首页> 外文期刊>Journal of Internal Medicine >Irbesartan reduces common carotid artery intima-media thickness in hypertensive patients when compared with atenolol: the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA) study.
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Irbesartan reduces common carotid artery intima-media thickness in hypertensive patients when compared with atenolol: the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA) study.

机译:与阿替洛尔相比,厄贝沙坦降低了高血压患者的颈总动脉内膜中层厚度:瑞典对厄贝沙坦左室肥大的研究与阿替洛尔的比较。

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BACKGROUND AND PURPOSE: Angiotensin II promotes cell growth and has been implicated in the development and maintenance of left ventricular (LV) hypertrophy and of structural vascular changes. We wished to examine whether an angiotensin receptor blocker (ARB) would influence structural vascular changes beyond the effects of blood pressure reduction. METHODS: Hypertensive patients with LV hypertrophy (age 55 +/- 9 years, blood pressure 162 +/- 19/104 +/- 8 mmHg, LV mass index 148 +/- 31 g m(-2); mean +/- SD) were randomized double-blind to the ARB irbesartan (n=52) or the beta(1) receptor blocker atenolol (n=56) for 48 weeks. Ultrasonography of the left and right common carotid artery (CCA) and echocardiography were performed at week 0 and 48. RESULTS: With similar reductions in blood pressure, CCA intima-media thickness (IMT) was reduced by irbesartan (from 0.92 +/- 0.14 by 0.01 +/- 0.10 mm, NS), whereas it was increased by atenolol (from 0.94 +/- 0.21 by 0.03 +/- 0.12 mm, P=0.018; P=0.002 between groups). CCA lumen diameter was less reduced by irbesartan than by atenolol. Thus, CCA intima-media area was reduced by irbesartan (from 21.3 +/- 5.0 by 0.90 +/- 2.45 mm(2), P=0.034) but not by atenolol (from 21.3 +/- 6.1 by 0.18 +/- 2.71 mm(2), NS; P=0.037 between groups). Changes in CCA IMT or area did not relate to changes in LV mass. CONCLUSIONS: The favourable effects by irbesartan on CCA IMT with an outward vascular remodelling suggest that angiotensin II mediates structural vascular changes, beyond the effects of blood pressure. This may be important in the prevention of cerebrovascular events.
机译:背景与目的:血管紧张素II促进细胞生长,并与左心室(LV)肥大和结构性血管变化的发生和维持有关。我们希望检查血管紧张素受体阻滞剂(ARB)是否会影响降压作用之外的结构性血管变化。方法:高血压左室肥厚的患者(年龄55 +/- 9岁,血压162 +/- 19/104 +/- 8 mmHg,左室质量指数148 +/- 31 gm(-2);平均+/- SD )随机双盲接受ARB厄贝沙坦(n = 52)或beta(1)受体阻滞剂阿替洛尔(n = 56)48周。左,右颈总动脉(CCA)的超声检查和超声心动图检查分别在第0周和第48周进行。结果:随着血压的降低,厄贝沙坦降低了CCA的内膜中层厚度(IMT)(从0.92 +/- 0.14起)增加了0.01 +/- 0.10毫米,NS),而阿替洛尔则将其增加了(从0.94 +/- 0.21增加了0.03 +/- 0.12毫米,P = 0.018;组间P = 0.002)。厄贝沙坦比阿替洛尔减少的CCA管腔直径。因此,厄贝沙坦降低了CCA内膜中层面积(从21.3 +/- 5.0降低了0.90 +/- 2.45 mm(2),P = 0.034),但没有被阿替洛尔降低(从21.3 +/- 6.1降低了0.18 +/- 2.71 mm(2),NS;组之间P = 0.037)。 CCA IMT或面积的变化与左室重量的变化无关。结论:厄贝沙坦对CCA IMT具有有利的作用,具有向外的血管重塑,提示血管紧张素II介导了结构性血管变化,超出了血压的影响。这对于预防脑血管事件可能很重要。

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