测试结构断裂假说:髓鞘含量与健康老年人的记忆力有关

IF 3.7 3区 医学 Q2 GERIATRICS & GERONTOLOGY Neurobiology of Aging Pub Date : 2024-05-23 DOI:10.1016/j.neurobiolaging.2024.05.013
Andrea Mendez Colmenares , Michael L. Thomas , Charles Anderson , David B. Arciniegas , Vince Calhoun , In-Young Choi , Arthur F. Kramer , Kaigang Li , Jongho Lee , Phil Lee , Agnieszka Z. Burzynska
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引用次数: 0

摘要

引言认知老化的 "结构断裂 "假说认为白质(WM),尤其是髓鞘的退化会导致认知能力下降,但体内证据尚无定论。方法我们使用髓鞘水成像和弥散张量成像检查了141名健康参与者(20-79岁)的WM微结构的年龄差异。我们使用弗吉尼亚认知老化项目和美国国立卫生研究院工具箱(NIH Toolbox®)生成了记忆力、处理速度和执行功能的复合数据。结果体素分析表明,在控制了年龄、性别和教育程度之后,髓鞘水分数(MWF)较低与记忆力下降有关,主要是在前额叶WM、胼胝体基底和内囊后缘。在结构方程模型中,前额叶白质和胼胝体底部的水份含量对年龄对记忆力的影响有显著的中介作用,而分数各向异性(FA)则没有。
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Testing the structural disconnection hypothesis: Myelin content correlates with memory in healthy aging

Introduction

The "structural disconnection" hypothesis of cognitive aging suggests that deterioration of white matter (WM), especially myelin, results in cognitive decline, yet in vivo evidence is inconclusive.

Methods

We examined age differences in WM microstructure using Myelin Water Imaging and Diffusion Tensor Imaging in 141 healthy participants (age 20–79). We used the Virginia Cognitive Aging Project and the NIH Toolbox® to generate composites for memory, processing speed, and executive function.

Results

Voxel-wise analyses showed that lower myelin water fraction (MWF), predominantly in prefrontal WM, genu of the corpus callosum, and posterior limb of the internal capsule was associated with reduced memory performance after controlling for age, sex, and education. In structural equation modeling, MWF in the prefrontal white matter and genu of the corpus callosum significantly mediated the effect of age on memory, whereas fractional anisotropy (FA) did not.

Discussion

Our findings support the disconnection hypothesis, showing that myelin decline contributes to age-related memory loss and opens avenues for interventions targeting myelin health.

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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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