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Effects of aliskiren on the fibrinolytic system in patients with coronary artery disease receiving angiotensin-converting enzyme inhibitor or angiotensin II type 1 receptor blocker

机译:阿利吉仑对接受血管紧张素转换酶抑制剂或血管紧张素II 1型受体阻滞剂的冠心病患者纤溶系统的影响

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摘要

Aliskiren is a novel blood pressure-lowering agent acting as an oral direct renin inhibitor. We evaluated the effects of aliskiren on the fibrinolytic system in patients with coronary artery disease who were receiving angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin II type 1 receptor blockers (ARBs). We studied 17 patients with coronary artery disease whose systolic blood pressure was more than 130 mmHg despite treatment with ACEIs or ARBs. Aliskiren (150 mg) was added to ACEIs or ARBs, and was continued for 6 weeks. Aliskiren significantly decreased systolic blood pressure (140 +/- 6-128 +/- 8 mmHg, P < 0.001) and plasma renin activity (1.8 +/- 2.3-0.6 +/- 0.9 ng/ml/h, P < 0.01) after 6 weeks. However, it did not affect plasminogen activator inhibitor-1 (28.8 +/- 14.5-30.6 +/- 13.6 ng/ml, P = 0.84), fibrinogen (305 +/- 72 vs 301 +/- 71 mg/dl, P = 0.33), or D-dimer (0.49 +/- 0.24-0.51 +/- 0.28 mu g/ml, P = 0.70) levels. Our data suggested that patients receiving ACEIs or ARBs would not be expected to have any changes in biomarkers of the fibrinolytic system with additional pharmacologic inhibition of the renin-angiotensin-aldosterone system.
机译:Aliskiren是一种新型的降血压药,可作为口服直接肾素抑制剂。我们评估了阿利吉仑对接受血管紧张素转换酶抑制剂(ACEIs)或血管紧张素II 1型受体阻滞剂(ARB)的冠心病患者的纤溶系统的影响。我们研究了17例冠心病患者,尽管使用ACEI或ARB进行治疗,其收缩压仍超过130 mmHg。将阿利吉仑(150毫克)添加到ACEIs或ARB中,并持续6周。阿利吉仑显着降低收缩压(140 +/- 6-128 +/- 8 mmHg,P <0.001)和血浆肾素活性(1.8 +/- 2.3-0.6 +/- 0.9 ng / ml / h,P <0.01) 6周后。但是,它不会影响纤溶酶原激活物抑制剂-1(28.8 +/- 14.5-30.6 +/- 13.6 ng / ml,P = 0.84),纤维蛋白原(305 +/- 72 vs 301 +/- 71 mg / dl,P = 0.33)或D-二聚体(0.49 +/- 0.24-0.51 +/- 0.28μg / ml,P = 0.70)水平。我们的数据表明,接受ACEIs或ARBs的患者不会因纤溶酶系统的生物标志物发生任何变化,而对肾素-血管紧张素-醛固酮系统有额外的药理抑制作用。

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