Department of Urology, Çanakkale Onsekiz Mart University Medical Faculty, Çanakkale/Turkey.
Urology. 2011 Jun;77(6):1439-43. doi: 10.1016/j.urology.2010.10.019. Epub 2011 Jan 22.
To investigate the effects of alpha receptor blockers used in the treatment of benign prostatic hyperplasia (BPH) on endothelial functions, coagulation parameters, and arterial blood pressure.
One-hundred fifteen patients admitted to the treatment protocol because of symptomatic BPH were included in this prospective study. Patients were given the following treatments: doxazosin 4 mg/d (n = 25), terazosin 5 mg/d (n = 26), alfuzosin 10 mg/d (n = 26), tamsulosin 0.4 mg/d (n = 21), and observation (n = 17). All cases were evaluated before treatment and in the 12th week of treatment, according to biochemical parameters, endothelial functions, and arterial blood pressure. Biochemical parameters were bleeding time, coagulation time, prothrombin time, activated partial thromboplastin time, total prostate-specific antigen (PSA), and free PSA. Endothelial functions were evaluated with ultrasonography of the brachial artery.
When coagulation tests were evaluated, there were significant increases in bleeding and coagulation times in the groups using doxazosin and terazosin. Doxazosin and terazosin lowered arterial blood pressure significantly compared with other treatments. With regard to effects on endothelial function, there were significant differences in flow-mediated dilation rates of the brachial artery at 60 and 90 seconds before and during treatment in the alfuzosin and terazosin groups.
Alpha receptor blockers can decrease the risk of cardiovascular complications by both reducing platelet aggregation and protecting endothelial functions in patients with prostatic hyperplasia. The only drug with a favorable effect in all 4 areas of interest, including BPH symptoms, blood pressure, platelet aggregation, and endothelial functions, was terazosin.
研究用于治疗良性前列腺增生症(BPH)的α受体阻滞剂对血管内皮功能、凝血参数和动脉血压的影响。
115 例因 BPH 症状而接受治疗方案的患者被纳入这项前瞻性研究。患者接受以下治疗:多沙唑嗪 4mg/d(n=25)、特拉唑嗪 5mg/d(n=26)、阿夫唑嗪 10mg/d(n=26)、坦索罗辛 0.4mg/d(n=21)和观察(n=17)。所有病例均在治疗前和治疗第 12 周进行生化参数、血管内皮功能和动脉血压评估。生化参数包括出血时间、凝血时间、凝血酶原时间、活化部分凝血活酶时间、总前列腺特异性抗原(PSA)和游离 PSA。血管内皮功能通过肱动脉超声评估。
当评估凝血试验时,使用多沙唑嗪和特拉唑嗪的组中出血时间和凝血时间显著增加。与其他治疗相比,多沙唑嗪和特拉唑嗪显著降低了动脉血压。就对内皮功能的影响而言,在阿夫唑嗪和特拉唑嗪组中,治疗前后 60 秒和 90 秒时肱动脉血流介导的扩张率存在显著差异。
α受体阻滞剂可通过减少血小板聚集和保护前列腺增生症患者的血管内皮功能,降低心血管并发症的风险。在 BPH 症状、血压、血小板聚集和内皮功能这 4 个方面均有良好效果的唯一药物是特拉唑嗪。