奈比洛尔,第三代受体阻滞剂:高血压的现代治疗。一项多中心观察性研究的结果。

J von Fallois, H D Faülhaber
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引用次数: 0

摘要

背景:奈比洛尔是一种新型β受体阻滞剂,具有高β 1选择性和通过内皮细胞释放一氧化氮(NO)来调节血管直接反应的能力。它的抗高血压作用在每日一次的剂量下发展。该研究的主要目的是确定奈比洛尔对合并或不合并疾病的高血压患者的耐受性和降压效果。方法和结果:观察性研究在1529个中心进行,对6376例高血压患者进行了为期6周的研究。65岁以上患者的初始日剂量为5mg或2.5 mg。在治疗过程中,收缩压从最初的173 mmHg (+/- 18 mmHg)下降到观察结束时的144 mmHg (+/- 14 mmHg),平均(+/- 1个标准差)下降29 mmHg (+/- 17 mmHg)。舒张压从最初的101 mmHg (+/- 9 mmHg)下降到观察结束时的85 mmHg (+/- 8 mmHg),平均下降了16 mmHg (+/- 10 mmHg) (p < 0.001)。62.2%的患者舒张压恢复正常(< 90 mmHg)。研究开始时的平均心率为84(+/- 12),而研究结束时的平均心率为73(+/- 8)次/分钟(降低:10.6 +/- 10.3次/分钟)。血压和心率的降低取决于基线值,也就是说,与适度升高的初始值相比,较高的血压和较高的心率最初显示出更大的降低(两个参数)。观察期内胆固醇、甘油三酯、血糖均显著降低(p < 0.001)。甘油三酯下降13%,胆固醇下降8%。糖尿病患者受益最多(甘油三酯降低18%,胆固醇降低9%);这里,葡萄糖浓度下降了16%。内科医师评价奈比洛尔的疗效为93%,耐受性为97%(非常好或良好)。结论:在这项大型多中心观察性研究中,奈比洛尔被证明是一种安全、无副作用的降压药。其有利的代谢特性必须被认为是积极的,特别是关于冠心病的可能发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Nebivolol, a third generation beta blocker: the modern treatment of hypertension. Results of a multicentric observational study].

Background: Nebivolol represents a new therapeutic class of beta blockers with high beta1 selectivity and the ability to modu late the direct vascular reactions through the liberation of nitric oxide (NO) by the endothelial cell. Its antihypertensive action develops at a once-daily dosage. The main aim of the study was to determine the tolerability and antihypertensive efficacy of nebivolol in hypertensives with or without concomitant diseases.

Methods and results: The observational study was carried out in 1529 centers on 6376 patients with hypertension over a period of 6 weeks. The initial daily dosage was 5 mg or 2.5 mg in patients older than 65. Under treatment, the systolic blood pressure decreased by a mean (+/- 1 standard deviation) of 29 mmHg (+/- 17 mmHg) from 173 mmHg (+/- 18 mmHg) initially, to 144 mmHg (+/- 14 mmHg) by the end of the observation period. The diastolic blood pressure decreased by a mean of 16 mmHg (+/- 10 mmHg) from 101 mmHg (+/- 9 mmHg) initially to 85 mmHg (+/- 8 mmHg) by the end of the observation period (p < 0.001). Normalization of the diastolic blood pressure (< 90 mmHg) was achieved in 62.2% of the patients. The mean heart rate at the start of the study was 84 (+/- 12) vs. 73 (+/- 8) beats per minute by the end of the study (reduction: 10.6 +/- 10.3 beats per minute). The decrease in blood pressure and heart rate depended on the baseline values, that is, higher blood pressure and higher heart rates initially showed a greater reduction (both parameters) in comparison with moderately elevated initial values. Cholesterol, triglycerides and blood sugar decreased significantly (p < 0.001) duringthe observation period. For triglycerides the decrease was 13%, for cholesterol 8%. Diabetics benefited most (reduction in triglycerides 18%, in cholesterol 9%); here, the glucose concentration decreased by 16%. Physician-assessment of the efficacy of nebivolol was 93%, tolerability 97% (very good or good).

Conclusion: In this large multicentric observational study, the substance nebivolol proved to be a safe, largely side effect-free antihypertensive. Its favorable metabolic properties must be considered positive, in particular with regard to the possible development of coronary heart disease.

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