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Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement
The disruption of functional connectivity is one of the early events that occurs in the brains of Alzheimer’s disease (AD) patients. This paper reports a study on the clustering structure of functional connectivity in eight important brain networks in healthy, AD, and prodromal stage subjects. We us...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572464/ https://www.ncbi.nlm.nih.gov/pubmed/37835817 http://dx.doi.org/10.3390/diagnostics13193074 |
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author | Lama, Ramesh Kumar Kwon, Goo-Rak |
author_facet | Lama, Ramesh Kumar Kwon, Goo-Rak |
author_sort | Lama, Ramesh Kumar |
collection | PubMed |
description | The disruption of functional connectivity is one of the early events that occurs in the brains of Alzheimer’s disease (AD) patients. This paper reports a study on the clustering structure of functional connectivity in eight important brain networks in healthy, AD, and prodromal stage subjects. We used the threshold-free cluster enhancement (TFCE) method to explore the connectivity from resting-state functional MR images (rs-fMRIs). We conducted the study on a total of 32 AD, 32 HC, and 31 MCI subjects. We modeled the brain as a graph-based network to study these impairments, and pairwise Pearson’s correlation-based functional connectivity was used to construct the brain network. The study found that connections in the sensory motor network (SMN), dorsal attention network (DAN), salience network (SAN), default mode network (DMN), and cerebral network were severely affected in AD and MCI. The disruption in these networks may serve as potential biomarkers for distinguishing AD and MCI from HC. The study suggests that alterations in functional connectivity in these networks may contribute to cognitive deficits observed in AD and MCI. Additionally, a negative correlation was observed between the global clinical dementia rating (CDR) score and the Z-score of functional connectivity within identified clusters in AD subjects. These findings provide compelling evidence suggesting that the neurodegenerative disruption of functional magnetic resonance imaging (fMRI) connectivity is extensively distributed across multiple networks in individuals diagnosed with AD. |
format | Online Article Text |
id | pubmed-10572464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105724642023-10-14 Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement Lama, Ramesh Kumar Kwon, Goo-Rak Diagnostics (Basel) Article The disruption of functional connectivity is one of the early events that occurs in the brains of Alzheimer’s disease (AD) patients. This paper reports a study on the clustering structure of functional connectivity in eight important brain networks in healthy, AD, and prodromal stage subjects. We used the threshold-free cluster enhancement (TFCE) method to explore the connectivity from resting-state functional MR images (rs-fMRIs). We conducted the study on a total of 32 AD, 32 HC, and 31 MCI subjects. We modeled the brain as a graph-based network to study these impairments, and pairwise Pearson’s correlation-based functional connectivity was used to construct the brain network. The study found that connections in the sensory motor network (SMN), dorsal attention network (DAN), salience network (SAN), default mode network (DMN), and cerebral network were severely affected in AD and MCI. The disruption in these networks may serve as potential biomarkers for distinguishing AD and MCI from HC. The study suggests that alterations in functional connectivity in these networks may contribute to cognitive deficits observed in AD and MCI. Additionally, a negative correlation was observed between the global clinical dementia rating (CDR) score and the Z-score of functional connectivity within identified clusters in AD subjects. These findings provide compelling evidence suggesting that the neurodegenerative disruption of functional magnetic resonance imaging (fMRI) connectivity is extensively distributed across multiple networks in individuals diagnosed with AD. MDPI 2023-09-28 /pmc/articles/PMC10572464/ /pubmed/37835817 http://dx.doi.org/10.3390/diagnostics13193074 Text en © 2023 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 Lama, Ramesh Kumar Kwon, Goo-Rak Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement |
title | Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement |
title_full | Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement |
title_fullStr | Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement |
title_full_unstemmed | Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement |
title_short | Resting-State Functional Connectivity Difference in Alzheimer’s Disease and Mild Cognitive Impairment Using Threshold-Free Cluster Enhancement |
title_sort | resting-state functional connectivity difference in alzheimer’s disease and mild cognitive impairment using threshold-free cluster enhancement |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572464/ https://www.ncbi.nlm.nih.gov/pubmed/37835817 http://dx.doi.org/10.3390/diagnostics13193074 |
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