Associations between brain structure and dual decline in gait and cognition

IF 3.7 3区 医学 Q2 GERIATRICS & GERONTOLOGY
Sadhani Karunarathna , Monique Breslin , Jane Alty , Richard Beare , Taya A. Collyer , Velandai K. Srikanth , James Scott McDonald , Michele L. Callisaya
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Abstract

Dual decline in gait and cognition is associated with an increased risk of dementia, with combined gait and memory decline exhibiting the strongest association. To better understand the underlying pathology, we investigated the associations of baseline brain structure with dual decliners using three serial gait speed and cognitive assessments in memory, processing speed-attention, and verbal fluency. Participants (n=267) were categorized based on annual decline in gait speed and cognitive measures. Lower gray and white matter volume and higher white matter hyperintensity volume increased the risk of being a dual decliner in gait and both the memory and processing speed-attention groups (all p < 0.05). Lower hippocampal volume (p = 0.047) was only associated with dual decline in gait and memory group. No brain structures were correlated with dual decline in gait and verbal fluency. These results suggest that neurodegenerative pathology and white matter hyperintensities are involved in dual decline in gait and both memory and processing speed-attention. Smaller hippocampal volume may only contribute to dual decline in gait and memory.

大脑结构与步态和认知能力双重衰退之间的关系
步态和认知能力的双重衰退与痴呆症风险的增加有关,其中步态和记忆力的综合衰退表现出最强的关联性。为了更好地了解潜在的病理,我们使用三个序列的步速和记忆力、处理速度-注意力和语言流畅性的认知评估,研究了基线大脑结构与双重衰退者的关联。根据步速和认知测量的年下降率对参与者(n=267)进行了分类。较低的灰质和白质体积以及较高的白质高密度体积会增加步态以及记忆和处理速度-注意力两组双重下降的风险(所有 p < 0.05)。海马体积较小(p = 0.047)仅与步态和记忆组的双重衰退有关。没有大脑结构与步态和语言流畅性的双重下降相关。这些结果表明,神经退行性病变和白质高密度与步态、记忆力和处理速度-注意力的双重下降有关。海马体积较小可能只导致步态和记忆力的双重下降。
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来源期刊
Neurobiology of Aging
Neurobiology of Aging 医学-老年医学
CiteScore
8.40
自引率
2.40%
发文量
225
审稿时长
67 days
期刊介绍: Neurobiology of Aging publishes the results of studies in behavior, biochemistry, cell biology, endocrinology, molecular biology, morphology, neurology, neuropathology, pharmacology, physiology and protein chemistry in which the primary emphasis involves mechanisms of nervous system changes with age or diseases associated with age. Reviews and primary research articles are included, occasionally accompanied by open peer commentary. Letters to the Editor and brief communications are also acceptable. Brief reports of highly time-sensitive material are usually treated as rapid communications in which case editorial review is completed within six weeks and publication scheduled for the next available issue.
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