2nd Medical Clinic-Gastroenterology, University Hospital, Splaiul Independentei no. 169, Bucharest, Romania.
J Gastrointestin Liver Dis. 2006 Dec;15(4):337-42.
The aim of the study was to assess the effects of valsartan, a new generation angiotensin II receptor antagonist, on portal and systemic hemodynamics and on renal function in cirrhosis.
Eighty patients with cirrhosis and portal hypertension were divided in two groups as follows: group I - 40 patients who received valsartan (Diovan) 80 mg /day for 7 days and group II - 40 patients who received placebo. All the patients had hemodynamic, endocrine and renal parameters measured on day 0 and 7. The following were assessed: creatinine clearance, lithium clearance, plasma renin activity, concentration of plasma aldosteron and sodium homeostasis. Hemodynamic effects were assessed sonographically by portal flow volume and velocity evaluation, and mean arterial blood pressure.
Valsartan increased the portal blood flow and the portal velocity (p < 0.01). These changes occurred without any significant changes in blood pressure and renal function or the glomerular filtration rate, compared with controls (p > 0.05). Valsartan also reduced the concentration of plasma aldosteron (p < 0.01) and increased the urinary sodium excretion (p < 0.001).
A one week treatment with valsartan in cirrhotic patients with portal hypertension determines an increase in natriuresis, which could be regarded as beneficial and changes in the portal hemodynamics which might be speculated to represent a reduction of portal resistance.
本研究旨在评估新型血管紧张素Ⅱ受体拮抗剂缬沙坦对肝硬化患者门静脉和全身血液动力学及肾功能的影响。
80 例肝硬化伴门静脉高压患者分为两组:I 组(40 例)给予缬沙坦(代文)80mg/天,共 7 天;II 组(40 例)给予安慰剂。所有患者在第 0 天和第 7 天测量血流动力学、内分泌和肾功能参数。评估内容如下:肌酐清除率、锂清除率、血浆肾素活性、血浆醛固酮浓度和钠稳态。通过门静脉血流量和流速评估及平均动脉血压超声评估血流动力学效应。
缬沙坦增加了门静脉血流量和门静脉速度(p<0.01)。与对照组相比(p>0.05),这些变化在血压、肾功能或肾小球滤过率没有明显变化的情况下发生。缬沙坦还降低了血浆醛固酮浓度(p<0.01)并增加了尿钠排泄(p<0.001)。
在肝硬化伴门静脉高压患者中,用缬沙坦治疗一周可增加利钠作用,这可能被认为是有益的,同时也改变了门静脉血液动力学,这可能表明门静脉阻力降低。