Ji Xu, Qi Hua, Li Dong-Bao, Liu Rong-Kun, Zheng Yang, Chen Hai-Ling, Guo Jin-Cheng
Department of Cardiovascular, Xuanwu Hospital of Capital Medical University Beijing 100053, China.
Int J Clin Exp Med. 2015 Jan 15;8(1):1173-7. eCollection 2015.
Aldosterone synthase is a mitochondrial enzyme that catalyzes the conversion of 11-deoxycorticosterone to the potent mineralocorticoid aldosterone. The gene encoding aldosterone synthase, CYP11B2, is associated with essential hypertension. But if the genetic variations in aldosterone synthesis could influence the antihypertensive response to Valsartan is not clear. A Chinese sample of 502 persons (217 women) was studied, which was divided into the hypertensive group (EH) of 345 persons and the normotensive group (NB) of 157 persons. Subjects were genotyped through the use of the polymerase chain reaction for the diallelic polymorphisms in CYP11B2. 98 persons of the essential hypertension group received 4 weeks therapy with valsartan. Blood pressure, 24-hour ambulatory blood pressure, biochemical index were also determined. The frequency of CC+CT genotypes in hypertensive group was significantly higher than that in normotensive group (P<0.05), the frequency of C allele of gene CYP11B2 (-344T/C) in hypertensive group was significantly higher than that in normotensive group (P<0.01). The descending values of SBP (systolic blood pressure), DBP (diastolic blood pressure), MAP (mean arterial pressure), 24 h SBP (mean SBP of 24 hours), 24 h DBP (mean DBP of 24 hours), 24 h MAP (mean arterial pressure of 24 hours) of CC+CT genotype group were significantly higher than those of the TT genotype group (P<0.05). The aldosterone synthase CYP11B2 (-344T/C) gene polymorphism is associated with essential hypertension in Chinese. And the aldosterone synthase CYP11B2 (-344T/C) gene polymorphism may be the predictor of the antihypertensive response to Valsartan.
醛固酮合酶是一种线粒体酶,可催化11-脱氧皮质酮转化为强效盐皮质激素醛固酮。编码醛固酮合酶的基因CYP11B2与原发性高血压相关。但醛固酮合成中的基因变异是否会影响缬沙坦的降压反应尚不清楚。对502名中国人(217名女性)的样本进行了研究,将其分为345人的高血压组(EH)和157人的正常血压组(NB)。通过聚合酶链反应对CYP11B2中的双等位基因多态性进行基因分型。98名原发性高血压组患者接受了4周的缬沙坦治疗。还测定了血压、24小时动态血压、生化指标。高血压组CC + CT基因型的频率显著高于正常血压组(P < 0.05),高血压组基因CYP11B2(-344T/C)的C等位基因频率显著高于正常血压组(P < 0.01)。CC + CT基因型组的收缩压(SBP)、舒张压(DBP)、平均动脉压(MAP)、24小时SBP(24小时平均SBP)、24小时DBP(24小时平均DBP)、24小时MAP(24小时平均动脉压)的下降值显著高于TT基因型组(P < 0.05)。醛固酮合酶CYP11B2(-344T/C)基因多态性与中国人群的原发性高血压相关。并且醛固酮合酶CYP11B2(-344T/C)基因多态性可能是缬沙坦降压反应的预测指标。