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Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus

Type 2 diabetes mellitus (T2DM) patients show brain tissue changes in mood and cognitive regulatory sites, but the nature and extent of tissue injury and their associations with symptoms are unclear. Our aim was to examine brain tissue damage in T2DM over controls using mean diffusivity (MD) compute...

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Autores principales: Roy, Bhaswati, Choi, Sarah E, Freeby, Matthew J., Kumar, Rajesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267112/
https://www.ncbi.nlm.nih.gov/pubmed/37316507
http://dx.doi.org/10.1038/s41598-023-35522-9
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author Roy, Bhaswati
Choi, Sarah E
Freeby, Matthew J.
Kumar, Rajesh
author_facet Roy, Bhaswati
Choi, Sarah E
Freeby, Matthew J.
Kumar, Rajesh
author_sort Roy, Bhaswati
collection PubMed
description Type 2 diabetes mellitus (T2DM) patients show brain tissue changes in mood and cognitive regulatory sites, but the nature and extent of tissue injury and their associations with symptoms are unclear. Our aim was to examine brain tissue damage in T2DM over controls using mean diffusivity (MD) computed from diffusion tensor imaging (DTI), and assess correlations with mood and cognitive symptoms in T2DM. We collected DTI series (MRI), mood, and cognitive data, from 169 subjects (68 T2DM and 101 controls). Whole-brain MD-maps were calculated, normalized, smoothed, and compared between groups, as well as correlated with mood and cognition scores in T2DM subjects. Type 2 diabetes patients showed altered cognitive and mood functions over control subjects. Multiple brain sites in T2DM patients showed elevated MD values, indicating chronic tissue changes, including the cerebellum, insula, and frontal and prefrontal cortices, cingulate, and lingual gyrus. Associations between MD values and mood and cognition scores appeared in brain sites mediating these functions. Type 2 diabetes patients show predominantly chronic brain tissue changes in areas mediating mood and cognition functions, and tissue changes from those regions correlate with mood and cognitive symptoms suggesting that the microstructural brain changes may account for the observed functional deficits.
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spelling pubmed-102671122023-06-15 Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus Roy, Bhaswati Choi, Sarah E Freeby, Matthew J. Kumar, Rajesh Sci Rep Article Type 2 diabetes mellitus (T2DM) patients show brain tissue changes in mood and cognitive regulatory sites, but the nature and extent of tissue injury and their associations with symptoms are unclear. Our aim was to examine brain tissue damage in T2DM over controls using mean diffusivity (MD) computed from diffusion tensor imaging (DTI), and assess correlations with mood and cognitive symptoms in T2DM. We collected DTI series (MRI), mood, and cognitive data, from 169 subjects (68 T2DM and 101 controls). Whole-brain MD-maps were calculated, normalized, smoothed, and compared between groups, as well as correlated with mood and cognition scores in T2DM subjects. Type 2 diabetes patients showed altered cognitive and mood functions over control subjects. Multiple brain sites in T2DM patients showed elevated MD values, indicating chronic tissue changes, including the cerebellum, insula, and frontal and prefrontal cortices, cingulate, and lingual gyrus. Associations between MD values and mood and cognition scores appeared in brain sites mediating these functions. Type 2 diabetes patients show predominantly chronic brain tissue changes in areas mediating mood and cognition functions, and tissue changes from those regions correlate with mood and cognitive symptoms suggesting that the microstructural brain changes may account for the observed functional deficits. Nature Publishing Group UK 2023-06-14 /pmc/articles/PMC10267112/ /pubmed/37316507 http://dx.doi.org/10.1038/s41598-023-35522-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Roy, Bhaswati
Choi, Sarah E
Freeby, Matthew J.
Kumar, Rajesh
Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus
title Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus
title_full Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus
title_fullStr Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus
title_full_unstemmed Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus
title_short Microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus
title_sort microstructural brain tissue changes contribute to cognitive and mood deficits in adults with type 2 diabetes mellitus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267112/
https://www.ncbi.nlm.nih.gov/pubmed/37316507
http://dx.doi.org/10.1038/s41598-023-35522-9
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