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在患有血脂异常的高血压患者中,与阿替洛尔加普伐他汀相比,奈必洛尔加普伐他汀的联合用药具有更有益的代谢特征:一项初步研究。

The combination of nebivolol plus pravastatin is associated with a more beneficial metabolic profile compared to that of atenolol plus pravastatin in hypertensive patients with dyslipidemia: a pilot study.

作者信息

Rizos Evangelos, Bairaktari Eleni, Kostoula Angeliki, Hasiotis George, Achimastos Apostolos, Ganotakis Emanuel, Elisaf Moses, Mikhailidis D P

机构信息

Department of Internal Medicine, Medical School, University of Ioannina, Greece.

出版信息

J Cardiovasc Pharmacol Ther. 2003 Jun;8(2):127-34. doi: 10.1177/107424840300800206.

Abstract

Nebivolol, a selective beta1-lipophilic blocker, achieves blood pressure control by modulating nitric oxide release in addition to b-blockade. This dual mechanism of action could result in minimum interference with lipid metabolism compared to atenolol, a classic beta1-selective blocker. Hypertensive patients commonly exhibit lipid abnormalities and frequently require statins in combination with the anti-hypertensive therapy. We conducted this trial in order to clarify the effect on the metabolic profile of beta-blocker therapy with atenolol or nebivolol alone, or in conjunction with pravastatin. Thirty hypertensive hyperlipidemic men and women (total cholesterol >240 mg/dL [6.2 mmol/L], low-density lipoprotein cholesterol >190 mg/dL [4.9 mmol/L], triglycerides <500 mg/dL [5.6 mmol/L]) were separated in two groups. One group consisted of 15 subjects on atenolol therapy (50 mg daily), and the other group included 15 subjects on nebivolol therapy (5 mg daily). After 12 weeks of beta-blocker therapy, pravastatin (40 mg daily) was added in both groups for another 12 weeks. Atenolol significantly increased triglyceride levels by 19% (P=.05), while nebivolol showed a trend to increase high-density lipoprotein cholesterol by 8% (NS) and to decrease triglyceride levels by 5% (NS). Atenolol significantly increased lipoprotein(a) by 30% (P=.028). Fibrinogen levels were equally and not significantly decreased in both groups by 9% and 7%, respectively. Furthermore, atenolol and nebivolol decreased serum high-sensitivity C-reactive protein levels by 14% (P=.05) and 15% (P=.05), respectively. On the other hand, both atenolol and nebivolol showed a trend to increase homocysteine levels (NS) by 13% and 11%, respectively. Although uric acid levels remained the same, atenolol significantly increased the fractional excretion of uric acid by 33% (P=.03). Following nebivolol administration, glucose levels remained the same, while insulin levels were reduced by 10% and the HOMA index (fasting glucose levels multiplied by fasting insulin levels and divided by 22.5) was reduced by 20% (P=.05). There were no significant differences between the two patient groups in the measured parameters after the administration of beta-blockers, except for triglycerides (P<.05) and the HOMA index (P=.05). The addition of pravastatin to all patients (n=30) decreased total cholesterol by 21% (P<.001), low-density lipoprotein cholesterol by 28% (P<.001), apolipoprotein-B by 22% (P<.001), apolipoprotein-E by 15% (P=.014) and lipoprotein(a) levels by 12% (P=.023). Moreover, homocysteine levels and C-reactive protein were reduced by 17% (P=.05) and 43% (P=.05), respectively. We conclude that nebivolol seems to be a more appropriate therapy in hypertensive patients with hyperlipidemia and carbohydrate intolerance. Finally, the addition of pravastatin could further correct the well-established predictors of cardiovascular events.

摘要

奈必洛尔是一种选择性β1亲脂性阻滞剂,除β受体阻滞作用外,还可通过调节一氧化氮释放来控制血压。与经典的β1选择性阻滞剂阿替洛尔相比,这种双重作用机制对脂质代谢的干扰可能最小。高血压患者通常存在脂质异常,常需要他汀类药物与抗高血压治疗联合使用。我们进行这项试验是为了阐明单独使用阿替洛尔或奈必洛尔,或与普伐他汀联合使用的β受体阻滞剂治疗对代谢谱的影响。30名高血压高血脂男性和女性(总胆固醇>240mg/dL[6.2mmol/L],低密度脂蛋白胆固醇>190mg/dL[4.9mmol/L],甘油三酯<500mg/dL[5.6mmol/L])被分为两组。一组由15名接受阿替洛尔治疗(每日50mg)的受试者组成,另一组包括15名接受奈必洛尔治疗(每日5mg)的受试者。β受体阻滞剂治疗12周后,两组均加用普伐他汀(每日40mg),持续12周。阿替洛尔使甘油三酯水平显著升高19%(P=0.05),而奈必洛尔有使高密度脂蛋白胆固醇升高8%(无统计学意义)和使甘油三酯水平降低5%(无统计学意义)的趋势。阿替洛尔使脂蛋白(a)显著升高30%(P=0.028)。两组纤维蛋白原水平分别同等程度且无显著地降低了9%和7%。此外,阿替洛尔和奈必洛尔分别使血清高敏C反应蛋白水平降低14%(P=0.05)和15%(P=0.05)。另一方面,阿替洛尔和奈必洛尔均有使同型半胱氨酸水平分别升高13%和11%的趋势(无统计学意义)。虽然尿酸水平保持不变,但阿替洛尔使尿酸排泄分数显著升高33%(P=0.03)。服用奈必洛尔后,血糖水平保持不变,而胰岛素水平降低了10%,稳态模型评估指数(空腹血糖水平乘以空腹胰岛素水平再除以22.5)降低了20%(P=0.05)。在服用β受体阻滞剂后,除甘油三酯(P<0.05)和稳态模型评估指数(P=0.05)外,两组患者在测量参数上无显著差异。所有患者(n=30)加用普伐他汀后,总胆固醇降低21%(P<0.001),低密度脂蛋白胆固醇降低28%(P<0.001),载脂蛋白B降低22%(P<0.001),载脂蛋白E降低15%(P=0.014),脂蛋白(a)水平降低12%(P=0.023)。此外,同型半胱氨酸水平和C反应蛋白分别降低17%(P=0.05)和43%(P=0.05)。我们得出结论,对于患有高脂血症和碳水化合物不耐受的高血压患者,奈必洛尔似乎是一种更合适的治疗方法。最后,加用普伐他汀可进一步纠正已明确的心血管事件预测指标。

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