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白质完整性与运动功能:脑髓鞘形成与衰老过程中步态速度纵向变化之间的联系。

White matter integrity and motor function: a link between cerebral myelination and longitudinal changes in gait speed in aging.

作者信息

Gong Zhaoyuan, Faulkner Mary E, Akhonda Mohammad A B S, Guo Alex, Bae Jonghyun, Laporte John P, Church Sarah, D'Agostino Jarod, Bergeron Jan, Bergeron Christopher M, Ferrucci Luigi, Bouhrara Mustapha

机构信息

Laboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, BRC 05C-222, 251 Bayview Blvd., Baltimore, MD, 21224, USA.

Clinical Research Core, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.

出版信息

Geroscience. 2025 Apr;47(2):1441-1454. doi: 10.1007/s11357-024-01392-w. Epub 2024 Oct 30.

Abstract

Gait speed is a robust health biomarker in older adults, correlating with the risk of physical and cognitive impairments, including dementia. Myelination plays a crucial role in neurotransmission and consequently affects various functions, yet the connection between myelination and motor functions such as gait speed is not well understood. Understanding this link could offer insights into diagnosing and treating neurodegenerative diseases that impair mobility. This study analyzed 437 longitudinal observations from 138 cognitively unimpaired adults, aged 22 to 94 years, to investigate the relationship between myelin content and changes in gait speed over an average of 6.42 years. Myelin content was quantified using a novel multicomponent magnetic resonance relaxometry method, and both usual and rapid gait speeds (UGS, RGS) were measured following standard protocols. Adjusting for covariates, we found a significant fixed effect of myelin content on UGS and RGS. Longitudinally, lower myelin content was linked to a greater decline in UGS, particularly in brain regions associated with motor planning. These results suggest that changes in UGS may serve as a reliable marker of neurodegeneration, particularly in cognitively unimpaired adults. Interestingly, the relationship between myelin content and changes in RGS was only observed in a limited number of brain regions, although the reason for such local susceptibility remains unknown. These findings enhance our understanding of the critical role of myelination in gait performance in unimpaired adults and provide evidence of the interconnection between myelin content and motor function impairment.

摘要

步速是老年人健康状况的一个可靠生物标志物,与身体和认知功能障碍(包括痴呆症)的风险相关。髓鞘形成在神经传递中起着关键作用,因此会影响各种功能,但髓鞘形成与步速等运动功能之间的联系尚未得到充分理解。了解这种联系有助于深入了解诊断和治疗影响行动能力的神经退行性疾病。本研究分析了138名22至94岁认知未受损成年人的437项纵向观察数据,以调查髓鞘含量与平均6.42年期间步速变化之间的关系。使用一种新型多组分磁共振弛豫测量方法对髓鞘含量进行量化,并按照标准方案测量常规步速和快速步速(UGS、RGS)。在对协变量进行调整后,我们发现髓鞘含量对UGS和RGS有显著的固定效应。纵向来看,较低的髓鞘含量与UGS的更大下降有关,尤其是在与运动规划相关的脑区。这些结果表明,UGS的变化可能是神经退行性变的可靠标志物,尤其是在认知未受损的成年人中。有趣的是,仅在少数脑区观察到髓鞘含量与RGS变化之间的关系,尽管这种局部易感性的原因尚不清楚。这些发现加深了我们对髓鞘形成在未受损成年人步态表现中的关键作用的理解,并为髓鞘含量与运动功能损害之间的相互联系提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3afe/11979058/bc8d24bf1354/11357_2024_1392_Fig1_HTML.jpg

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