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Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease

Structural network damage is a potentially important mechanism by which cerebral small vessel disease (SVD) can cause cognitive impairment. As a central hub of the structural network, the role of thalamus in SVD-related cognitive impairments remains unclear. We aimed to determine the associations be...

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Autores principales: Li, Hao, Cai, Mengfei, Jacob, Mina A., Norris, David G., Marques, José P., Chamberland, Maxime, Duering, Marco, Kessels, Roy P.C., de Leeuw, Frank-Erik, Tuladhar, Anil M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121245/
https://www.ncbi.nlm.nih.gov/pubmed/36912138
http://dx.doi.org/10.1161/STROKEAHA.122.041687
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author Li, Hao
Cai, Mengfei
Jacob, Mina A.
Norris, David G.
Marques, José P.
Chamberland, Maxime
Duering, Marco
Kessels, Roy P.C.
de Leeuw, Frank-Erik
Tuladhar, Anil M.
author_facet Li, Hao
Cai, Mengfei
Jacob, Mina A.
Norris, David G.
Marques, José P.
Chamberland, Maxime
Duering, Marco
Kessels, Roy P.C.
de Leeuw, Frank-Erik
Tuladhar, Anil M.
author_sort Li, Hao
collection PubMed
description Structural network damage is a potentially important mechanism by which cerebral small vessel disease (SVD) can cause cognitive impairment. As a central hub of the structural network, the role of thalamus in SVD-related cognitive impairments remains unclear. We aimed to determine the associations between the structural alterations of thalamic subregions and cognitive impairments in SVD. METHODS: In this cross-sectional study, 205 SVD participants without thalamic lacunes from the third follow-up (2020) of the prospective RUN DMC study (Radboud University Nijmegen Diffusion Tensor and Magnetic Resonance Cohort), which was initiated in 2006, Nijmegen, were included. Cognitive functions included processing speed, executive function, and memory. Probabilistic tractography was performed from thalamus to 6 cortical regions, followed by connectivity-based thalamic segmentation to assess each thalamic subregion volume and connectivity (measured by mean diffusivity [MD] of the connecting white matter tracts) with the cortex. Least absolute shrinkage and selection operator regression analysis was conducted to identify the volumes or connectivity of the total thalamus and 6 thalamic subregions that have the strongest association with cognitive performance. Linear regression and mediation analyses were performed to test the association of least absolute shrinkage and selection operator-selected thalamic subregion volume or MD with cognitive performance, while adjusting for age and education. RESULTS: We found that higher MD of the thalamic-motor tract was associated with worse processing speed (β=−0.27; P<0.001), higher MD of the thalamic-frontal tract was associated with worse executive function (β=−0.24; P=0.001), and memory (β=−0.28; P<0.001), respectively. The mediation analysis showed that MD of thalamocortical tracts mediated the association between corresponding thalamic subregion volumes and the cognitive performances in 3 domains. CONCLUSIONS: Our results suggest that the structural alterations of thalamus are linked to cognitive impairment in SVD, largely depending on the damage pattern of the white matter tracts connecting specific thalamic subregions and cortical regions.
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spelling pubmed-101212452023-04-24 Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease Li, Hao Cai, Mengfei Jacob, Mina A. Norris, David G. Marques, José P. Chamberland, Maxime Duering, Marco Kessels, Roy P.C. de Leeuw, Frank-Erik Tuladhar, Anil M. Stroke Original Contributions Structural network damage is a potentially important mechanism by which cerebral small vessel disease (SVD) can cause cognitive impairment. As a central hub of the structural network, the role of thalamus in SVD-related cognitive impairments remains unclear. We aimed to determine the associations between the structural alterations of thalamic subregions and cognitive impairments in SVD. METHODS: In this cross-sectional study, 205 SVD participants without thalamic lacunes from the third follow-up (2020) of the prospective RUN DMC study (Radboud University Nijmegen Diffusion Tensor and Magnetic Resonance Cohort), which was initiated in 2006, Nijmegen, were included. Cognitive functions included processing speed, executive function, and memory. Probabilistic tractography was performed from thalamus to 6 cortical regions, followed by connectivity-based thalamic segmentation to assess each thalamic subregion volume and connectivity (measured by mean diffusivity [MD] of the connecting white matter tracts) with the cortex. Least absolute shrinkage and selection operator regression analysis was conducted to identify the volumes or connectivity of the total thalamus and 6 thalamic subregions that have the strongest association with cognitive performance. Linear regression and mediation analyses were performed to test the association of least absolute shrinkage and selection operator-selected thalamic subregion volume or MD with cognitive performance, while adjusting for age and education. RESULTS: We found that higher MD of the thalamic-motor tract was associated with worse processing speed (β=−0.27; P<0.001), higher MD of the thalamic-frontal tract was associated with worse executive function (β=−0.24; P=0.001), and memory (β=−0.28; P<0.001), respectively. The mediation analysis showed that MD of thalamocortical tracts mediated the association between corresponding thalamic subregion volumes and the cognitive performances in 3 domains. CONCLUSIONS: Our results suggest that the structural alterations of thalamus are linked to cognitive impairment in SVD, largely depending on the damage pattern of the white matter tracts connecting specific thalamic subregions and cortical regions. Lippincott Williams & Wilkins 2023-03-13 2023-05 /pmc/articles/PMC10121245/ /pubmed/36912138 http://dx.doi.org/10.1161/STROKEAHA.122.041687 Text en © 2023 The Authors. https://creativecommons.org/licenses/by-nc-nd/4.0/Stroke is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made. This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.
spellingShingle Original Contributions
Li, Hao
Cai, Mengfei
Jacob, Mina A.
Norris, David G.
Marques, José P.
Chamberland, Maxime
Duering, Marco
Kessels, Roy P.C.
de Leeuw, Frank-Erik
Tuladhar, Anil M.
Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease
title Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease
title_full Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease
title_fullStr Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease
title_full_unstemmed Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease
title_short Dissociable Contributions of Thalamic-Subregions to Cognitive Impairment in Small Vessel Disease
title_sort dissociable contributions of thalamic-subregions to cognitive impairment in small vessel disease
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121245/
https://www.ncbi.nlm.nih.gov/pubmed/36912138
http://dx.doi.org/10.1161/STROKEAHA.122.041687
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