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首页> 外文期刊>Journal of human hypertension >Acute effects of renin-angiotensin system blockade on arterial function in hypertensive patients.
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Acute effects of renin-angiotensin system blockade on arterial function in hypertensive patients.

机译:肾素-血管紧张素系统阻滞对高血压患者动脉功能的急性作用。

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The acute effects of the renin-angiotensin system (RAS) blockers may be important in some clinical settings. To assess the acute impact of such drugs on arterial function, we studied the effects of captopril 25 mg, quinapril 20 mg and telmisartan 80 mg on 100 hypertensive patients, according to a randomized, double-blind, placebo-controlled study. Central (aortic) blood pressure (BP) and augmentation index (AIx, a measure of wave reflections), as well as flow-mediated dilatation (FMD) of the brachial artery and forearm blood flow (FBF) (measures of conduit and resistance artery endothelial function, respectively), were evaluated before and 2 h after oral drug administration. Compared to placebo, captopril and quinapril decreased central systolic (by 7.5 mm Hg, P<0.05 and by 12.3 mm Hg, P<0.001) and diastolic BP (by 4.9 mm Hg, P<0.01 and by 8.4 mm Hg, P<0.001), whereas telmisartan had no significant effect (P=NS). Additionally, AIx was reduced after quinapril (absolute decrease of 7.2%, P<0.01) and marginally after captopril (decrease of 4.7%, P=0.07). Only quinapril led to a beneficial change of FMD (absolute increase of 2.7%, P<0.001). No treatment was related to significant changes of peak hyperaemic or 3-min hyperaemic FBF. In adjusted analyses, all the favourable alterations induced by quinapril were independent of potential confounding haemodynamic factors. Our data show that acute RAS inhibition with quinapril (20 mg) may be more beneficial in terms of arterial function and central haemodynamics compared to captopril (25 mg) or telmisartan (80 mg). Further studies are needed to investigate whether these acute arterial effects of quinapril are clinically significant.
机译:肾素-血管紧张素系统(RAS)阻滞剂的急性作用在某些临床环境中可能很重要。为了评估此类药物对动脉功能的急性影响,根据一项随机,双盲,安慰剂对照研究,我们研究了卡托普利25 mg,奎那普利20 mg和替米沙坦80 mg对100例高血压患者的作用。中央(主动脉)血压(BP)和增强指数(AIx,波反射的度量),以及肱动脉和前臂血流(FBF)的血流介导的扩张(FMD)(导管和阻力动脉的度量分别在口服药物之前和之后2小时评估内皮功能。与安慰剂相比,卡托普利和奎那普利降低中心收缩期(降低7.5 mm Hg,P <0.05和降低12.3 mm Hg,P <0.001)和舒张压(降低4.9 mm Hg,P <0.01和8.4 mm Hg,P <0.001) ),而替米沙坦则无明显作用(P = NS)。此外,奎奴普利治疗后AIx降低(绝对降低7.2%,P <0.01),卡托普利治疗后AIx降低(降低4.7%,P = 0.07)。只有奎那普利导致FMD的有益变化(绝对增加2.7%,P <0.001)。没有治疗与峰值充血或3分钟充血FBF的显着变化有关。在调整后的分析中,奎纳普利引起的所有有利改变均与潜在的混杂血液动力学因素无关。我们的数据表明,与卡托普利(25 mg)或替米沙坦(80 mg)相比,奎纳普利(20 mg)的急性RAS抑制在动脉功能和中枢血流动力学方面可能更有益。需要进一步研究以调查奎纳普利的这些急性动脉效应是否在临床上具有重要意义。

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