老年人白质过度密集与运动认知风险综合征。

Joanna L Mergeche, Joe Verghese, Gilles Allali, Cuiling Wang, Olivier Beauchet, V G Pradeep Kumar, P S Mathuranath, Jennifer Yuan, Helena M Blumen
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摘要

简介运动性认知风险(MCR)综合征是最近描述的一种痴呆前期综合征,其特点是步态缓慢和认知抱怨,被认为是老年人认知能力下降和痴呆的预测因素。以往的研究表明,脑血管疾病与 MCR 有关。白质高密度(WMH)被认为是脑血管疾病的产物,与行动能力受损和认知能力受损有关。本研究旨在确定 MCR 是否与区域性 WMH 相关:方法:研究了两组跨文化的非痴呆老年人:174名参与者来自法国一家记忆诊所(62.1%为男性,平均年龄(70.7 ± 4.3)岁),184名参与者来自印度社区居民队列(55.4%为男性,平均年龄(66.2 ± 5.2)岁)。通过核磁共振成像(流体衰减反转恢复)FLAIR 序列对参与者的步态缓慢、认知症状和区域性 WMH 进行了评估:总体而言,20.7%的参与者符合MCR标准,72.9%的参与者在FLAIR上有WMH。在两个队列中,额叶、顶枕叶、颞叶、基底节、小脑或脑干的 WMH 均与 MCR 无关:结论:在所研究的参与者样本中,WMH 与 MCR 并无明显关联,这表明 MCR 可能是其他脑血管病理生理机制或机制组合的结果。
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White Matter Hyperintensities in Older Adults and Motoric Cognitive Risk Syndrome.

Introduction: Motoric cognitive risk (MCR) syndrome is a recently described pre-dementia syndrome characterized by slow gait and cognitive complaints that has been implicated as a predictor of cognitive decline and dementia in older adults. Previous work suggests that cerebrovascular disease is associated with MCR. White matter hyperintensities (WMH) are postulated to be a product of cerebrovascular disease, and have been associated with impaired mobility and impaired cognition. This study aimed to determine if MCR is associated with regional WMH.

Methods: Two cross-cultural cohorts of non-demented older adults were examined: 174 from a French memory clinic (62.1% male, mean age 70.7 ± 4.3 years) and 184 from an Indian community-dwelling cohort (55.4% male, mean age 66.2 ± 5.2 years). Participants were evaluated for slow gait, cognitive complaints, and regional WMH via MRI (fluid attenuated inversion recovery) FLAIR sequence.

Results: Overall, 20.7% of participants met criteria for MCR, and 72.9% of participants had WMH on FLAIR. WMH in the frontal, parieto-occipital, temporal, basal ganglia, cerebellum, or brainstem were not associated with MCR in either of the two cohorts.

Conclusion: WMH was not significantly associated with MCR in this studied sample of participants, suggesting that other cerebrovascular pathophysiological mechanisms, or combination of mechanisms, might underlie MCR.

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