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培哚普利、依那普利、氯沙坦和替米沙坦治疗超重或肥胖高血压患者的随机试验。

Randomized trial of perindopril, enalapril, losartan and telmisartan in overweight or obese patients with hypertension.

机构信息

Volgograd State Medical University, Volgograd, Russia.

出版信息

Clin Drug Investig. 2013 Aug;33(8):553-61. doi: 10.1007/s40261-013-0094-9.

Abstract

BACKGROUND AND OBJECTIVES

Obesity exacerbates hypertension and stimulates the renin-angiotensin-aldosterone system (RAAS). Full-dose RAAS inhibition could be a therapeutic option in overweight or obese patients with hypertension. This study compared four RAAS inhibitors at full therapeutic doses to determine their effect on blood pressure (BP) and cardiovascular risk factors in these patients.

METHODS

We conducted a 24-week, single-blind, randomized, parallel-group study in 120 overweight or obese patients (body mass index ≥27 kg/m(2)) with hypertension, aged 18-60 years. The primary endpoint was the change in mean 24-h systolic BP and diastolic BP from baseline to study end. Central BP, arterial stiffness, and metabolic and cardiac indices were also investigated. Patients were randomly allocated to perindopril 10 mg/day, enalapril 20 mg/day, losartan 100 mg/day or telmisartan 80 mg/day. Nonpharmacological interventions were also recommended.

RESULTS

Reductions in mean 24-h systolic BP (and diastolic BP) were all significant (p < 0.05 versus baseline) for perindopril, enalapril, losartan and telmisartan: systolic BP -22, -11, -12 and -15 mmHg, respectively; (and diastolic BP -13, -6, -13 and -12 mmHg, respectively). Aortic elasticity improved with perindopril and telmisartan. Perindopril was associated with the greatest reductions in central aortic BP and leptin levels [30 % versus 2 %, 7 % and 14 % with enalapril, losartan and telmisartan, respectively (all p < 0.05 versus perindopril)]. Reductions in other BP, echocardiographic, metabolic and anthropometric parameters occurred with all treatments.

CONCLUSION

Full-dose RAAS inhibition, particularly with perindopril, effectively reduces BP, improves arterial structure and regulates cardiovascular risk factors in overweight or obese patients with hypertension.

摘要

背景和目的

肥胖会加重高血压并刺激肾素-血管紧张素-醛固酮系统(RAAS)。在超重或肥胖的高血压患者中,全剂量 RAAS 抑制可能是一种治疗选择。本研究比较了四种全剂量 RAAS 抑制剂,以确定它们在这些患者中的血压(BP)和心血管危险因素方面的作用。

方法

我们进行了一项为期 24 周、单盲、随机、平行组研究,纳入了 120 名超重或肥胖(体重指数≥27kg/m2)的高血压患者,年龄在 18-60 岁之间。主要终点是从基线到研究结束时平均 24 小时收缩压和舒张压的变化。还研究了中心血压、动脉僵硬度以及代谢和心脏指数。患者被随机分配至培哚普利 10mg/天、依那普利 20mg/天、氯沙坦 100mg/天或替米沙坦 80mg/天。还推荐了非药物干预措施。

结果

培哚普利、依那普利、氯沙坦和替米沙坦均显著降低平均 24 小时收缩压(和舒张压)(与基线相比,均 p < 0.05):收缩压分别降低 22、11、12 和 15mmHg;(舒张压分别降低 13、6、13 和 12mmHg)。培哚普利和替米沙坦可改善主动脉弹性。与依那普利、氯沙坦和替米沙坦相比,培哚普利与中心主动脉血压和瘦素水平的最大降低相关[分别降低 30%、2%、7%和 14%(均 p < 0.05 与培哚普利相比)]。所有治疗均降低了其他 BP、超声心动图、代谢和人体测量参数。

结论

全剂量 RAAS 抑制,特别是使用培哚普利,可有效降低超重或肥胖的高血压患者的血压,改善动脉结构并调节心血管危险因素。

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