Pojoga L, Gautier S, Blanc H, Guyene T T, Poirier O, Cambien F, Benetos A
INSERM U337, Broussais Hospital, Paris, France.
Am J Hypertens. 1998 Jul;11(7):856-60. doi: 10.1016/s0895-7061(98)00048-x.
The renin-angiotensin-aldosterone system plays an important role in large artery structure and blood pressure homeostasis. Among the genes coding for different components of this system, the aldosterone synthase (CYP11B2) gene could play an important role, but has been less investigated. We examined the role of two variations of the aldosterone synthase gene (CYP11B2), one located in the promoter of the gene, T-344C, the other in the 7th exon, the T4986C (Val/Ala), on plasma levels of renin and aldosterone, blood pressure, and arterial stiffness in subjects with essential hypertension. Subjects of European origin (n = 216) were examined during a 1-day hospitalization. Treatment, if any, was interrupted for at least 21 days before. Arterial stiffness was evaluated by measuring pulse wave velocity. Renin and aldosterone levels were evaluated by using a radioimmunoassay. The two polymorphisms were in complete linkage disequilibrium, as suggested by the presence of only three haplotypes in this population (T-344T4986, T-344C4986, and C-344T4986). The mean age and blood pressure values were similar in the different genotypes. Presence of the -344C allele was associated with elevated levels of plasma aldosterone: 90 +/- 8 pg/mL for TT (n = 67), 110 +/- 6 pg/mL for TC (n = 107), and 129 +/- 10 pg/mL for CC (n = 42) (test of codominant effect, P < .002 after adjustment for age and 24-h Na+ urine excretion). Pulse wave velocity was also increased in the -344C allele carriers: 11.3 +/- 0.4 m/sec, 12.7 +/- 0.3 m/sec, 12.0 +/- 0.5 m/sec in the TT, TC, and CC genotypes, respectively. No association was found between the T4986C polymorphism and the studied variables. In patients with essential hypertension, a variant on the promoter region of the aldosterone synthase gene is associated with significant differences in plasma aldosterone levels and arterial stiffness. These differences are not associated with variations in blood pressure levels.
肾素-血管紧张素-醛固酮系统在大动脉结构和血压稳态中发挥重要作用。在编码该系统不同组分的基因中,醛固酮合酶(CYP11B2)基因可能起重要作用,但此前研究较少。我们研究了醛固酮合酶基因(CYP11B2)的两个变异的作用,一个位于基因启动子区,即T-344C,另一个位于第7外显子,即T4986C(Val/Ala),对原发性高血压患者的肾素和醛固酮血浆水平、血压及动脉僵硬度的影响。对216名欧洲裔受试者进行了为期1天的住院检查。如有治疗,至少在检查前21天中断治疗。通过测量脉搏波速度评估动脉僵硬度。采用放射免疫分析法评估肾素和醛固酮水平。这两个多态性处于完全连锁不平衡状态,因为该人群中仅存在三种单倍型(T-344T4986、T-344C4986和C-344T4986)。不同基因型的平均年龄和血压值相似。-344C等位基因的存在与血浆醛固酮水平升高相关:TT型(n = 67)为90±8 pg/mL,TC型(n = 107)为110±6 pg/mL,CC型(n = 42)为129±10 pg/mL(共显性效应检验,经年龄和24小时尿钠排泄校正后,P < 0.002)。-344C等位基因携带者的脉搏波速度也升高:TT、TC和CC基因型的脉搏波速度分别为11.3±0.4 m/秒、12.7±0.3 m/秒和12.0±0.5 m/秒。未发现T4986C多态性与所研究变量之间存在关联。在原发性高血压患者中,醛固酮合酶基因启动子区的一个变异与血浆醛固酮水平和动脉僵硬度的显著差异相关。这些差异与血压水平的变化无关。