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Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults

The ability to accurately judge memory efficiency (meta-memory monitoring) for newly learned (episodic) information, is decreased in older adults and even worse in Alzheimer's disease (AD), whereas no differences have been found for semantic meta-memory. The pathological substrates of this phen...

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Autores principales: Vannini, Patrizia, Uquillas, Federico d'Oleire, Jacobs, Heidi I.L., Sepulcre, Jorge, Gatchel, Jennifer, Amariglio, Rebecca E., Hanseeuw, Bernard, Papp, Kathryn V., Hedden, Trey, Rentz, Dorene M., Pascual-Leone, Alvaro, Johnson, Keith A., Sperling, Reisa. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879982/
https://www.ncbi.nlm.nih.gov/pubmed/31795044
http://dx.doi.org/10.1016/j.nicl.2019.102097
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author Vannini, Patrizia
Uquillas, Federico d'Oleire
Jacobs, Heidi I.L.
Sepulcre, Jorge
Gatchel, Jennifer
Amariglio, Rebecca E.
Hanseeuw, Bernard
Papp, Kathryn V.
Hedden, Trey
Rentz, Dorene M.
Pascual-Leone, Alvaro
Johnson, Keith A.
Sperling, Reisa. A.
author_facet Vannini, Patrizia
Uquillas, Federico d'Oleire
Jacobs, Heidi I.L.
Sepulcre, Jorge
Gatchel, Jennifer
Amariglio, Rebecca E.
Hanseeuw, Bernard
Papp, Kathryn V.
Hedden, Trey
Rentz, Dorene M.
Pascual-Leone, Alvaro
Johnson, Keith A.
Sperling, Reisa. A.
author_sort Vannini, Patrizia
collection PubMed
description The ability to accurately judge memory efficiency (meta-memory monitoring) for newly learned (episodic) information, is decreased in older adults and even worse in Alzheimer's disease (AD), whereas no differences have been found for semantic meta-memory. The pathological substrates of this phenomenon are poorly understood. Here, we examine the association between meta-memory monitoring for episodic and semantic information to the two major proteinopathies in AD: amyloid (Aβ) and tau pathology in a group of cognitively unimpaired older adults. All participants underwent multi-tracer PET and meta-memory monitoring was assessed using a feeling-of-knowing (FOK) task for non-famous (episodic) and famous (semantic) face-name pairs. Whole brain voxel-wise correlations between meta-memory and PET data were conducted (controlling for memory), as well as confirmatory region-of-interest analyses. Participants had reduced episodic FOK compared to semantic FOK. Decreased episodic FOK was related to tauopathy in the medial temporal lobe regions, including the entorhinal cortex and temporal pole, whereas decreased semantic FOK was related to increased tau in regions associated with the semantic knowledge network. No association was found with Aβ-pathology. Alterations in the ability to accurately judge memory efficiency (in the absence of memory decline) may be a sensitive clinical indicator of AD pathophysiology in the pre-symptomatic phase.
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spelling pubmed-68799822019-11-29 Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults Vannini, Patrizia Uquillas, Federico d'Oleire Jacobs, Heidi I.L. Sepulcre, Jorge Gatchel, Jennifer Amariglio, Rebecca E. Hanseeuw, Bernard Papp, Kathryn V. Hedden, Trey Rentz, Dorene M. Pascual-Leone, Alvaro Johnson, Keith A. Sperling, Reisa. A. Neuroimage Clin Regular Article The ability to accurately judge memory efficiency (meta-memory monitoring) for newly learned (episodic) information, is decreased in older adults and even worse in Alzheimer's disease (AD), whereas no differences have been found for semantic meta-memory. The pathological substrates of this phenomenon are poorly understood. Here, we examine the association between meta-memory monitoring for episodic and semantic information to the two major proteinopathies in AD: amyloid (Aβ) and tau pathology in a group of cognitively unimpaired older adults. All participants underwent multi-tracer PET and meta-memory monitoring was assessed using a feeling-of-knowing (FOK) task for non-famous (episodic) and famous (semantic) face-name pairs. Whole brain voxel-wise correlations between meta-memory and PET data were conducted (controlling for memory), as well as confirmatory region-of-interest analyses. Participants had reduced episodic FOK compared to semantic FOK. Decreased episodic FOK was related to tauopathy in the medial temporal lobe regions, including the entorhinal cortex and temporal pole, whereas decreased semantic FOK was related to increased tau in regions associated with the semantic knowledge network. No association was found with Aβ-pathology. Alterations in the ability to accurately judge memory efficiency (in the absence of memory decline) may be a sensitive clinical indicator of AD pathophysiology in the pre-symptomatic phase. Elsevier 2019-11-18 /pmc/articles/PMC6879982/ /pubmed/31795044 http://dx.doi.org/10.1016/j.nicl.2019.102097 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Vannini, Patrizia
Uquillas, Federico d'Oleire
Jacobs, Heidi I.L.
Sepulcre, Jorge
Gatchel, Jennifer
Amariglio, Rebecca E.
Hanseeuw, Bernard
Papp, Kathryn V.
Hedden, Trey
Rentz, Dorene M.
Pascual-Leone, Alvaro
Johnson, Keith A.
Sperling, Reisa. A.
Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults
title Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults
title_full Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults
title_fullStr Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults
title_full_unstemmed Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults
title_short Decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults
title_sort decreased meta-memory is associated with early tauopathy in cognitively unimpaired older adults
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879982/
https://www.ncbi.nlm.nih.gov/pubmed/31795044
http://dx.doi.org/10.1016/j.nicl.2019.102097
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