变异性无贡献的零假设。在对测量的协变量进行校正后,该区域的变异分别占收缩压、舒张压和平均动脉压个体间变异的0%、13%(P = 0.04)和16%(P = 0.04)。在有高血压家族史阳性的受试者子集中,这些估计值甚至更高(分别为0%、29% [P = 0.005]和32% [P < 0.005])。在性别特异性分析中,ACE基因区域的遗传变异显著影响男性个体间的血压变异(收缩压为37% [P = 0.03],舒张压为38% [P = 0.04],平均动脉压为53% [P < 0.005]),但对女性无影响。
虽然ACE基因附近的一个基因的变异可能解释观察到的结果,但关于ACE在血压调节中的生理参与的知识支持这样的观点,即ACE基因本身以性别特异性方式影响血压变异性。