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血管紧张素转换酶和血管紧张素原基因多态性在口服避孕药所致高血压中呈非随机分布。

Angiotensin-converting enzyme and angiotensinogen gene polymorphisms are non-randomly distributed in oral contraceptive-induced hypertension.

作者信息

Mulatero P, Rabbia F, di Cella S M, Schiavone D, Plazzotta C, Pascoe L, Veglio F

机构信息

Department of Medicine and Experimental Oncology, San Vito Hospital, University of Torino, Italy. mailto:

出版信息

J Hypertens. 2001 Apr;19(4):713-9. doi: 10.1097/00004872-200104000-00008.

Abstract

OBJECTIVES AND METHODS

Oral contraceptives (OC) usage increases serum angiotensinogen levels to three to five times normal and about 5% of these women develop arterial hypertension. The genetic contribution to this susceptibility to OC-induced hypertension is poorly understood. We have analyzed the genotypes of 149 hypertensive and 101 normotensive women using oral contraceptives, for three genetic polymorphisms in genes of the renin-angiotensin system: an insertion/deletion (I/ D) in the angiotensin converting enzyme (ACE) gene, the T235M polymorphism of the angiotensinogen gene (AGT) and a point mutation in its promoter.

RESULTS

After cessation of oral contraception the mean arterial pressures of the hypertensive women were separable into two non-overlapping groups; 88 of the women remained hypertensive and 61 returned to normal blood pressure. Both groups of hypertensive women had a similarly higher frequency of hypertensive relatives than the normotensive women, but were otherwise similar. The 235T allele of AGT was significantly increased in frequency in the 61 oral contraceptive-inducible hypertensive women compared with the controls and the 88 women that remained hypertensive. The ACE I/D genotypes were similarly distributed within the three groups of women, but were distinctly non-random in the oral contraceptive-induced hypertensive women when they were also classified by AGT genotype.

CONCLUSION

This statistical interaction of genotype frequencies suggests that the genetic basis of susceptibility to OC-induced hypertension is complex.

摘要

目的与方法

口服避孕药(OC)的使用会使血清血管紧张素原水平升高至正常水平的三到五倍,约5%的此类女性会出现动脉高血压。对这种口服避孕药诱发高血压易感性的遗传因素了解甚少。我们分析了149名使用口服避孕药的高血压女性和101名血压正常女性的基因型,检测了肾素 - 血管紧张素系统基因中的三种基因多态性:血管紧张素转换酶(ACE)基因的插入/缺失(I/D)、血管紧张素原基因(AGT)的T235M多态性及其启动子中的一个点突变。

结果

停止口服避孕药后,高血压女性的平均动脉压可分为两个不重叠的组;88名女性仍为高血压,61名女性血压恢复正常。两组高血压女性的高血压亲属频率均高于血压正常女性,但在其他方面相似。与对照组及88名仍为高血压的女性相比,61名口服避孕药诱发的高血压女性中AGT的235T等位基因频率显著增加。ACE的I/D基因型在三组女性中的分布相似,但在口服避孕药诱发的高血压女性中,按AGT基因型分类时,其分布明显非随机。

结论

基因型频率的这种统计学相互作用表明,口服避孕药诱发高血压易感性的遗传基础是复杂的。

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