首页> 外文期刊>Journal of human hypertension >Angiotensin II receptor blockade with valsartan decreases plasma osteopontin levels in patients with essential hypertension.
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Angiotensin II receptor blockade with valsartan decreases plasma osteopontin levels in patients with essential hypertension.

机译:缬沙坦可阻断血管紧张素II受体,从而降低原发性高血压患者的血浆骨桥蛋白水平。

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Osteopontin (OPN) has recently emerged as a key factor in both vascular remodelling and development of atherosclerosis. It has been reported that OPN is regulated by the renin-angiotensin-aldosterone system (RAAS). The aim of this study was to clarify the effect of angiotensin II receptor blockade with valsartan on plasma OPN levels in patients with essential hypertension (EHT). Forty-six patients (mean age, 64+/-11 years) with EHT were randomly assigned to treatment with amlodipine or valsartan. There were no significant differences in baseline clinical characteristics between the two groups. Blood sampling and blood pressure evaluation were performed before and after 24 weeks of treatment. After 24 weeks, both systolic blood pressure (SBP) and diastolic blood pressure (DBP) were decreased significantly and by the same degree in each treatment group. However, valsartan but not amlodipine decreased plasma OPN levels (baseline and 24-week data-valsartan: 614+/-224 ng ml(-1), 472+/-268 ng ml(-1), P=0.006; amlodipine: 680+/-151 ng ml(-1), 687+/-234 ng ml(-1), P>0.999). A positive correlation between the reduction in OPN and the log natural (ln) C-reactive protein (CRP) was seen in the valsartan-treated group. Stepwise regression analysis showed that treatment with valsartan and the reduction of ln CRP were associated with the reduction in OPN levels, and this association was independent of the reduction in SBP or aldosterone levels (valsartan: beta=0.332, P=0.026; ln CRP reduction: beta=0.366, P=0.015). These results suggest that suppression of the RAAS and inflammation may decrease plasma OPN levels.
机译:骨桥蛋白(OPN)最近已成为血管重构和动脉粥样硬化发展的关键因素。据报道,OPN受肾素-血管紧张素-醛固酮系统(RAAS)的调节。这项研究的目的是阐明缬沙坦对血管紧张素II受体的阻断对原发性高血压(EHT)患者血浆OPN水平的影响。 46例EHT患者(平均年龄64 +/- 11岁)被随机分配接受氨氯地平或缬沙坦治疗。两组之间的基线临床特征无显着差异。在治疗24周之前和之后进行血液采样和血压评估。 24周后,每个治疗组的收缩压(SBP)和舒张压(DBP)均显着降低,幅度均相同。但是,缬沙坦而非氨氯地平不会降低血浆OPN水平(基线和24周数据-缬沙坦:614 +/- 224 ng ml(-1),472 +/- 268 ng ml(-1),P = 0.006;氨氯地平: 680 +/- 151 ng ml(-1),687 +/- 234 ng ml(-1),P> 0.999)。在缬沙坦治疗组中,OPN减少与对数天然(ln)C反应蛋白(CRP)之间呈正相关。逐步回归分析表明,缬沙坦治疗和ln CRP降低与OPN水平降低相关,并且这种关联与SBP或醛固酮水平的降低无关(缬沙坦:beta = 0.332,P = 0.026; ln CRP降低:beta = 0.366,P = 0.015)。这些结果表明抑制RAAS和炎症可能会降低血浆OPN水平。

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