首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >A dose ranging study of atenolol in hypertension: fall in blood pressure and plasma renin activity beta-blockade and steady-state pharmacokinetics.
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A dose ranging study of atenolol in hypertension: fall in blood pressure and plasma renin activity beta-blockade and steady-state pharmacokinetics.

机译:阿替洛尔在高血压中的剂量范围研究:血压和血浆肾素活性下降β受体阻滞剂和稳态药代动力学。

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摘要

The relationship between the oral dosage and plasma concentration of the long-acting cardioselective beta-adrenoceptor blocker atenolol and the antihypertensive response to the the degree of beta-adrenoceptor blockade and change in plasma renin activity (PRA) was evaluated in patients with mild-to-moderate essential hypertension in a double-blind, randomized, between-patient, dose-ranging (25, 50 or 100 mg once daily for 4 weeks) study. The optimum, or minimum, daily dose of atenolol to treat patients with mild-to-moderate hypertension was not clearly identified in this study. A between-treatment comparison did not demonstrate that all blood pressure falls were always less in the 25 mg group than in the other two groups. Calculation of beta-error or the power for the negative results between doses suggested that a large sample size is required to draw a conclusion that no dose-antihypertensive relationship of atenolol exists in the treatment of mild-to-moderate hypertension. A relatively flat plasma concentration-antihypertensive response relationship was observed. Steady-state plasma concentrations of atenolol were dose-related and renal drug clearance was well correlated with individual creatinine clearance. beta-adrenoceptor blockade was better correlated with plasma atenolol concentration. Correlations which were less strong were between plasma drug concentration and change in various blood pressures and between blood pressure falls and beta-adrenoceptor blockade. There was no relationship between the fall in blood pressure and change in PRA. Atenolol appeared to suppress PRA in an all-or-none fashion.
机译:评估轻度至轻度患者的长效心脏选择性β-肾上腺素受体阻滞剂阿替洛尔的口服剂量与血浆浓度之间的关系以及对β-肾上腺素受体阻滞程度和血浆肾素活性(PRA)变化的降压反应中度原发性高血压在双盲,随机,患者之间,剂量范围内(每天25、50或100毫克,连续4周)。在这项研究中没有明确确定治疗轻度至中度高血压患者的最佳或最小剂量的阿替洛尔。治疗之间的比较未显示25 mg组的所有血压下降始终低于其他两组。 β-误差或剂量之间阴性结果的功效的计算表明,需要大量的样本才能得出结论,在轻度至中度高血压的治疗中不存在阿替洛尔的剂量-高血压关系。观察到相对平坦的血浆浓度-高血压反应关系。阿替洛尔的稳态血药浓度与剂量有关,肾药物清除率与个体肌酐清除率密切相关。 β-肾上腺素受体阻滞剂与血浆阿替洛尔浓度更好地相关。血浆药物浓度与各种血压变化之间以及血压下降与β-肾上腺素受体阻滞之间的相关性较弱。血压下降与PRA变化之间没有关系。阿替洛尔似乎以全有或全无的方式抑制PRA。

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