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Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study
PURPOSE: Subjective cognitive decline (SCD) is the earliest symptom stage of Alzheimer’s disease (AD), and the APOEε4 allele is the strongest genetic risk factor for sporadic AD. Based on graph theory, the resting state functional connectivity (rsFC) in SCD patients with APOEε4 was studied to explor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684393/ https://www.ncbi.nlm.nih.gov/pubmed/34934350 http://dx.doi.org/10.2147/IJGM.S342673 |
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author | Deng, Simin Sun, Lingyu Chen, Weijie Liu, Xiaorong Chen, Shangjie |
author_facet | Deng, Simin Sun, Lingyu Chen, Weijie Liu, Xiaorong Chen, Shangjie |
author_sort | Deng, Simin |
collection | PubMed |
description | PURPOSE: Subjective cognitive decline (SCD) is the earliest symptom stage of Alzheimer’s disease (AD), and the APOEε4 allele is the strongest genetic risk factor for sporadic AD. Based on graph theory, the resting state functional connectivity (rsFC) in SCD patients with APOEε4 was studied to explore the effect of APOEε4 on the rsFC network properties of SCD patients. PATIENTS AND METHODS: This cross-sectional study included MRI image data from 19 SCD patients with APOEε4 (SCD+), 29 SCD patients without APOEε4 (SCD−), and 30 normal control (NC−) individuals without APOEε4. We generated a binary matrix based on anatomical automatic labeling (AAL) 90 atlas to construct the functional network. We then calculated the whole brain network characteristics and intracerebral node characteristics by graph theory. RESULTS: For the whole brain network characteristics, all three groups showed small-worldness. The SCD+ group had increased compensatory information transfer speed and enhanced integration capability. This group also had high heterogeneity for intracerebral node characteristics, mainly in the default mode network, left superior occipital gyrus, and bilateral putamen. CONCLUSION: APOEε4 effects the functional brain network in patients with SCD and may be a potential indicator for the identification of SCD. |
format | Online Article Text |
id | pubmed-8684393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-86843932021-12-20 Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study Deng, Simin Sun, Lingyu Chen, Weijie Liu, Xiaorong Chen, Shangjie Int J Gen Med Original Research PURPOSE: Subjective cognitive decline (SCD) is the earliest symptom stage of Alzheimer’s disease (AD), and the APOEε4 allele is the strongest genetic risk factor for sporadic AD. Based on graph theory, the resting state functional connectivity (rsFC) in SCD patients with APOEε4 was studied to explore the effect of APOEε4 on the rsFC network properties of SCD patients. PATIENTS AND METHODS: This cross-sectional study included MRI image data from 19 SCD patients with APOEε4 (SCD+), 29 SCD patients without APOEε4 (SCD−), and 30 normal control (NC−) individuals without APOEε4. We generated a binary matrix based on anatomical automatic labeling (AAL) 90 atlas to construct the functional network. We then calculated the whole brain network characteristics and intracerebral node characteristics by graph theory. RESULTS: For the whole brain network characteristics, all three groups showed small-worldness. The SCD+ group had increased compensatory information transfer speed and enhanced integration capability. This group also had high heterogeneity for intracerebral node characteristics, mainly in the default mode network, left superior occipital gyrus, and bilateral putamen. CONCLUSION: APOEε4 effects the functional brain network in patients with SCD and may be a potential indicator for the identification of SCD. Dove 2021-12-14 /pmc/articles/PMC8684393/ /pubmed/34934350 http://dx.doi.org/10.2147/IJGM.S342673 Text en © 2021 Deng et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Deng, Simin Sun, Lingyu Chen, Weijie Liu, Xiaorong Chen, Shangjie Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study |
title | Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study |
title_full | Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study |
title_fullStr | Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study |
title_full_unstemmed | Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study |
title_short | Effect of APOEε4 on Functional Brain Network in Patients with Subjective Cognitive Decline: A Resting State Functional MRI Study |
title_sort | effect of apoeε4 on functional brain network in patients with subjective cognitive decline: a resting state functional mri study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684393/ https://www.ncbi.nlm.nih.gov/pubmed/34934350 http://dx.doi.org/10.2147/IJGM.S342673 |
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