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Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen

INTRODUCTION: Adults with Down syndrome (DS) are predisposed to Alzheimer's disease (AD) and the relationship between cognition and glucose metabolism in this population has yet to be evaluated. METHODS: Adults with DS (N = 90; mean age [standard deviation] = 38.0 [8.30] years) underwent [C‐11]...

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Autores principales: Zammit, Matthew D., Laymon, Charles M., Tudorascu, Dana L., Hartley, Sigan L., Piro‐Gambetti, Brianna, Johnson, Sterling C., Stone, Charles K., Mathis, Chester A., Zaman, Shahid H., Klunk, William E., Handen, Benjamin L., Cohen, Ann D., Christian, Bradley T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804861/
https://www.ncbi.nlm.nih.gov/pubmed/33490360
http://dx.doi.org/10.1002/dad2.12138
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author Zammit, Matthew D.
Laymon, Charles M.
Tudorascu, Dana L.
Hartley, Sigan L.
Piro‐Gambetti, Brianna
Johnson, Sterling C.
Stone, Charles K.
Mathis, Chester A.
Zaman, Shahid H.
Klunk, William E.
Handen, Benjamin L.
Cohen, Ann D.
Christian, Bradley T.
author_facet Zammit, Matthew D.
Laymon, Charles M.
Tudorascu, Dana L.
Hartley, Sigan L.
Piro‐Gambetti, Brianna
Johnson, Sterling C.
Stone, Charles K.
Mathis, Chester A.
Zaman, Shahid H.
Klunk, William E.
Handen, Benjamin L.
Cohen, Ann D.
Christian, Bradley T.
author_sort Zammit, Matthew D.
collection PubMed
description INTRODUCTION: Adults with Down syndrome (DS) are predisposed to Alzheimer's disease (AD) and the relationship between cognition and glucose metabolism in this population has yet to be evaluated. METHODS: Adults with DS (N = 90; mean age [standard deviation] = 38.0 [8.30] years) underwent [C‐11]Pittsburgh compound B (PiB) and [F‐18]fluorodeoxyglucose (FDG) positron emission tomography scans. Associations among amyloid beta (Aβ), FDG, and measures of cognition were explored. Interregional FDG metabolic connectivity was assessed to compare cognitively stable DS and mild cognitive impairment/AD (MCI‐DS/AD). RESULTS: Negative associations between Aβ and FDG were evident in regions affected in sporadic AD. A positive association was observed in the putamen, which is the brain region showing the earliest increases in Aβ deposition. Both Aβ and FDG were associated with measures of cognition, and metabolic connectivity distinguished cases of MCI‐DS/AD from cognitively stable DS. DISCUSSION: Associations among Aβ, FDG, and cognition reveal that neurodegeneration in DS resembles sporadic AD with the exception of the putamen, highlighting the usefulness of FDG in monitoring neurodegeneration in DS.
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spelling pubmed-78048612021-01-22 Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen Zammit, Matthew D. Laymon, Charles M. Tudorascu, Dana L. Hartley, Sigan L. Piro‐Gambetti, Brianna Johnson, Sterling C. Stone, Charles K. Mathis, Chester A. Zaman, Shahid H. Klunk, William E. Handen, Benjamin L. Cohen, Ann D. Christian, Bradley T. Alzheimers Dement (Amst) Diagnostic Assessment & Prognosis INTRODUCTION: Adults with Down syndrome (DS) are predisposed to Alzheimer's disease (AD) and the relationship between cognition and glucose metabolism in this population has yet to be evaluated. METHODS: Adults with DS (N = 90; mean age [standard deviation] = 38.0 [8.30] years) underwent [C‐11]Pittsburgh compound B (PiB) and [F‐18]fluorodeoxyglucose (FDG) positron emission tomography scans. Associations among amyloid beta (Aβ), FDG, and measures of cognition were explored. Interregional FDG metabolic connectivity was assessed to compare cognitively stable DS and mild cognitive impairment/AD (MCI‐DS/AD). RESULTS: Negative associations between Aβ and FDG were evident in regions affected in sporadic AD. A positive association was observed in the putamen, which is the brain region showing the earliest increases in Aβ deposition. Both Aβ and FDG were associated with measures of cognition, and metabolic connectivity distinguished cases of MCI‐DS/AD from cognitively stable DS. DISCUSSION: Associations among Aβ, FDG, and cognition reveal that neurodegeneration in DS resembles sporadic AD with the exception of the putamen, highlighting the usefulness of FDG in monitoring neurodegeneration in DS. John Wiley and Sons Inc. 2021-01-13 /pmc/articles/PMC7804861/ /pubmed/33490360 http://dx.doi.org/10.1002/dad2.12138 Text en © 2020 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Diagnostic Assessment & Prognosis
Zammit, Matthew D.
Laymon, Charles M.
Tudorascu, Dana L.
Hartley, Sigan L.
Piro‐Gambetti, Brianna
Johnson, Sterling C.
Stone, Charles K.
Mathis, Chester A.
Zaman, Shahid H.
Klunk, William E.
Handen, Benjamin L.
Cohen, Ann D.
Christian, Bradley T.
Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen
title Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen
title_full Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen
title_fullStr Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen
title_full_unstemmed Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen
title_short Patterns of glucose hypometabolism in Down syndrome resemble sporadic Alzheimer's disease except for the putamen
title_sort patterns of glucose hypometabolism in down syndrome resemble sporadic alzheimer's disease except for the putamen
topic Diagnostic Assessment & Prognosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804861/
https://www.ncbi.nlm.nih.gov/pubmed/33490360
http://dx.doi.org/10.1002/dad2.12138
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