Impact of white matter hyperintensity regression on global cognition, processing speed and executive function

IF 1.9 Q3 CLINICAL NEUROLOGY
Angela Jochems , Susana Muñoz Maniega , Una Clancy , Daniela Jaime Garcia , Carmen Arteaga , Mariadel C. Valdés Hernández , Will Hewins , Rachel Penman , Ellen Backhouse , Stewart Wiseman , Michael Thrippleton , Michael Stringer , Francesca Chappell , Fergus Doubal , Joanna Wardlaw
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引用次数: 0

Abstract

Introduction

White matter hyperintensities (WMH) are related to cognitive decline, particularly processing speed and executive functioning (EF). However, all cognitive domains might be affected. WMH can regress and this might have positive consequences for cognition, but the effects of WMH regression on cognition are unknown. This study aims to assess whether changes in global cognition, processing speed and EF are related to progressing and regressing WMH.

Methods

We recruited mild, non-disabling, ischemic stroke patients with sporadic small vessel disease. They underwent MRI and cognitive assessment within 3 months post-stroke and 1 year later. Cognitive assessment included MoCA (global cognition; score 0-30), trail making test (TMT) A (processing speed; seconds) and TMT B (EF; seconds). WMH volumes are reported as % intracranial volume (ICV). WMH volume change (%ICV) is defined as WMH volume difference between baseline and 1 year. We calculated quintiles (Q) of WMH volume change to group volume change. We performed three linear mixed models, with MoCA, TMT-A and B as outcomes, to assess relationships over time with quintile of WMH volume change. Predictors in addition to quintile are age, sex, premorbid intelligence (NART), stroke severity (NIHSS). Extra predictor for TMT-B analysis is the TMT-A time to correct for speed.

Results

202 participants had WMH change volumes available (mean age: 66.03 years [SD=11.15), 33% female]. Q1 reflect greatest WMH volume reduction and Q5 greatest volume increase, while Q3 is lowest overall volume change (Figure 1). MoCA score increased over time (Figure 2). Older age (std. B [std. 95%CI]: -0.303 [-0.400, -0.206]), worse NART (-0.463 [-0.557, -0.368]), increasing NIHSS (-0.208 [-0.286, -0.130]) and more WMH increase (Q5; -0.513 [-0.814, -0.211]) predict lower MoCA. Older age (0.257 [0.135, 0.380]), worse NART (0.259 [0.139, 0.378]) and higher NIHSS (0.152 [0.078, 0.226]) predict worse TMT-A time (Figure 3A). Older age (0.224 [0.132, 0.316]), worse NART (0.295 [0.207, 0.383]), worse TMT-A (0.469 [0.384, 0.555]), worsening WMH volume (Q2; 0.382 [0.115, 0.0.649] and Q5; 0.425 [0.150, 0.699]) predict worse TMT-B time (Figure 3B).

Discussion

More WMH progression independently predicts worse global cognition and EF but not processing speed. WMH regression (Q1) was not related to worsening or improving global cognition, processing speed and EF. Cognitive consequences of WMH regression might be comparable to stable WMH (Q3).

白质高密度回归对整体认知、处理速度和执行功能的影响
导言白质过密(WMH)与认知能力下降有关,尤其是处理速度和执行功能(EF)。然而,所有认知领域都可能受到影响。WMH可以消退,这可能会对认知能力产生积极影响,但WMH消退对认知能力的影响尚不清楚。本研究旨在评估全局认知、处理速度和 EF 的变化是否与 WMH 的进展和消退有关。他们在中风后 3 个月内和 1 年后接受了核磁共振成像和认知评估。认知评估包括MoCA(总体认知;0-30分)、路径制作测试(TMT)A(处理速度;秒)和TMT B(EF;秒)。WMH体积以颅内容积(ICV)百分比报告。WMH体积变化(%ICV)定义为基线与1年之间的WMH体积差异。我们计算了 WMH 体积变化的五分位数(Q)与群体体积变化的比率。我们以 MoCA、TMT-A 和 B 为结果,建立了三个线性混合模型,以评估 WMH 体积变化五分位数与时间的关系。除五分位数外,还有年龄、性别、病前智力(NART)、卒中严重程度(NIHSS)等预测因素。结果202名参与者有WMH变化体积(平均年龄:66.03岁[SD=11.15],33%为女性)。Q1 反映了最大的 WMH 体积减少,Q5 反映了最大的体积增加,而 Q3 是总体体积变化最小的(图 1)。MoCA 评分随时间推移而增加(图 2)。年龄越大(std. B [std.95%CI]:-0.303 [-0.400, -0.206])、NART 越差(-0.463 [-0.557, -0.368])、NIHSS 越高(-0.208 [-0.286, -0.130])以及 WMH 增加越多(Q5;-0.513 [-0.814, -0.211]),预示 MoCA 越低。年龄越大(0.257 [0.135, 0.380])、NART 越差(0.259 [0.139, 0.378])和 NIHSS 越高(0.152 [0.078, 0.226]),预测 TMT-A 时间越短(图 3A)。年龄较大(0.224 [0.132,0.316])、NART 较差(0.295 [0.207,0.383])、TMT-A 较差(0.469 [0.384,0.555])、WMH 体积恶化(Q2;0.382 [0.115,0.0.649] 和 Q5;0.425 [0.150,0.699])可预测更差的 TMT-B 时间(图 3B).讨论更多的 WMH 进展可独立预测更差的全局认知和 EF,但不能预测处理速度。WMH消退(Q1)与整体认知、处理速度和EF的恶化或改善无关。WMH消退对认知的影响可能与稳定的WMH(Q3)相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cerebral circulation - cognition and behavior
Cerebral circulation - cognition and behavior Neurology, Clinical Neurology
CiteScore
2.00
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审稿时长
14 weeks
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