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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Plasma fibrin clot properties in arterial hypertension and their modification by antihypertensive medication
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Plasma fibrin clot properties in arterial hypertension and their modification by antihypertensive medication

机译:高血压患者血浆纤维蛋白凝块的特性及其通过降压药的治疗

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摘要

Background: We sought to determine plasma fibrin clot properties in hypertensive subjects and to evaluate potential effects of antihypertensive therapy on these parameters. Patients and Methods: Sixty-one patients (30 men, 31 women) with essential arterial hypertension stage 1 or 2 (aged 46.6 ± 14.4 years), free of clinically evident vascular disease, were randomly allocated for monotherapy with one of the 5 antihypertensive agents, i.e. quinapril, losartan, amlodipine, hydrochlorothiazide, or bisoprolol. Plasma fibrin clot permeability, turbidimetry and efficiency of fibrinolysis were investigated at baseline and after 6 months of therapy. Results: Baseline systolic blood pressure in a 24-hour ambulatory monitoring was correlated with clot permeability (r = - 0.37, p < 0.05), lysis time (r = 0.42, p < 0.05) and maximal D-dimer concentration released from clots (r = 0.45, p < 0.05). Antihypertensive treatment resulted in reduction of systolic/diastolic blood pressure in office measurements and 24-hour monitoring (all p < 0.001), accompanied by an increase in clot permeability, reduction in clot lysis time and lower maximal D-dimer concentration released from fibrin clots (all p < 0.05). No changes were observed in turbidimetric variables. Posttreatment changes in plasma fibrin clot properties were related to reductions in systolic blood pressure, complement component C3 and total cholesterol. Conclusions: Reduction in systolic blood pressure during antihypertensive treatment leads to increased plasma fibrin clot permeation and susceptibility to lysis, which might be a novel antithrombotic mechanism of blood pressure lowering therapy.
机译:背景:我们试图确定高血压受试者的血浆纤维蛋白凝块特性,并评估抗高血压治疗对这些参数的潜在影响。患者和方法:61名患有原发性高血压期1或2期(年龄46.6±14.4岁),无临床明显血管疾病的患者(30例男性,31例女性)被随机分配用于5种降压药之一的单药治疗即奎那普利,氯沙坦,氨氯地平,氢氯噻嗪或比索洛尔。在基线和治疗6个月后研究血浆纤维蛋白凝块的渗透性,比浊法和纤维蛋白溶解的效率。结果:24小时动态监测中的基线收缩压与血凝块通透性(r =-0.37,p <0.05),裂解时间(r = 0.42,p <0.05)和血凝块释放的最大D-二聚体浓度相关( r = 0.45,p <0.05)。降压治疗可减少办公室测量和24小时监测中的收缩压/舒张压(均p <0.001),并伴随血凝块通透性增加,血凝块溶解时间减少和血纤蛋白血凝块释放的最大D-二聚体浓度降低。 (所有p <0.05)。比浊变量没有观察到变化。治疗后血浆纤维蛋白凝块特性的变化与收缩压,补体成分C3和总胆固醇的降低有关。结论:降压治疗期间收缩压的降低导致血浆纤维蛋白凝块渗透增加和对溶解的敏感性,这可能是降压治疗的一种新的抗血栓形成机制。

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