医学
心脏病学
内科学
大脑中动脉
脑动脉
脑血流
血压
风险因素
磁共振成像
冲程(发动机)
血流
原发性高血压
舒张期
放射科
缺血
机械工程
工程类
作者
Marieke van den Kerkhof,Merel M. van der Thiel,Alida A. Postma,Robert J. van Oostenbrugge,Abraham A. Kroon,Jacobus F.A. Jansen,Walter H. Backes
出处
期刊:Hypertension
[Ovid Technologies (Wolters Kluwer)]
日期:2023-02-01
卷期号:80 (4): 802-810
被引量:7
标识
DOI:10.1161/hypertensionaha.122.19866
摘要
Hypertension alters the structure and function of cerebral blood vessels, and is an important risk factor for stroke and cerebral small vessel disease (cSVD). However, the pathophysiological process is not yet well understood. This study aimed to investigate the relationship between the pulsatility measures in small perforating arteries and hypertension, since hypertension-induced arterial stiffening may lead to a higher blood flow pulsatility and lower damping.We examined 28 patients with essential hypertension and 25 age- and sex-matched healthy controls (mean age: 63.4, range: 43-81 years, 26 males). Blood flow velocity waveforms were acquired in the lenticulostriate arteries (LSAs) and the middle cerebral artery using phase-contrast MRI at 7 Tesla. Several cSVD markers were scored. The velocity and pulsatility measures were compared between the hypertensives and controls.A higher pulsatility index (PI) in the LSAs and a lower damping factor (DF) was found in the hypertensive compared to the normotensive group (P=0.015, P=0.015, respectively), but no association was found for the PI in the middle cerebral artery. Higher systolic and mean arterial pressures were associated with higher PI in the LSA and DF. For diastolic blood pressure, only an association with a lower DF was found. Adjusting for cSVD score did not alter these relationships.This study shows a higher PI in the LSAs and a lower DF in subjects with hypertension, independent of cSVD presence. This supports the hypothesis that hypertension-induced arterial remodeling may alter the intracerebral blood flow velocity profiles, which could eventually contribute to cerebral tissue damage.URL: https://trialsearch.who.int/; Unique identifier: NL7537 and NL8798.
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