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FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type
OBJECTIVES: The logopenic variant of primary progressive aphasia is an atypical clinical variant of Alzheimer’s disease which is typically characterized by left temporoparietal atrophy on magnetic resonance imaging and hypometabolism on F-18 fluorodeoxyglucose positron emission tomography. We aimed...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633885/ https://www.ncbi.nlm.nih.gov/pubmed/23626825 http://dx.doi.org/10.1371/journal.pone.0062471 |
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author | Madhavan, Ajay Whitwell, Jennifer L. Weigand, Stephen D. Duffy, Joseph R. Strand, Edythe A. Machulda, Mary M. Tosakulwong, Nirubol Senjem, Matthew L. Gunter, Jeffrey L. Lowe, Val J. Petersen, Ronald C. Jack, Clifford R. Josephs, Keith A. |
author_facet | Madhavan, Ajay Whitwell, Jennifer L. Weigand, Stephen D. Duffy, Joseph R. Strand, Edythe A. Machulda, Mary M. Tosakulwong, Nirubol Senjem, Matthew L. Gunter, Jeffrey L. Lowe, Val J. Petersen, Ronald C. Jack, Clifford R. Josephs, Keith A. |
author_sort | Madhavan, Ajay |
collection | PubMed |
description | OBJECTIVES: The logopenic variant of primary progressive aphasia is an atypical clinical variant of Alzheimer’s disease which is typically characterized by left temporoparietal atrophy on magnetic resonance imaging and hypometabolism on F-18 fluorodeoxyglucose positron emission tomography. We aimed to characterize and compare patterns of atrophy and hypometabolism in logopenic primary progressive aphasia, and determine which brain regions and imaging modality best differentiates logopenic primary progressive aphasia from typical dementia of the Alzheimer’s type. METHODS: A total of 27 logopenic primary progressive aphasia subjects underwent fluorodeoxyglucose positron emission tomography and volumetric magnetic resonance imaging. These subjects were matched to 27 controls and 27 subjects with dementia of the Alzheimer’s type. Patterns of atrophy and hypometabolism were assessed at the voxel and region-level using Statistical Parametric Mapping. Penalized logistic regression analysis was used to determine what combinations of regions best discriminate between groups. RESULTS: Atrophy and hypometabolism was observed in lateral temporoparietal and medial parietal lobes, left greater than right, and left frontal lobe in the logopenic group. The logopenic group showed greater left inferior, middle and superior lateral temporal atrophy (inferior p = 0.02; middle p = 0.007, superior p = 0.002) and hypometabolism (inferior p = 0.006, middle p = 0.002, superior p = 0.001), and less right medial temporal atrophy (p = 0.02) and hypometabolism (p<0.001), and right posterior cingulate hypometabolism (p<0.001) than dementia of the Alzheimer’s type. An age-adjusted penalized logistic model incorporating atrophy and hypometabolism achieved excellent discrimination (area under the receiver operator characteristic curve = 0.89) between logopenic and dementia of the Alzheimer’s type subjects, with optimal discrimination achieved using right medial temporal and posterior cingulate hypometabolism, left inferior, middle and superior temporal hypometabolism, and left superior temporal volume. CONCLUSIONS: Patterns of atrophy and hypometabolism both differ between logopenic primary progressive aphasia and dementia of the Alzheimer’s type and both modalities provide excellent discrimination between groups. |
format | Online Article Text |
id | pubmed-3633885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36338852013-04-26 FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type Madhavan, Ajay Whitwell, Jennifer L. Weigand, Stephen D. Duffy, Joseph R. Strand, Edythe A. Machulda, Mary M. Tosakulwong, Nirubol Senjem, Matthew L. Gunter, Jeffrey L. Lowe, Val J. Petersen, Ronald C. Jack, Clifford R. Josephs, Keith A. PLoS One Research Article OBJECTIVES: The logopenic variant of primary progressive aphasia is an atypical clinical variant of Alzheimer’s disease which is typically characterized by left temporoparietal atrophy on magnetic resonance imaging and hypometabolism on F-18 fluorodeoxyglucose positron emission tomography. We aimed to characterize and compare patterns of atrophy and hypometabolism in logopenic primary progressive aphasia, and determine which brain regions and imaging modality best differentiates logopenic primary progressive aphasia from typical dementia of the Alzheimer’s type. METHODS: A total of 27 logopenic primary progressive aphasia subjects underwent fluorodeoxyglucose positron emission tomography and volumetric magnetic resonance imaging. These subjects were matched to 27 controls and 27 subjects with dementia of the Alzheimer’s type. Patterns of atrophy and hypometabolism were assessed at the voxel and region-level using Statistical Parametric Mapping. Penalized logistic regression analysis was used to determine what combinations of regions best discriminate between groups. RESULTS: Atrophy and hypometabolism was observed in lateral temporoparietal and medial parietal lobes, left greater than right, and left frontal lobe in the logopenic group. The logopenic group showed greater left inferior, middle and superior lateral temporal atrophy (inferior p = 0.02; middle p = 0.007, superior p = 0.002) and hypometabolism (inferior p = 0.006, middle p = 0.002, superior p = 0.001), and less right medial temporal atrophy (p = 0.02) and hypometabolism (p<0.001), and right posterior cingulate hypometabolism (p<0.001) than dementia of the Alzheimer’s type. An age-adjusted penalized logistic model incorporating atrophy and hypometabolism achieved excellent discrimination (area under the receiver operator characteristic curve = 0.89) between logopenic and dementia of the Alzheimer’s type subjects, with optimal discrimination achieved using right medial temporal and posterior cingulate hypometabolism, left inferior, middle and superior temporal hypometabolism, and left superior temporal volume. CONCLUSIONS: Patterns of atrophy and hypometabolism both differ between logopenic primary progressive aphasia and dementia of the Alzheimer’s type and both modalities provide excellent discrimination between groups. Public Library of Science 2013-04-23 /pmc/articles/PMC3633885/ /pubmed/23626825 http://dx.doi.org/10.1371/journal.pone.0062471 Text en © 2013 Madhavan 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 Madhavan, Ajay Whitwell, Jennifer L. Weigand, Stephen D. Duffy, Joseph R. Strand, Edythe A. Machulda, Mary M. Tosakulwong, Nirubol Senjem, Matthew L. Gunter, Jeffrey L. Lowe, Val J. Petersen, Ronald C. Jack, Clifford R. Josephs, Keith A. FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type |
title | FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type |
title_full | FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type |
title_fullStr | FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type |
title_full_unstemmed | FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type |
title_short | FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type |
title_sort | fdg pet and mri in logopenic primary progressive aphasia versus dementia of the alzheimer’s type |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633885/ https://www.ncbi.nlm.nih.gov/pubmed/23626825 http://dx.doi.org/10.1371/journal.pone.0062471 |
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