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Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment

BACKGROUND: Normal subjects deactivate specific brain regions, notably the posteromedial cortex (PMC), during many tasks. Recent cross-sectional functional magnetic resonance imaging (fMRI) data suggests that deactivation during memory tasks is impaired in Alzheimer's disease (AD). The goal of...

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Autores principales: Petrella, Jeffrey R., Prince, Steven E., Wang, Lihong, Hellegers, Caroline, Doraiswamy, P. Murali
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2040216/
https://www.ncbi.nlm.nih.gov/pubmed/17971867
http://dx.doi.org/10.1371/journal.pone.0001104
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author Petrella, Jeffrey R.
Prince, Steven E.
Wang, Lihong
Hellegers, Caroline
Doraiswamy, P. Murali
author_facet Petrella, Jeffrey R.
Prince, Steven E.
Wang, Lihong
Hellegers, Caroline
Doraiswamy, P. Murali
author_sort Petrella, Jeffrey R.
collection PubMed
description BACKGROUND: Normal subjects deactivate specific brain regions, notably the posteromedial cortex (PMC), during many tasks. Recent cross-sectional functional magnetic resonance imaging (fMRI) data suggests that deactivation during memory tasks is impaired in Alzheimer's disease (AD). The goal of this study was to prospectively determine the prognostic significance of PMC deactivation in mild cognitive impairment (MCI). METHODOLOGY/PRINCIPAL FINDINGS: 75 subjects (34 MCI, 13 AD subjects and 28 controls) underwent baseline fMRI scanning during encoding of novel and familiar face-name pairs. MCI subjects were followed longitudinally to determine conversion to AD. Regression and analysis of covariance models were used to assess the effect of PMC activation/deactivation on conversion to dementia as well as in the longitudinal change in dementia measures. At longitudinal follow up of up to 3.5 years (mean 2.5±0.79 years), 11 MCI subjects converted to AD. The proportion of deactivators was significantly different across all groups: controls (79%), MCI-Nonconverters (73%), MCI-converters (45%), and AD (23%) (p<0.05). Mean PMC activation magnitude parameter estimates, at baseline, were negative in the control (−0.57±0.12) and MCI-Nonconverter (−0.33±0.14) groups, and positive in the MCI-Converter (0.37±0.40) and AD (0.92±0.30) groups. The effect of diagnosis on PMC deactivation remained significant after adjusting for age, education and baseline Mini-Mental State Exam (p<0.05). Baseline PMC activation magnitude was correlated with change in dementia ratings from baseline. CONCLUSION: Loss of physiological functional deactivation in the PMC may have prognostic value in preclinical AD, and could aid in profiling subgroups of MCI subjects at greatest risk for progressive cognitive decline.
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spelling pubmed-20402162007-10-31 Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment Petrella, Jeffrey R. Prince, Steven E. Wang, Lihong Hellegers, Caroline Doraiswamy, P. Murali PLoS One Research Article BACKGROUND: Normal subjects deactivate specific brain regions, notably the posteromedial cortex (PMC), during many tasks. Recent cross-sectional functional magnetic resonance imaging (fMRI) data suggests that deactivation during memory tasks is impaired in Alzheimer's disease (AD). The goal of this study was to prospectively determine the prognostic significance of PMC deactivation in mild cognitive impairment (MCI). METHODOLOGY/PRINCIPAL FINDINGS: 75 subjects (34 MCI, 13 AD subjects and 28 controls) underwent baseline fMRI scanning during encoding of novel and familiar face-name pairs. MCI subjects were followed longitudinally to determine conversion to AD. Regression and analysis of covariance models were used to assess the effect of PMC activation/deactivation on conversion to dementia as well as in the longitudinal change in dementia measures. At longitudinal follow up of up to 3.5 years (mean 2.5±0.79 years), 11 MCI subjects converted to AD. The proportion of deactivators was significantly different across all groups: controls (79%), MCI-Nonconverters (73%), MCI-converters (45%), and AD (23%) (p<0.05). Mean PMC activation magnitude parameter estimates, at baseline, were negative in the control (−0.57±0.12) and MCI-Nonconverter (−0.33±0.14) groups, and positive in the MCI-Converter (0.37±0.40) and AD (0.92±0.30) groups. The effect of diagnosis on PMC deactivation remained significant after adjusting for age, education and baseline Mini-Mental State Exam (p<0.05). Baseline PMC activation magnitude was correlated with change in dementia ratings from baseline. CONCLUSION: Loss of physiological functional deactivation in the PMC may have prognostic value in preclinical AD, and could aid in profiling subgroups of MCI subjects at greatest risk for progressive cognitive decline. Public Library of Science 2007-10-31 /pmc/articles/PMC2040216/ /pubmed/17971867 http://dx.doi.org/10.1371/journal.pone.0001104 Text en Petrella et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Petrella, Jeffrey R.
Prince, Steven E.
Wang, Lihong
Hellegers, Caroline
Doraiswamy, P. Murali
Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment
title Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment
title_full Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment
title_fullStr Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment
title_full_unstemmed Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment
title_short Prognostic Value of Posteromedial Cortex Deactivation in Mild Cognitive Impairment
title_sort prognostic value of posteromedial cortex deactivation in mild cognitive impairment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2040216/
https://www.ncbi.nlm.nih.gov/pubmed/17971867
http://dx.doi.org/10.1371/journal.pone.0001104
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