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      Hypertension-Induced Cerebral Small Vessel Disease Leading to Cognitive Impairment Translated title: 高血压相关性脑小血管病引起认知障碍

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          Abstract

          Objective:

          Alzheimer's disease and vascular dementia are responsible for more than 80% of dementia cases. These two conditions share common risk factors including hypertension. Cerebral small vessel disease (CSVD) is strongly associated with both hypertension and cognitive impairment. In this review, we identify the pathophysiological changes in CSVD that are caused by hypertension and further explore the relationship between CSVD and cognitive impairment.

          Data Sources:

          We searched and scanned the PubMed database for recently published literatures up to December 2017. We used the keywords of “hypertension”, “cerebral small vessel disease”, “white matter lesions”, “enlarged perivascular spaces”, “lacunar infarcts”, “cerebral microbleeds”, and “cognitive impairment” in the database of PubMed.

          Study Selection:

          Articles were obtained and reviewed to analyze the hypertension-induced pathophysiological changes that occur in CSVD and the correlation between CSVD and cognitive impairment.

          Results:

          In recent years, studies have demonstrated that hypertension-related changes (e.g., small vascular lesions, inflammatory reactions, hypoperfusion, oxidative stress, damage to autoregulatory processes and the blood-brain barrier, and cerebral amyloid angiopathy) can occur over time in cerebral small vessels, potentially leading to lower cognitive function when blood pressure (BP) control is poor or lacking. Both isolated and co-occurrent CSVD can lead to cognitive deterioration, and this effect may be attributable to a dysfunction in either the cholinergic system or the functionality of cortical and subcortical tracts.

          Conclusions:

          We explore the currently available evidence about the hypertensive vasculopathy and inflammatory changes that occur in CSVD. Both are vital prognostic indicators of the development of cognitive impairment. Future studies should be performed to validate the relationship between BP levels and CSVD progression and between the numbers, volumes, and anatomical locations of CSVD and cognitive impairment.

          摘要

          目的:

          80%痴呆为阿尔茨海默病和/或血管性痴呆,两者的共同危险因素包括高血压。脑小血管病(cerebral small vessel disease,CSVD)与高血压和认知功能障碍均密切相关。本文对高血压引起CSVD的病理机制及CSVD与认知功能障碍的额关系进行综述,以期更好的了解CSVD与高血压、认知障碍的关系。

          方法:

          通过使用高血压、脑小血管病、白质病变、扩大的血管周围间隙、腔隙性脑梗塞、脑微出血和认知障碍等关键词检索PubMed数据库最新文献。对相关文章进行回顾分析,整理并分析高血压引起CSVD的病理生理变化及CSVD与认知障碍的关系。

          结果:

          近年研究表明,高血压相关性病理改变:小血管病变、炎症反应、氧化应激、低灌注,自身调节障碍,血脑屏障破坏及脑淀粉样血管病等可致CSVD,进而引起认知功能障碍。血压控制欠佳时,单一或多种CSVD可致认知功能下降,这种作用可能是由于胆碱能系统功能障碍或皮质与皮质下传导束功能紊乱所致。

          结论:

          高血压相关性血管病变和炎症反应可引起CSVD。两者均是认知功能障碍发展的重要预后指标。不同解剖部位CSVD,CSVD数量等对认知功能领域的影响尚存在争议。血压水平与EPVS的发生发展,CSVD数量、体积及解剖位置的变化与认知功能障碍的关系需进一步探索。

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          Most cited references47

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          Hypertension: a harbinger of stroke and dementia.

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            MRI-visible perivascular spaces in cerebral amyloid angiopathy and hypertensive arteriopathy.

            To assess MRI-visible enlarged perivascular spaces (EPVS) burden and different topographical patterns (in the centrum semiovale [CSO] and basal ganglia [BG]) in 2 common microangiopathies: cerebral amyloid angiopathy (CAA) and hypertensive arteriopathy (HA).
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              Enlarged perivascular spaces and cerebral small vessel disease

              Background and aims Enlarged perivascular spaces (also known as Virchow–Robin spaces) on T2-weighted brain magnetic resonance imaging are common, but their etiology, and specificity to small vessel as opposed to general cerebrovascular disease or ageing, is unclear. We tested the association between enlarged perivascular spaces and ischemic stroke subtype, other markers of small vessel disease, and common vascular risk factors. Methods We prospectively recruited patients with acute stroke, diagnosed and subtyped by a stroke physician using clinical features and brain magnetic resonance imaging. A neuroradiologist rated basal ganglia and centrum semiovale enlarged perivascular spaces on a five-point scale, white matter lesions, recent and old infarcts, and cerebral atrophy. We assessed associations between basal ganglia-, centrum semiovale- and total (combined basal ganglia and centrum semiovale) enlarged perivascular spaces, stroke subtype, white matter lesions, atrophy, and vascular risk factors. Results Among 298 patients (mean age 68 years), after adjusting for vascular risk factors and white matter lesions, basal ganglia–enlarged perivascular spaces were associated with increasing age (P = 0·001), centrum semiovale–enlarged perivascular spaces (P < 0·001), cerebral atrophy (P = 0·03), and lacunar stroke subtype (P = 0·04). Centrum semiovale–enlarged perivascular spaces were associated mainly with basal ganglia–enlarged perivascular spaces. Total enlarged perivascular spaces were associated with increasing age (P = 0·01), deep white matter lesions (P = 0·005), and previous stroke (P = 0·006). Conclusions Enlarged perivascular spaces are associated with age, lacunar stroke subtype and white matter lesions and should be considered as another magnetic resonance imaging marker of cerebral small vessel disease. Further evaluation of enlarged perivascular spaces in studies of ageing, stroke, and dementia is needed to determine their pathophysiological importance.
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                Author and article information

                Journal
                Chin Med J (Engl)
                Chin. Med. J
                CMJ
                Chinese Medical Journal
                Medknow Publications & Media Pvt Ltd (India )
                0366-6999
                05 March 2018
                : 131
                : 5
                : 615-619
                Affiliations
                [1 ]Graduate School, Hebei Medical University, Shijiazhuang, Hebei 050017, China
                [2 ]Department of Neurology, Hebei General Hospital, Shijiazhuang, Hebei 050051, China
                Author notes
                Address for correspondence: Prof. Pei-Yuan Lyu, Department of Neurology, Hebei General Hospital, 348 Heping West Road, Shijiazhuang, Hebei 050051, China E-Mail: peiyuanlu@ 123456163.com
                Article
                CMJ-131-615
                10.4103/0366-6999.226069
                5850681
                29483399
                2359de6a-b37f-4754-aa52-368277b66cb1
                Copyright: © 2018 Chinese Medical Journal

                This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

                History
                : 06 November 2017
                Categories
                Review Article

                cerebral microbleeds,cerebral small vessel disease,cognitive impairment,hypertension

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