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血管紧张素原基因M235T多态性与降压治疗后管壁厚度的降低

Angiotensinogen gene M235T polymorphism and reduction in wall thickness in response to antihypertensive treatment.

作者信息

Bozec Erwan, Fassot Céline, Tropeano Anne-Isabelle, Boutouyrie Pierre, Jeunemaitre Xavier, Lacolley Patrick, Dabire Hubert, Laurent Stéphane

机构信息

Department of Pharmacology, INSERM EMI 0107, Hôpital Européen Georges Pompidou, 20 rue Leblanc, 75015 Paris, France.

出版信息

Clin Sci (Lond). 2003 Nov;105(5):637-44. doi: 10.1042/CS20030156.

Abstract

The angiotensinogen M235T polymorphism has been linked to hypertension and cardiovascular disease. Carotid intima-media thickness (IMT) is an early marker of atherosclerosis. The objectives of the present study were to determine in previously untreated essential hypertensive patients whether carotid IMT was associated with the M235T polymorphism, and to determine whether the M235T polymorphism could influence the reduction of carotid IMT by antihypertensive treatment. Common carotid artery IMT was determined with a high-definition echotracking system in 98 previously untreated hypertensive patients in a cross-sectional study. A subgroup of 56 patients was included in a randomized double-blind parallel group study comparing the effect of the angiotensin-converting-enzyme-inhibitor enalapril with that of the beta-blocker celiprolol during a 5 month period. In the cross-sectional study, a multivariate analysis showed that the M235T genotype was a significant independent determinant of carotid IMT, explaining 7% of the variance. Carotid IMT was higher in patients homozygous for the T allele than in MM patients. In the longitudinal study, the reduction in carotid IMT after antihypertensive treatment was significantly ( P <0.01) higher in patients carrying the TT genotype than in patients carrying the MM genotype, despite similar reductions in blood pressure and independently of drug type. In conclusion, these data suggest that the angiotensinogen TT genotype at position 235 is a genetic marker for early carotid atherosclerosis in a hypertensive population and its regression under antihypertensive treatment.

摘要

血管紧张素原M235T基因多态性与高血压及心血管疾病相关。颈动脉内膜中层厚度(IMT)是动脉粥样硬化的早期标志物。本研究的目的是确定在未经治疗的原发性高血压患者中,颈动脉IMT是否与M235T基因多态性相关,以及M235T基因多态性是否会影响降压治疗对颈动脉IMT的降低作用。在一项横断面研究中,使用高清回声跟踪系统对98例未经治疗的高血压患者的颈总动脉IMT进行了测定。56例患者被纳入一项随机双盲平行组研究,比较血管紧张素转换酶抑制剂依那普利与β受体阻滞剂塞利洛尔在5个月期间的效果。在横断面研究中,多变量分析显示M235T基因型是颈动脉IMT的一个显著独立决定因素,可解释7%的变异。T等位基因纯合子患者的颈动脉IMT高于MM患者。在纵向研究中,尽管血压降低程度相似且与药物类型无关,但携带TT基因型的患者在降压治疗后颈动脉IMT的降低幅度显著高于携带MM基因型的患者(P<0.01)。总之,这些数据表明,235位的血管紧张素原TT基因型是高血压人群早期颈动脉粥样硬化及其在降压治疗下的消退情况的一个遗传标志物。

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