Ishibashi Ken, Kurisu Satoshi, Kato Yasuko, Mitsuba Naoya, Dohi Yoshihiro, Nishioka Kenji, Kihara Yasuki
Department of Cardiovascular Medicine, Hiroshima University Graduate School of Biomedical Sciences, 1-2-3, Kasumi-cho, Minami-ku, Hiroshima, Japan.
Heart Vessels. 2013 Jan;28(1):7-11. doi: 10.1007/s00380-011-0204-7. Epub 2011 Nov 2.
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 μg/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.
阿利吉仑是一种新型降压药,为口服直接肾素抑制剂。我们评估了阿利吉仑对正在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(ARBs)治疗的冠心病患者纤溶系统的影响。我们研究了17例冠心病患者,尽管接受了ACEIs或ARBs治疗,但其收缩压仍高于130 mmHg。将阿利吉仑(150 mg)添加到ACEIs或ARBs中,并持续使用6周。6周后,阿利吉仑显著降低了收缩压(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)。然而,它并未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±0.28 μg/ml,P = 0.70)水平。我们的数据表明,在对肾素-血管紧张素-醛固酮系统进行额外的药物抑制时,接受ACEIs或ARBs治疗的患者纤溶系统生物标志物预计不会有任何变化。