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Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease
Glymphatic dysfunction has been linked to cognitive decline in several neurodegenerative diseases. In cerebral small vessel disease (CSVD), the mechanism of white matter hyperintensities (WMH)-related cognitive impairment (CI) is still under investigation. The diffusion tensor image (DTI) analysis a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775074/ https://www.ncbi.nlm.nih.gov/pubmed/36552071 http://dx.doi.org/10.3390/brainsci12121611 |
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author | Ke, Zhihong Mo, Yuting Li, Jiangnan Yang, Dan Huang, Lili Yang, Zhiyuan Qin, Ruomeng Mao, Chenglu Lv, Weiping Huang, Yanan Hu, Zheqi Zhang, Bing Xu, Yun |
author_facet | Ke, Zhihong Mo, Yuting Li, Jiangnan Yang, Dan Huang, Lili Yang, Zhiyuan Qin, Ruomeng Mao, Chenglu Lv, Weiping Huang, Yanan Hu, Zheqi Zhang, Bing Xu, Yun |
author_sort | Ke, Zhihong |
collection | PubMed |
description | Glymphatic dysfunction has been linked to cognitive decline in several neurodegenerative diseases. In cerebral small vessel disease (CSVD), the mechanism of white matter hyperintensities (WMH)-related cognitive impairment (CI) is still under investigation. The diffusion tensor image (DTI) analysis along the perivascular space (ALPS) method has been considered to be a reliable parameter to evaluate glymphatic function. Therefore, we applied the ALPS-index to determine the influence of glymphatic function on CI in CSVD. In total, 137 CSVD patients (normal cognitive group, mild CI group, and dementia group) and 52 normal controls were included in this study. The ALPS-index was calculated based on the DTI. Correlation analyses and mediation analysis were conducted to examine the relationship between glymphatic function and cognition. Remarkable differences in the ALPS-index were observed between subjects with and without CI. The ALPS-index was negatively correlated with age, WMH volume, and general cognitive function in all CSVD patients. In the mild CI group, the ALPS-index was independently positively related to episodic memory, and mediated the relationship between WMH volume and episodic memory. In conclusion, the ALPS-index is a potential marker for early recognition of CI in CSVD. Glymphatic dysfunction mediates the relationship between WMH and CI in CSVD. |
format | Online Article Text |
id | pubmed-9775074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97750742022-12-23 Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease Ke, Zhihong Mo, Yuting Li, Jiangnan Yang, Dan Huang, Lili Yang, Zhiyuan Qin, Ruomeng Mao, Chenglu Lv, Weiping Huang, Yanan Hu, Zheqi Zhang, Bing Xu, Yun Brain Sci Article Glymphatic dysfunction has been linked to cognitive decline in several neurodegenerative diseases. In cerebral small vessel disease (CSVD), the mechanism of white matter hyperintensities (WMH)-related cognitive impairment (CI) is still under investigation. The diffusion tensor image (DTI) analysis along the perivascular space (ALPS) method has been considered to be a reliable parameter to evaluate glymphatic function. Therefore, we applied the ALPS-index to determine the influence of glymphatic function on CI in CSVD. In total, 137 CSVD patients (normal cognitive group, mild CI group, and dementia group) and 52 normal controls were included in this study. The ALPS-index was calculated based on the DTI. Correlation analyses and mediation analysis were conducted to examine the relationship between glymphatic function and cognition. Remarkable differences in the ALPS-index were observed between subjects with and without CI. The ALPS-index was negatively correlated with age, WMH volume, and general cognitive function in all CSVD patients. In the mild CI group, the ALPS-index was independently positively related to episodic memory, and mediated the relationship between WMH volume and episodic memory. In conclusion, the ALPS-index is a potential marker for early recognition of CI in CSVD. Glymphatic dysfunction mediates the relationship between WMH and CI in CSVD. MDPI 2022-11-24 /pmc/articles/PMC9775074/ /pubmed/36552071 http://dx.doi.org/10.3390/brainsci12121611 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ke, Zhihong Mo, Yuting Li, Jiangnan Yang, Dan Huang, Lili Yang, Zhiyuan Qin, Ruomeng Mao, Chenglu Lv, Weiping Huang, Yanan Hu, Zheqi Zhang, Bing Xu, Yun Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease |
title | Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease |
title_full | Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease |
title_fullStr | Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease |
title_full_unstemmed | Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease |
title_short | Glymphatic Dysfunction Mediates the Influence of White Matter Hyperintensities on Episodic Memory in Cerebral Small Vessel Disease |
title_sort | glymphatic dysfunction mediates the influence of white matter hyperintensities on episodic memory in cerebral small vessel disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775074/ https://www.ncbi.nlm.nih.gov/pubmed/36552071 http://dx.doi.org/10.3390/brainsci12121611 |
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