依泊沙坦对动脉高血压患者纤溶/止血变量的影响:与氯沙坦的比较研究。

T K Makris, G Stavroulakis, D P Papadopoulos, P Krespi, A Hatzizacharias, A Zilidis, C Tsoukala, V E Votteas
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引用次数: 0

摘要

原发性高血压常伴有凝血/纤溶系统异常,易发生促凝状态。本研究的目的是研究血管紧张素II型1受体拮抗剂依泊沙坦和氯沙坦对先前未经治疗的高血压患者血浆止血/纤溶和内皮功能标志物水平的比较疗效。共86例高血压患者接受eprosartan 600mg(45例)或losartan 100mg(41例)单药治疗。测定治疗前后6个月血浆纤溶酶原激活物抑制剂-1 (PAI-1)抗原、组织纤溶酶原激活物抑制剂(tPA)抗原、血栓调节蛋白(TM)、组织因子通路抑制剂(TFPI)抗原、纤维蛋白原水平。两组患者的年龄、性别分布、体重指数、血脂、收缩压和舒张压水平以及测量指标的基线值相似。治疗6个月后,接受依泊沙坦治疗的患者收缩压明显降低,而舒张压无差异。两种药物治疗均与PAI-1抗原、TM、纤维蛋白原血浆水平显著降低和tPA抗原升高相关。依泊沙坦组对上述各项参数的有利改变明显大于氯沙坦组,两种药物的血浆TFPI水平下降程度相似。总之,我们的研究结果表明,与氯沙坦相比,新的血管紧张素II型1受体阻滞剂eprosartan单药治疗6个月对止血/纤溶状态的改善更有利。
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Eprosartan effect on fibrinolytic/hemostatic variables in arterial hypertension: a comparative study to losartan.

Essential hypertension is often accompanied by abnormalities of the coagulation/fibrinolytic system predisposing to a procoagulant state. The aim of the present study was to examine the comparative efficacy of the angiotensin II type 1 receptor antagonists eprosartan and losartan on plasma levels of hemostatic/fibrinolytic and endothelial function markers in a cohort of previously untreated hypertensive patients. A total of 86 patients whose hypertension was controlled by monotherapy with eprosartan 600 mg (45 patients) or losartan 100 mg (41 patients) were studied. The plasma levels of plasminogen activator inhibitor-1 (PAI-1) antigen, tissue plasminogen activator inhibitor (tPA) antigen, thrombomodulin (TM), tissue factor pathway inhibitor (TFPI) antigen, and fibrinogen were determined before and after 6 months of therapy. Age, sex distribution, body mass index, lipid profile, systolic and diastolic blood pressure levels, and baseline values of the measured markers were similar in both groups. After 6 months of therapy, systolic blood pressure was significantly lower in patients treated with eprosartan, while no differences were observed with respect to diastolic blood pressure. Treatment with both drugs was associated with a significant decrease in PAI-1 antigen, TM, fibrinogen plasma levels and an increase in tPA antigen. The favorable modification of all the above parameters was significantly greater in the eprosartan than in the losartan group, while TFPI plasma levels were decreased to a similar extent with both drugs. In conclusion, the results of our study indicate that 6-month monotherapy with a new angiotensin II type 1 receptor blocker, eprosartan, is associated with a more favorable modification of hemostatic/fibrinolytic status than with losartan.

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