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Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease

INTRODUCTION: Cerebral small-vessel disease (SVD) represents the most frequent type of vascular brain lesions, often coexisting with Alzheimer disease (AD). By quantifying white matter hyperintensities (WMH) and hippocampal and parietal atrophy, we aimed to describe the prevalence and severity of SV...

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Autores principales: Mimenza-Alvarado, Alberto, Aguilar-Navarro, Sara G., Yeverino-Castro, Sara, Mendoza-Franco, César, Ávila-Funes, José Alberto, Román, Gustavo C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006607/
https://www.ncbi.nlm.nih.gov/pubmed/29928288
http://dx.doi.org/10.1159/000488705
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author Mimenza-Alvarado, Alberto
Aguilar-Navarro, Sara G.
Yeverino-Castro, Sara
Mendoza-Franco, César
Ávila-Funes, José Alberto
Román, Gustavo C.
author_facet Mimenza-Alvarado, Alberto
Aguilar-Navarro, Sara G.
Yeverino-Castro, Sara
Mendoza-Franco, César
Ávila-Funes, José Alberto
Román, Gustavo C.
author_sort Mimenza-Alvarado, Alberto
collection PubMed
description INTRODUCTION: Cerebral small-vessel disease (SVD) represents the most frequent type of vascular brain lesions, often coexisting with Alzheimer disease (AD). By quantifying white matter hyperintensities (WMH) and hippocampal and parietal atrophy, we aimed to describe the prevalence and severity of SVD among older adults with normal cognition (NC), mild cognitive impairment (MCI), and probable AD and to describe associated risk factors. METHODS: This study included 105 older adults evaluated with magnetic resonance imaging and clinical and neuropsychological tests. We used the Fazekas scale (FS) for quantification of WMH, the Scheltens scale (SS) for hippocampal atrophy, and the Koedam scale (KS) for parietal atrophy. Logistic regression models were performed to determine the association between FS, SS, and KS scores and the presence of NC, MCI, or probable AD. RESULTS: Compared to NC subjects, SVD was more prevalent in MCI and probable AD subjects. After adjusting for confounding factors, logistic regression showed a positive association between higher scores on the FS and probable AD (OR = 7.6, 95% CI 2.7–20, p < 0.001). With the use of the SS and KS (OR = 4.5, 95% CI 3.5–58, p = 0.003 and OR = 8.9, 95% CI 1–72, p = 0.04, respectively), the risk also remained significant for probable AD. CONCLUSIONS: These results suggest an association between severity of vascular brain lesions and neurodegeneration.
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spelling pubmed-60066072018-06-20 Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease Mimenza-Alvarado, Alberto Aguilar-Navarro, Sara G. Yeverino-Castro, Sara Mendoza-Franco, César Ávila-Funes, José Alberto Román, Gustavo C. Dement Geriatr Cogn Dis Extra Original Research Article INTRODUCTION: Cerebral small-vessel disease (SVD) represents the most frequent type of vascular brain lesions, often coexisting with Alzheimer disease (AD). By quantifying white matter hyperintensities (WMH) and hippocampal and parietal atrophy, we aimed to describe the prevalence and severity of SVD among older adults with normal cognition (NC), mild cognitive impairment (MCI), and probable AD and to describe associated risk factors. METHODS: This study included 105 older adults evaluated with magnetic resonance imaging and clinical and neuropsychological tests. We used the Fazekas scale (FS) for quantification of WMH, the Scheltens scale (SS) for hippocampal atrophy, and the Koedam scale (KS) for parietal atrophy. Logistic regression models were performed to determine the association between FS, SS, and KS scores and the presence of NC, MCI, or probable AD. RESULTS: Compared to NC subjects, SVD was more prevalent in MCI and probable AD subjects. After adjusting for confounding factors, logistic regression showed a positive association between higher scores on the FS and probable AD (OR = 7.6, 95% CI 2.7–20, p < 0.001). With the use of the SS and KS (OR = 4.5, 95% CI 3.5–58, p = 0.003 and OR = 8.9, 95% CI 1–72, p = 0.04, respectively), the risk also remained significant for probable AD. CONCLUSIONS: These results suggest an association between severity of vascular brain lesions and neurodegeneration. S. Karger AG 2018-05-16 /pmc/articles/PMC6006607/ /pubmed/29928288 http://dx.doi.org/10.1159/000488705 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes as well as any distribution of modified material requires written permission.
spellingShingle Original Research Article
Mimenza-Alvarado, Alberto
Aguilar-Navarro, Sara G.
Yeverino-Castro, Sara
Mendoza-Franco, César
Ávila-Funes, José Alberto
Román, Gustavo C.
Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease
title Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease
title_full Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease
title_fullStr Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease
title_full_unstemmed Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease
title_short Neuroimaging Characteristics of Small-Vessel Disease in Older Adults with Normal Cognition, Mild Cognitive Impairment, and Alzheimer Disease
title_sort neuroimaging characteristics of small-vessel disease in older adults with normal cognition, mild cognitive impairment, and alzheimer disease
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006607/
https://www.ncbi.nlm.nih.gov/pubmed/29928288
http://dx.doi.org/10.1159/000488705
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