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Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology
BACKGROUND/AIMS: This study examines the longitudinal effect of metabolic syndrome (MetS) on brain-aging indices among cognitively normal (CN) and amnestic mild cognitive impairment (aMCI) groups [single-domain aMCI (saMCI) and multiple-domain aMCI (maMCI)]. METHODS: The study population included 73...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187257/ https://www.ncbi.nlm.nih.gov/pubmed/25337075 http://dx.doi.org/10.1159/000363285 |
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author | Lin, Feng Lo, Raymond Y. Cole, Daniel Ducharme, Simon Chen, Ding-Geng Mapstone, Mark Porsteinsson, Anton |
author_facet | Lin, Feng Lo, Raymond Y. Cole, Daniel Ducharme, Simon Chen, Ding-Geng Mapstone, Mark Porsteinsson, Anton |
author_sort | Lin, Feng |
collection | PubMed |
description | BACKGROUND/AIMS: This study examines the longitudinal effect of metabolic syndrome (MetS) on brain-aging indices among cognitively normal (CN) and amnestic mild cognitive impairment (aMCI) groups [single-domain aMCI (saMCI) and multiple-domain aMCI (maMCI)]. METHODS: The study population included 739 participants (CN = 226, saMCI = 275, and maMCI = 238) from the Alzheimer's Disease Neuroimaging Initiative, a clinic-based, multi-center prospective cohort. Confirmatory factor analysis was employed to determine a MetS latent composite score using baseline data of vascular risk factors. We examined the changes of two Alzheimer's disease (AD) biomarkers, namely [(18)F]fluorodeoxyglucose (FDG)-positron emission tomography (PET) regions of interest and medial temporal lobe volume over 5 years. A cerebrovascular aging index, cerebral white matter (cWM) volume, was examined as a comparison. RESULTS: The vascular risk was similar in all groups. Applying generalized estimating equation modeling, all brain-aging indices declined significantly over time. Higher MetS scores were associated with a faster decline of cWM in the CN and maMCI groups but with a slower decrement of regional glucose metabolism in FDG-PET in the saMCI and maMCI groups. CONCLUSION: At the very early stage of cognitive decline, the vascular burden such as MetS may be in parallel with or independent of AD pathology in contributing to cognitive impairment in terms of accelerating the disclosure of AD pathology. |
format | Online Article Text |
id | pubmed-4187257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-41872572014-10-21 Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology Lin, Feng Lo, Raymond Y. Cole, Daniel Ducharme, Simon Chen, Ding-Geng Mapstone, Mark Porsteinsson, Anton Dement Geriatr Cogn Dis Extra Original Research Article BACKGROUND/AIMS: This study examines the longitudinal effect of metabolic syndrome (MetS) on brain-aging indices among cognitively normal (CN) and amnestic mild cognitive impairment (aMCI) groups [single-domain aMCI (saMCI) and multiple-domain aMCI (maMCI)]. METHODS: The study population included 739 participants (CN = 226, saMCI = 275, and maMCI = 238) from the Alzheimer's Disease Neuroimaging Initiative, a clinic-based, multi-center prospective cohort. Confirmatory factor analysis was employed to determine a MetS latent composite score using baseline data of vascular risk factors. We examined the changes of two Alzheimer's disease (AD) biomarkers, namely [(18)F]fluorodeoxyglucose (FDG)-positron emission tomography (PET) regions of interest and medial temporal lobe volume over 5 years. A cerebrovascular aging index, cerebral white matter (cWM) volume, was examined as a comparison. RESULTS: The vascular risk was similar in all groups. Applying generalized estimating equation modeling, all brain-aging indices declined significantly over time. Higher MetS scores were associated with a faster decline of cWM in the CN and maMCI groups but with a slower decrement of regional glucose metabolism in FDG-PET in the saMCI and maMCI groups. CONCLUSION: At the very early stage of cognitive decline, the vascular burden such as MetS may be in parallel with or independent of AD pathology in contributing to cognitive impairment in terms of accelerating the disclosure of AD pathology. S. Karger AG 2014-06-28 /pmc/articles/PMC4187257/ /pubmed/25337075 http://dx.doi.org/10.1159/000363285 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions. |
spellingShingle | Original Research Article Lin, Feng Lo, Raymond Y. Cole, Daniel Ducharme, Simon Chen, Ding-Geng Mapstone, Mark Porsteinsson, Anton Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology |
title | Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology |
title_full | Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology |
title_fullStr | Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology |
title_full_unstemmed | Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology |
title_short | Longitudinal Effects of Metabolic Syndrome on Alzheimer and Vascular Related Brain Pathology |
title_sort | longitudinal effects of metabolic syndrome on alzheimer and vascular related brain pathology |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4187257/ https://www.ncbi.nlm.nih.gov/pubmed/25337075 http://dx.doi.org/10.1159/000363285 |
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