缬沙坦与氨氯地平对新诊断高血压患者vWf水平及N/L比值的影响比较

Murat Karaman, Sevket Balta, A Y Seyit Ahmet, Mustafa Cakar, Ilkin Naharci, Sait Demirkol, Turgay Celik, Zekeriya Arslan, Omer Kurt, Necmettin Kocak, Hakan Sarlak, Seref Demirbas, Fatih Bulucu, Ergun Bozoglu
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引用次数: 88

摘要

高血压患者外周血血管性血友病因子(vWf)和中性粒细胞/淋巴细胞(N/L)比值升高可能反映血管炎症。在本研究中,我们旨在探讨缬沙坦作为血管紧张素II受体拮抗剂和氨氯地平作为钙通道阻滞剂对原发性高血压患者vWf水平和N/L比值的影响。A组(n = 20人,平均年龄= 51.85±11.32 y)、B组(n = 26人,平均年龄= 49.12±14.12 y)分别给予钙通道阻滞剂(氨氯地平,5 ~ 10 mg/d)和血管紧张素受体阻滞剂(缬沙坦,80 ~ 320 mg/d)干预,观察高血压患者治疗前和治疗后第12周vWf水平和n /L比值,评价内皮功能障碍和血管炎症。在年龄、性别和身体质量指数(BMI)方面,各组之间没有统计学上的显著差异。vWf水平显著降低(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The comparative effects of valsartan and amlodipine on vWf levels and N/L ratio in patients with newly diagnosed hypertension.

High levels of circulating Von Willebrand factor (vWf) and increased neutrophil to lymphocyte (N/L) ratio may reflect vascular inflammation in hypertensive patients. In present study, we aimed to investigate the effects of valsartan as an angiotensin II receptor antagonist and amlodipine as a calcium channel blocker on the vWf levels and N/L ratio in patients with essential hypertension. Patients were randomized to one of the following intervention protocols: calcium channel blocker (amlodipine, 5-10 mg/day) as group A (n = 20 mean age = 51.85 ± 11.32 y) and angiotensine II receptor blocker (valsartan, 80-320 mg/day) as group B (n = 26 mean age = 49.12 ± 14.12 y). Endothelial dysfunction and vascular inflammation were evaluated with vWf levels and N/L ratio in hypertensive patients before treatment and after treatment in the 12th week. No statistically significant differences were found among the groups in terms of age, sex, and body mass index (BMI). There was a significant decrease in vWf levels (P < .001) and N/L ratio after treatment (P = .04, P < .001, respectively) in both the groups. Von Willebrand factor levels and N/L ratio are very important markers having a role in vascular inflammation and antihypertensive treatment with amlodipine and valsartan may improve cardiovascular outcomes by decreasing these biomarkers.

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