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(18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies

Among individuals with dementia with Lewy bodies, pathologic correlates of clinical course include the presence and extent of coexisting Alzheimer’s pathology and the presence of transitional or diffuse Lewy body disease. The objectives of this study are to determine (i) whether (18)F-fluorodeoxyglu...

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Autores principales: Graff-Radford, Jonathan, Lesnick, Timothy G, Savica, Rodolfo, Chen, Qin, Ferman, Tanis J, Przybelski, Scott A, Jones, David T, Senjem, Matthew L, Gunter, Jeffrey L, Kremers, Walter K, Jack, Clifford R, Lowe, Val J, Petersen, Ronald C, Knopman, David S, Boeve, Bradley F, Murray, Melissa E, Dickson, Dennis W, Kantarci, Kejal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293797/
https://www.ncbi.nlm.nih.gov/pubmed/32566926
http://dx.doi.org/10.1093/braincomms/fcaa040
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author Graff-Radford, Jonathan
Lesnick, Timothy G
Savica, Rodolfo
Chen, Qin
Ferman, Tanis J
Przybelski, Scott A
Jones, David T
Senjem, Matthew L
Gunter, Jeffrey L
Kremers, Walter K
Jack, Clifford R
Lowe, Val J
Petersen, Ronald C
Knopman, David S
Boeve, Bradley F
Murray, Melissa E
Dickson, Dennis W
Kantarci, Kejal
author_facet Graff-Radford, Jonathan
Lesnick, Timothy G
Savica, Rodolfo
Chen, Qin
Ferman, Tanis J
Przybelski, Scott A
Jones, David T
Senjem, Matthew L
Gunter, Jeffrey L
Kremers, Walter K
Jack, Clifford R
Lowe, Val J
Petersen, Ronald C
Knopman, David S
Boeve, Bradley F
Murray, Melissa E
Dickson, Dennis W
Kantarci, Kejal
author_sort Graff-Radford, Jonathan
collection PubMed
description Among individuals with dementia with Lewy bodies, pathologic correlates of clinical course include the presence and extent of coexisting Alzheimer’s pathology and the presence of transitional or diffuse Lewy body disease. The objectives of this study are to determine (i) whether (18)F-fluorodeoxyglucose PET signature patterns of dementia with Lewy bodies are associated with the extent of coexisting Alzheimer’s pathology and the presence of transitional or diffuse Lewy body disease and (ii) whether these (18)F-fluorodeoxyglucose pattern(s) are associated with clinical course in dementia with Lewy bodies. Two groups of participants were included: a pathology-confirmed subset with Lewy body disease (n = 34) and a clinically diagnosed group of dementia with Lewy bodies (n = 87). A subset of the clinically diagnosed group was followed longitudinally (n = 51). We evaluated whether (18)F-fluorodeoxyglucose PET features of dementia with Lewy bodies (higher cingulate island sign ratio and greater occipital hypometabolism) varied by Lewy body disease subtype (transitional versus diffuse) and Braak neurofibrillary tangle stage. We investigated whether the PET features were associated with the clinical trajectories by performing regression models predicting Clinical Dementia Rating Scale Sum of Boxes. Among autopsied participants, there was no difference in cingulate island sign or occipital hypometabolism by Lewy body disease type, but those with a lower Braak tangle stage had a higher cingulate island sign ratio compared to those with a higher Braak tangle stage. Among the clinically diagnosed dementia with Lewy bodies participants, a higher cingulate island ratio was associated with better cognitive scores at baseline and longitudinally. A higher (18)F-fluorodeoxyglucose PET cingulate island sign ratio was associated with lower Braak tangle stage at autopsy, predicted a better clinical trajectory in dementia with Lewy body patients and may allow for improved prognostication of the clinical course in this disease.
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spelling pubmed-72937972020-06-17 (18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies Graff-Radford, Jonathan Lesnick, Timothy G Savica, Rodolfo Chen, Qin Ferman, Tanis J Przybelski, Scott A Jones, David T Senjem, Matthew L Gunter, Jeffrey L Kremers, Walter K Jack, Clifford R Lowe, Val J Petersen, Ronald C Knopman, David S Boeve, Bradley F Murray, Melissa E Dickson, Dennis W Kantarci, Kejal Brain Commun Original Article Among individuals with dementia with Lewy bodies, pathologic correlates of clinical course include the presence and extent of coexisting Alzheimer’s pathology and the presence of transitional or diffuse Lewy body disease. The objectives of this study are to determine (i) whether (18)F-fluorodeoxyglucose PET signature patterns of dementia with Lewy bodies are associated with the extent of coexisting Alzheimer’s pathology and the presence of transitional or diffuse Lewy body disease and (ii) whether these (18)F-fluorodeoxyglucose pattern(s) are associated with clinical course in dementia with Lewy bodies. Two groups of participants were included: a pathology-confirmed subset with Lewy body disease (n = 34) and a clinically diagnosed group of dementia with Lewy bodies (n = 87). A subset of the clinically diagnosed group was followed longitudinally (n = 51). We evaluated whether (18)F-fluorodeoxyglucose PET features of dementia with Lewy bodies (higher cingulate island sign ratio and greater occipital hypometabolism) varied by Lewy body disease subtype (transitional versus diffuse) and Braak neurofibrillary tangle stage. We investigated whether the PET features were associated with the clinical trajectories by performing regression models predicting Clinical Dementia Rating Scale Sum of Boxes. Among autopsied participants, there was no difference in cingulate island sign or occipital hypometabolism by Lewy body disease type, but those with a lower Braak tangle stage had a higher cingulate island sign ratio compared to those with a higher Braak tangle stage. Among the clinically diagnosed dementia with Lewy bodies participants, a higher cingulate island ratio was associated with better cognitive scores at baseline and longitudinally. A higher (18)F-fluorodeoxyglucose PET cingulate island sign ratio was associated with lower Braak tangle stage at autopsy, predicted a better clinical trajectory in dementia with Lewy body patients and may allow for improved prognostication of the clinical course in this disease. Oxford University Press 2020-04-08 /pmc/articles/PMC7293797/ /pubmed/32566926 http://dx.doi.org/10.1093/braincomms/fcaa040 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Graff-Radford, Jonathan
Lesnick, Timothy G
Savica, Rodolfo
Chen, Qin
Ferman, Tanis J
Przybelski, Scott A
Jones, David T
Senjem, Matthew L
Gunter, Jeffrey L
Kremers, Walter K
Jack, Clifford R
Lowe, Val J
Petersen, Ronald C
Knopman, David S
Boeve, Bradley F
Murray, Melissa E
Dickson, Dennis W
Kantarci, Kejal
(18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies
title (18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies
title_full (18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies
title_fullStr (18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies
title_full_unstemmed (18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies
title_short (18)F-fluorodeoxyglucose positron emission tomography in dementia with Lewy bodies
title_sort (18)f-fluorodeoxyglucose positron emission tomography in dementia with lewy bodies
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293797/
https://www.ncbi.nlm.nih.gov/pubmed/32566926
http://dx.doi.org/10.1093/braincomms/fcaa040
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