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培哚普利与氨氯地平对原发性高血压患者血压及与体液和电解质平衡相关激素相互作用的双盲交叉研究。

Double-blind crossover study of the interaction between perindopril and amlodipine on blood pressure and hormones related to fluid and electrolyte balance in patients with essential hypertension.

作者信息

Stokes G S, Monaghan J C, Berman K, Ryan M, Campbell D J

机构信息

Department of Clinical Pharmacology, Royal North Shore Hospital, St Leonards, NSW, Australia.

出版信息

J Hum Hypertens. 1998 Feb;12(2):129-34. doi: 10.1038/sj.jhh.1000557.

DOI:10.1038/sj.jhh.1000557
PMID:9504354
Abstract

This study was to investigate the interaction between low doses of perindopril (2 mg daily) and amlodipine (2.5 mg daily) on ambulatory blood pressure (BP), clinic BP, serum angiotensin-converting enzyme (ACE), plasma levels of renin (PRA), angiotensin II (Ang II), aldosterone, and atrial natriuretic peptide (alpha-h ANP) in subjects with essential hypertension. The study design was a parallel, two-period, placebo-controlled, double-blind crossover design, with 11 subjects receiving perindopril and 10 receiving amlodipine during the run-in phase. The addition of amlodipine to perindopril had no effect on ambulatory BP, whereas the addition of perindopril to amlodipine reduced both systolic (P = 0.027) and diastolic (P = 0.049) ambulatory BP. By contrast, the opposite result was obtained for clinic BP at trough, whereby the addition of amlodipine to perindopril reduced erect systolic BP (P = 0.036) and both supine and erect diastolic BP (P = 0.038) whereas the addition of perindopril to amlodipine was without effect. The addition of perindopril to amlodipine decreased serum ACE by 72% and increased PRA two-fold, without change in plasma levels of Ang II, aldosterone or alpha-h ANP. The addition of amlodipine to perindopril increased plasma aldosterone 1.7-fold but did not affect serum ACE, PRA, Ang II, or alpha-h ANP. These interactions between perindopril and amlodipine may have been conditioned by the specific effects of the therapy first given, as well as by the different circumstances of BP measurement (ambulatory vs clinic).

摘要

本研究旨在探讨低剂量培哚普利(每日2毫克)与氨氯地平(每日2.5毫克)对原发性高血压患者动态血压(BP)、诊室血压、血清血管紧张素转换酶(ACE)、血浆肾素水平(PRA)、血管紧张素II(Ang II)、醛固酮和心房利钠肽(α-h ANP)的相互作用。研究设计为平行、两阶段、安慰剂对照、双盲交叉设计,在导入期,11名受试者接受培哚普利,10名受试者接受氨氯地平。氨氯地平加至培哚普利对动态血压无影响,而培哚普利加至氨氯地平可降低收缩压(P = 0.027)和舒张压(P = 0.049)。相比之下,谷值时诊室血压得到相反结果,即氨氯地平加至培哚普利可降低直立位收缩压(P = 0.036)以及仰卧位和直立位舒张压(P = 0.038),而培哚普利加至氨氯地平则无作用。培哚普利加至氨氯地平可使血清ACE降低72%,使PRA增加两倍,而血浆Ang II、醛固酮或α-h ANP水平无变化。氨氯地平加至培哚普利可使血浆醛固酮增加至1.7倍,但不影响血清ACE、PRA、Ang II或α-h ANP。培哚普利与氨氯地平之间的这些相互作用可能受首次给予治疗的特定效应以及血压测量的不同情况(动态血压与诊室血压)影响。

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