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Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study
BACKGROUND: The ε4 allele of the apolipoprotein E (APOE) gene is a strong genetic risk factor for aging-related cognitive decline. However, the causal connection between ε4 alleles and cognition is not well understood. The objective of this study was to identify the roles of cerebral blood flow (CBF...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279129/ https://www.ncbi.nlm.nih.gov/pubmed/35847686 http://dx.doi.org/10.3389/fnagi.2022.928925 |
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author | Wang, Yan-Li Sun, Mengfan Wang, Fang-Ze Wang, Xiaohong Jia, Ziyan Zhang, Yuan Li, Runzhi Jiang, Jiwei Wang, Linlin Li, Wenyi Sun, Yongan Chen, Jinglong Zhang, Cuicui Shi, Baolin Liu, Jianjian Liu, Xiangrong Xu, Jun |
author_facet | Wang, Yan-Li Sun, Mengfan Wang, Fang-Ze Wang, Xiaohong Jia, Ziyan Zhang, Yuan Li, Runzhi Jiang, Jiwei Wang, Linlin Li, Wenyi Sun, Yongan Chen, Jinglong Zhang, Cuicui Shi, Baolin Liu, Jianjian Liu, Xiangrong Xu, Jun |
author_sort | Wang, Yan-Li |
collection | PubMed |
description | BACKGROUND: The ε4 allele of the apolipoprotein E (APOE) gene is a strong genetic risk factor for aging-related cognitive decline. However, the causal connection between ε4 alleles and cognition is not well understood. The objective of this study was to identify the roles of cerebral blood flow (CBF) in cognitive-related brain areas in mediating the associations of APOE with cognition. METHODS: The multiple linear regression analyses were conducted on 369 subjects (mean age of 68.8 years; 62.9% of women; 29.3% of APOE ε4 allele carriers). Causal mediation analyses with 5,000 bootstrapped iterations were conducted to explore the mediation effects. RESULT: APOE ε4 allele was negatively associated with cognition (P < 0.05) and CBF in the amygdala, hippocampus, middle temporal gyrus, posterior cingulate, and precuneus (all P < 0.05). The effect of the APOE genotype on cognition was partly mediated by the above CBF (all P < 0.05). CONCLUSION: CBF partially mediates the potential links between APOE genotype and cognition. Overall, the APOE ε4 allele may lead to a dysregulation of the vascular structure and function with reduced cerebral perfusion, which in turn leads to cognitive impairment. |
format | Online Article Text |
id | pubmed-9279129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92791292022-07-15 Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study Wang, Yan-Li Sun, Mengfan Wang, Fang-Ze Wang, Xiaohong Jia, Ziyan Zhang, Yuan Li, Runzhi Jiang, Jiwei Wang, Linlin Li, Wenyi Sun, Yongan Chen, Jinglong Zhang, Cuicui Shi, Baolin Liu, Jianjian Liu, Xiangrong Xu, Jun Front Aging Neurosci Neuroscience BACKGROUND: The ε4 allele of the apolipoprotein E (APOE) gene is a strong genetic risk factor for aging-related cognitive decline. However, the causal connection between ε4 alleles and cognition is not well understood. The objective of this study was to identify the roles of cerebral blood flow (CBF) in cognitive-related brain areas in mediating the associations of APOE with cognition. METHODS: The multiple linear regression analyses were conducted on 369 subjects (mean age of 68.8 years; 62.9% of women; 29.3% of APOE ε4 allele carriers). Causal mediation analyses with 5,000 bootstrapped iterations were conducted to explore the mediation effects. RESULT: APOE ε4 allele was negatively associated with cognition (P < 0.05) and CBF in the amygdala, hippocampus, middle temporal gyrus, posterior cingulate, and precuneus (all P < 0.05). The effect of the APOE genotype on cognition was partly mediated by the above CBF (all P < 0.05). CONCLUSION: CBF partially mediates the potential links between APOE genotype and cognition. Overall, the APOE ε4 allele may lead to a dysregulation of the vascular structure and function with reduced cerebral perfusion, which in turn leads to cognitive impairment. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9279129/ /pubmed/35847686 http://dx.doi.org/10.3389/fnagi.2022.928925 Text en Copyright © 2022 Wang, Sun, Wang, Wang, Jia, Zhang, Li, Jiang, Wang, Li, Sun, Chen, Zhang, Shi, Liu, Liu and Xu. 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 Wang, Yan-Li Sun, Mengfan Wang, Fang-Ze Wang, Xiaohong Jia, Ziyan Zhang, Yuan Li, Runzhi Jiang, Jiwei Wang, Linlin Li, Wenyi Sun, Yongan Chen, Jinglong Zhang, Cuicui Shi, Baolin Liu, Jianjian Liu, Xiangrong Xu, Jun Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study |
title | Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study |
title_full | Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study |
title_fullStr | Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study |
title_full_unstemmed | Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study |
title_short | Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study |
title_sort | mediation of the apoe associations with cognition through cerebral blood flow: the cibl study |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279129/ https://www.ncbi.nlm.nih.gov/pubmed/35847686 http://dx.doi.org/10.3389/fnagi.2022.928925 |
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