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FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD

BACKGROUND AND PURPOSE: Patients with dementia with Lewy bodies (DLB) are characterized by hypometabolism in the parieto–occipital cortex and the cingulate island sign (CIS) on (18)F-fluorodeoxyglucose (FDG) PET. Whether this pattern of hypometabolism is present as early as the prodromal stage of DL...

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Autores principales: Kantarci, Kejal, Boeve, Bradley F., Przybelski, Scott A., Lesnick, Timothy G., Chen, Qin, Fields, Julie, Schwarz, Christopher G., Senjem, Matthew L., Gunte, Jeffrey L., Jack, Clifford R., Min, Paul, Jain, Manoj, Migayawa, Toji, Savica, Rodolfo, Graff-Radford, Jonathan, Botha, Hugo, Jones, David T., Knopman, David S., Graff-Radford, Neill, Ferman, Tanis J., Petersen, Ronald C., Lowe, Val J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278422/
https://www.ncbi.nlm.nih.gov/pubmed/34252877
http://dx.doi.org/10.1016/j.nicl.2021.102754
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author Kantarci, Kejal
Boeve, Bradley F.
Przybelski, Scott A.
Lesnick, Timothy G.
Chen, Qin
Fields, Julie
Schwarz, Christopher G.
Senjem, Matthew L.
Gunte, Jeffrey L.
Jack, Clifford R.
Min, Paul
Jain, Manoj
Migayawa, Toji
Savica, Rodolfo
Graff-Radford, Jonathan
Botha, Hugo
Jones, David T.
Knopman, David S.
Graff-Radford, Neill
Ferman, Tanis J.
Petersen, Ronald C.
Lowe, Val J.
author_facet Kantarci, Kejal
Boeve, Bradley F.
Przybelski, Scott A.
Lesnick, Timothy G.
Chen, Qin
Fields, Julie
Schwarz, Christopher G.
Senjem, Matthew L.
Gunte, Jeffrey L.
Jack, Clifford R.
Min, Paul
Jain, Manoj
Migayawa, Toji
Savica, Rodolfo
Graff-Radford, Jonathan
Botha, Hugo
Jones, David T.
Knopman, David S.
Graff-Radford, Neill
Ferman, Tanis J.
Petersen, Ronald C.
Lowe, Val J.
author_sort Kantarci, Kejal
collection PubMed
description BACKGROUND AND PURPOSE: Patients with dementia with Lewy bodies (DLB) are characterized by hypometabolism in the parieto–occipital cortex and the cingulate island sign (CIS) on (18)F-fluorodeoxyglucose (FDG) PET. Whether this pattern of hypometabolism is present as early as the prodromal stage of DLB is unknown. We investigated the pattern of hypometabolism in patients with mild cognitive impairment (MCI) who progressed to probable DLB compared to MCI patients who progressed to Alzheimer’s disease (AD) dementia and clinically unimpaired (CU) controls. METHODS: Patients with MCI from the Mayo Clinic Alzheimer’s Disease Research Center who underwent FDG PET at baseline and progressed to either probable DLB (MCI-DLB; n = 17) or AD dementia (MCI-AD; n = 41) during follow-up, and a comparison cohort of CU controls (n = 100) were included. RESULTS: Patients with MCI-DLB had hypometabolism in the parieto-occipital cortex extending into temporal lobes, substantia nigra and thalamus. When compared to MCI-AD, medial temporal and posterior cingulate metabolism were preserved in patients with MCI-DLB, accompanied by greater hypometabolism in the substantia nigra in MCI-DLB compared to MCI-AD. In distinguishing MCI-DLB from MCI-AD at the maximum value of Youden’s index, CIS ratio was highly specific (90%) but not sensitive (59%), but a higher medial temporal to substantia nigra ratio was both sensitive (94%) and specific (83%). CONCLUSION: FDG PET is a potential biomarker for the prodromal stage of DLB. A higher medial temporal metabolism and CIS ratio, and lower substantia nigra metabolism have additive value in distinguishing prodromal DLB and AD.
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spelling pubmed-82784222021-07-19 FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD Kantarci, Kejal Boeve, Bradley F. Przybelski, Scott A. Lesnick, Timothy G. Chen, Qin Fields, Julie Schwarz, Christopher G. Senjem, Matthew L. Gunte, Jeffrey L. Jack, Clifford R. Min, Paul Jain, Manoj Migayawa, Toji Savica, Rodolfo Graff-Radford, Jonathan Botha, Hugo Jones, David T. Knopman, David S. Graff-Radford, Neill Ferman, Tanis J. Petersen, Ronald C. Lowe, Val J. Neuroimage Clin Regular Article BACKGROUND AND PURPOSE: Patients with dementia with Lewy bodies (DLB) are characterized by hypometabolism in the parieto–occipital cortex and the cingulate island sign (CIS) on (18)F-fluorodeoxyglucose (FDG) PET. Whether this pattern of hypometabolism is present as early as the prodromal stage of DLB is unknown. We investigated the pattern of hypometabolism in patients with mild cognitive impairment (MCI) who progressed to probable DLB compared to MCI patients who progressed to Alzheimer’s disease (AD) dementia and clinically unimpaired (CU) controls. METHODS: Patients with MCI from the Mayo Clinic Alzheimer’s Disease Research Center who underwent FDG PET at baseline and progressed to either probable DLB (MCI-DLB; n = 17) or AD dementia (MCI-AD; n = 41) during follow-up, and a comparison cohort of CU controls (n = 100) were included. RESULTS: Patients with MCI-DLB had hypometabolism in the parieto-occipital cortex extending into temporal lobes, substantia nigra and thalamus. When compared to MCI-AD, medial temporal and posterior cingulate metabolism were preserved in patients with MCI-DLB, accompanied by greater hypometabolism in the substantia nigra in MCI-DLB compared to MCI-AD. In distinguishing MCI-DLB from MCI-AD at the maximum value of Youden’s index, CIS ratio was highly specific (90%) but not sensitive (59%), but a higher medial temporal to substantia nigra ratio was both sensitive (94%) and specific (83%). CONCLUSION: FDG PET is a potential biomarker for the prodromal stage of DLB. A higher medial temporal metabolism and CIS ratio, and lower substantia nigra metabolism have additive value in distinguishing prodromal DLB and AD. Elsevier 2021-07-04 /pmc/articles/PMC8278422/ /pubmed/34252877 http://dx.doi.org/10.1016/j.nicl.2021.102754 Text en © 2021 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Kantarci, Kejal
Boeve, Bradley F.
Przybelski, Scott A.
Lesnick, Timothy G.
Chen, Qin
Fields, Julie
Schwarz, Christopher G.
Senjem, Matthew L.
Gunte, Jeffrey L.
Jack, Clifford R.
Min, Paul
Jain, Manoj
Migayawa, Toji
Savica, Rodolfo
Graff-Radford, Jonathan
Botha, Hugo
Jones, David T.
Knopman, David S.
Graff-Radford, Neill
Ferman, Tanis J.
Petersen, Ronald C.
Lowe, Val J.
FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD
title FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD
title_full FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD
title_fullStr FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD
title_full_unstemmed FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD
title_short FDG PET metabolic signatures distinguishing prodromal DLB and prodromal AD
title_sort fdg pet metabolic signatures distinguishing prodromal dlb and prodromal ad
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278422/
https://www.ncbi.nlm.nih.gov/pubmed/34252877
http://dx.doi.org/10.1016/j.nicl.2021.102754
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