Association of Cerebrovascular Reactivity With 1-Year Imaging and Clinical Outcomes in Small Vessel Disease: An Observational Cohort Study.

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY Neurology Pub Date : 2024-12-10 Epub Date: 2024-11-05 DOI:10.1212/WNL.0000000000210008
Emilie Sleight, Michael S Stringer, Una Clancy, Carmen Arteaga-Reyes, Daniela Jaime Garcia, Angela C C Jochems, Stewart Wiseman, Maria Valdes Hernandez, Francesca M Chappell, Fergus N Doubal, Ian Marshall, Michael J Thrippleton, Joanna M Wardlaw
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Abstract

Background and objectives: In patients with cerebral small vessel disease (SVD), impaired cerebrovascular reactivity (CVR) is related to worse concurrent SVD burden, but less is known about cerebrovascular reactivity and long-term SVD lesion progression and clinical outcomes. We investigated associations between cerebrovascular reactivity and 1-year progression of SVD features and clinical outcomes.

Methods: Between 2018 and 2021, we recruited patients from the Edinburgh/Lothian stroke services presenting with minor ischemic stroke and SVD features as part of the Mild Stroke Study 3, a prospective observational cohort study (ISRCTN 12113543). We acquired 3T brain MRI at baseline and 1 year. At baseline, we measured cerebrovascular reactivity to 6% inhaled CO2 in subcortical gray matter, normal-appearing white matter, and white matter hyperintensities (WMH). At baseline and 1 year, we quantified SVD MRI features, incident infarcts, assessed stroke severity (NIH Stroke Scale), recurrent stroke, functional outcome (modified Rankin Scale), and cognition (Montreal Cognitive Assessment). We performed linear and logistic regressions adjusted for age, sex, and vascular risk factors, reporting the regression coefficients and odds ratios with 95% CIs.

Results: We recruited 208 patients of whom 163 (mean age and SD: 65.8 ± 11.2 years, 32% female) had adequate baseline CVR and completed the follow-up structural MRI. The median increase in WMH volume was 0.32 mL with (Q1, Q3) = (-0.48, 1.78) mL; 29% had a recurrent stroke or incident infarct on MRI. At 1 year, patients with lower baseline cerebrovascular reactivity in normal-appearing tissues had increased WMH (regression coefficient: B = -1.14 [-2.13, -0.14] log10 (%ICV) per %/mm Hg) and perivascular space volumes (B = -1.90 [-3.21, -0.60] log10 (%ROIV) per %/mm Hg), with a similar trend in WMH. CVR was not associated with clinical outcomes at 1 year.

Discussion: Lower baseline cerebrovascular reactivity predicted an increase in WMH and perivascular space volumes after 1 year. CVR should be considered in SVD future research and intervention studies.

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脑血管反应性与小血管疾病 1 年成像和临床结果的关系:一项观察性队列研究
背景和目的:在脑小血管疾病(SVD)患者中,脑血管反应性(CVR)受损与并发SVD负担加重有关,但人们对脑血管反应性与长期SVD病变进展和临床预后的了解较少。我们研究了脑血管反应性与 SVD 病变特征的 1 年进展和临床预后之间的关系:2018年至2021年期间,我们从爱丁堡/洛锡安卒中服务机构招募了出现轻微缺血性卒中和SVD特征的患者,作为前瞻性观察性队列研究 "轻微卒中研究3"(ISRCTN 12113543)的一部分。我们在基线和一年时采集了 3T 脑磁共振成像。基线时,我们测量了皮层下灰质、正常外观白质和白质高密度(WMH)对 6% 吸入二氧化碳的脑血管反应性。在基线和 1 年时,我们量化了 SVD MRI 特征、梗死事件、中风严重程度评估(NIH 中风量表)、复发性中风、功能结果(改良 Rankin 量表)和认知能力(蒙特利尔认知评估)。我们进行了线性回归和逻辑回归,并对年龄、性别和血管风险因素进行了调整,报告了回归系数和几率比及 95% CI:我们共招募了 208 名患者,其中 163 人(平均年龄和标码:65.8 ± 11.2 岁,32% 为女性)有足够的基线 CVR 并完成了随访结构磁共振成像。WMH体积增加的中位数为0.32 mL,(Q1, Q3) = (-0.48, 1.78) mL;29%的患者在磁共振成像中出现复发性卒中或梗死。1 年后,正常外观组织中基线脑血管反应性较低的患者 WMH 增加(回归系数:B = -1.14 [-2.13, -0.14] log10 (%ICV) per %/mm Hg)和血管周围空间体积(B = -1.90 [-3.21, -0.60] log10 (%ROIV) per %/mm Hg),WMH 的趋势相似。CVR与1年后的临床结果无关:讨论:较低的基线脑血管反应性预示着1年后WMH和血管周围空间体积的增加。在未来的SVD研究和干预研究中应考虑CVR。
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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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