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Peak width of skeletonized mean diffusivity and its association with age-related cognitive alterations and vascular risk factors

Only two studies investigated the associations between peak width of skeletonized mean diffusivity (PSMD) and age-related cognitive alterations, whereas none of the studies investigated the association with vascular risk factors. We evaluated 801 stroke- and dementia-free elderlies with baseline and...

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Published in:Alzheimer's & dementia : diagnosis, assessment & disease monitoring assessment & disease monitoring, 2019-12, Vol.11 (1), p.721-729
Main Authors: Lam, Bonnie Yin Ka, Leung, Kam Tat, Yiu, Brian, Zhao, Lei, Biesbroek, J. Matthijs, Au, Lisa, Tang, Yumi, Wang, Kai, Fan, Yuhua, Fu, Jian-Hui, Xu, Qun, Song, Haiqing, Tian, Xiaolin, Chu, Winnie Chiu Wing, Abrigo, Jill, Shi, Lin, Ko, Ho, Lau, Alexander, Duering, Marco, Wong, Adrian, Mok, Vincent Chung Tong
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Language:English
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Summary:Only two studies investigated the associations between peak width of skeletonized mean diffusivity (PSMD) and age-related cognitive alterations, whereas none of the studies investigated the association with vascular risk factors. We evaluated 801 stroke- and dementia-free elderlies with baseline and 3-year follow-up assessments. Regression analyses were used to assess the association between age-related cognitive functions and PSMD. Simple mediation models were used to study the mediation effect of PSMD between vascular risk factors and age-related cognitive outcomes. PSMD was negatively associated with processing speed at baseline and negatively associated with processing and memory scores at 3-year follow-up. The association between vascular risk factors and age-related cognition was mediated by PSMD, as well as other diffusion tensor imaging markers. PSMD is preferred over other diffusion tensor imaging markers as it is sensitive to age-related cognitive alterations and calculation is fully automated. PSMD is proposed as a research tool to monitor age-related cognitive alterations.
ISSN:2352-8729
2352-8729
DOI:10.1016/j.dadm.2019.09.003