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Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease

Disruptions in brain connectivity have been widely reported in Alzheimer’s disease (AD). Morphometric similarity (MS) mapping provides a new way of estimating structural connectivity by interregional correlation of T1WI- and DTI-derived parameters within individual brains. Here, we aimed to identify...

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Autores principales: Zhang, Yang, Ma, Min, Xie, Zhonghua, Wu, Heng, Zhang, Nan, Shen, Junlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522649/
https://www.ncbi.nlm.nih.gov/pubmed/34671240
http://dx.doi.org/10.3389/fnins.2021.731292
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author Zhang, Yang
Ma, Min
Xie, Zhonghua
Wu, Heng
Zhang, Nan
Shen, Junlin
author_facet Zhang, Yang
Ma, Min
Xie, Zhonghua
Wu, Heng
Zhang, Nan
Shen, Junlin
author_sort Zhang, Yang
collection PubMed
description Disruptions in brain connectivity have been widely reported in Alzheimer’s disease (AD). Morphometric similarity (MS) mapping provides a new way of estimating structural connectivity by interregional correlation of T1WI- and DTI-derived parameters within individual brains. Here, we aimed to identify AD-related MS changing patterns and genes related to the changes and further explored the molecular and cellular mechanism underlying MS changes in AD. Both 3D-T1WI and DTI data of 106 AD patients and 106 well-matched healthy elderly individuals from the ADNI database were included in our study. Cortical regions with significantly decreased MS were found in the temporal and parietal cortex, increased MS was found in the frontal cortex and variant changes were found in the occipital cortex in AD patients. Mean MS in regions with significantly changed MS was positively or negatively associated with memory function. Negative MS-related genes were significantly downregulated in AD, specifically enriched in neurons, and participated in biological processes, with the most significant term being synaptic transmission. This study revealed AD-related cortical MS changes associated with memory function. Linking gene expression to cortical MS changes may provide a possible molecular and cellular substrate for MS abnormality and cognitive decline in AD.
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spelling pubmed-85226492021-10-19 Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease Zhang, Yang Ma, Min Xie, Zhonghua Wu, Heng Zhang, Nan Shen, Junlin Front Neurosci Neuroscience Disruptions in brain connectivity have been widely reported in Alzheimer’s disease (AD). Morphometric similarity (MS) mapping provides a new way of estimating structural connectivity by interregional correlation of T1WI- and DTI-derived parameters within individual brains. Here, we aimed to identify AD-related MS changing patterns and genes related to the changes and further explored the molecular and cellular mechanism underlying MS changes in AD. Both 3D-T1WI and DTI data of 106 AD patients and 106 well-matched healthy elderly individuals from the ADNI database were included in our study. Cortical regions with significantly decreased MS were found in the temporal and parietal cortex, increased MS was found in the frontal cortex and variant changes were found in the occipital cortex in AD patients. Mean MS in regions with significantly changed MS was positively or negatively associated with memory function. Negative MS-related genes were significantly downregulated in AD, specifically enriched in neurons, and participated in biological processes, with the most significant term being synaptic transmission. This study revealed AD-related cortical MS changes associated with memory function. Linking gene expression to cortical MS changes may provide a possible molecular and cellular substrate for MS abnormality and cognitive decline in AD. Frontiers Media S.A. 2021-09-29 /pmc/articles/PMC8522649/ /pubmed/34671240 http://dx.doi.org/10.3389/fnins.2021.731292 Text en Copyright © 2021 Zhang, Ma, Xie, Wu, Zhang and Shen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Zhang, Yang
Ma, Min
Xie, Zhonghua
Wu, Heng
Zhang, Nan
Shen, Junlin
Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease
title Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease
title_full Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease
title_fullStr Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease
title_full_unstemmed Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease
title_short Bridging the Gap Between Morphometric Similarity Mapping and Gene Transcription in Alzheimer’s Disease
title_sort bridging the gap between morphometric similarity mapping and gene transcription in alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522649/
https://www.ncbi.nlm.nih.gov/pubmed/34671240
http://dx.doi.org/10.3389/fnins.2021.731292
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