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奥美沙坦和氨氯地平对血压、内皮功能和血管炎症的影响。

Effects of olmesartan and amlodipine on blood pressure, endothelial function, and vascular inflammation.

机构信息

Division of Cardiovascular Medicine, Department of Medicine, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 830-0011, Japan.

Department of Pathophysiology and Therapeutics of Diabetic Vascular Complications, Kurume University School of Medicine, Kurume, Japan.

出版信息

J Nucl Cardiol. 2023 Aug;30(4):1613-1626. doi: 10.1007/s12350-023-03200-y. Epub 2023 Feb 3.

Abstract

BACKGROUND

Anti-hypertensive drugs can improve vascular endothelial function. However, the mechanism remains to be elucidated.

OBJECTIVES

This study sought to investigate mechanisms of anti-hypertensive drugs on improvement of vascular endothelial function in patients with essential hypertension.

METHODS

Forty-five patients (mean age 58.5 ± 11.2 years) with uncontrolled essential hypertension were randomly assigned to receive olmesartan, an angiotensin II type 1 receptor blocker (ARB) (N = 23), or amlodipine, a calcium channel blocker (CCB) (N = 22), for 6 months. Endothelial function was evaluated by flow-mediated dilatation (FMD) of the brachial artery. Vascular inflammation was measured by blood-normalized standardized uptake value, known as a target-to-background ratio (TBR) within the carotid arteries using 18F-fluorodeoxyglucose-positron emission tomography combined with computed tomography.

RESULTS

There were no significant differences of baseline clinical data between the ARB and CCB groups. Both anti-hypertensive drugs comparably lowered blood pressure and increased %FMD. TBR values were reduced by olmesartan (P < .001), while blood pressure variability was decreased by amlodipine (P = .004). Changes in %FMD from baseline (Δ%FMD) were inversely associated with ΔTBR in the olmesartan group (r = - .606, P = .003) and with Δsystolic blood pressure variability in the amlodipine group (r = - .434, P = .039).

CONCLUSION

Our study indicated that olmesartan and amlodipine could improve endothelial function in patients with essential hypertension in different manners, suppression of vascular inflammation, and decrease in blood pressure variability, respectively.

摘要

背景

抗高血压药物可改善血管内皮功能。然而,其机制仍有待阐明。

目的

本研究旨在探讨抗高血压药物改善原发性高血压患者血管内皮功能的机制。

方法

将 45 例(平均年龄 58.5±11.2 岁)未控制的原发性高血压患者随机分为奥美沙坦组(血管紧张素 II 型 1 型受体阻滞剂,n=23)和氨氯地平组(钙通道阻滞剂,n=22),分别接受 6 个月的治疗。采用肱动脉血流介导的扩张(FMD)评估内皮功能。通过 18F-氟脱氧葡萄糖正电子发射断层扫描与计算机断层扫描联合测量颈动脉内的标准化摄取值比值(TBR),即血液标准化标准化摄取值,来衡量血管炎症。

结果

ARB 组和 CCB 组的基线临床数据无显著差异。两种降压药均能降低血压,增加 FMD%。奥美沙坦组 TBR 值降低(P<0.001),而氨氯地平组血压变异性降低(P=0.004)。奥美沙坦组的 FMD 变化(ΔFMD)与 TBR 的变化呈负相关(r=−.606,P=0.003),与氨氯地平组的收缩压变异性变化呈负相关(r=−.434,P=0.039)。

结论

本研究表明,奥美沙坦和氨氯地平分别通过抑制血管炎症和降低血压变异性来改善原发性高血压患者的内皮功能。

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