Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloid

Abstract Introduction In cognitively normal (CN) adults, increased rates of amyloid beta (Aβ) accumulation can be detected in low Aβ (Aβ–) apolipoprotein E (APOE) ε4 carriers. We aimed to determine the effect of ε4 on the ability to benefit from experience (ie, learn) in Aβ– CNs. Methods Aβ– CNs (n ...

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Main Authors: Yen Ying Lim, Jenalle E. Baker, Andrea Mills, Loren Bruns Jr, Christopher Fowler, Jurgen Fripp, Stephanie R. Rainey‐Smith, David Ames, Colin L Masters, Paul Maruff
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
Subjects:
Online Access:https://doi.org/10.1002/dad2.12136
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author Yen Ying Lim
Jenalle E. Baker
Andrea Mills
Loren Bruns Jr
Christopher Fowler
Jurgen Fripp
Stephanie R. Rainey‐Smith
David Ames
Colin L Masters
Paul Maruff
author_facet Yen Ying Lim
Jenalle E. Baker
Andrea Mills
Loren Bruns Jr
Christopher Fowler
Jurgen Fripp
Stephanie R. Rainey‐Smith
David Ames
Colin L Masters
Paul Maruff
author_sort Yen Ying Lim
collection DOAJ
description Abstract Introduction In cognitively normal (CN) adults, increased rates of amyloid beta (Aβ) accumulation can be detected in low Aβ (Aβ–) apolipoprotein E (APOE) ε4 carriers. We aimed to determine the effect of ε4 on the ability to benefit from experience (ie, learn) in Aβ– CNs. Methods Aβ– CNs (n = 333) underwent episodic memory assessments every 18 months for 108 months. A subset (n = 48) completed the Online Repeatable Cognitive Assessment‐Language Learning Test (ORCA‐LLT) over 6 days. Results Aβ– ε4 carriers showed significantly lower rates of improvement on episodic memory over 108 months compared to non‐carriers (d = 0.3). Rates of learning on the ORCA‐LLT were significantly slower in Aβ– ε4 carriers compared to non‐carriers (d = 1.2). Discussion In Aβ– CNs, ε4 is associated with a reduced ability to benefit from experience. This manifested as reduced practice effects (small to moderate in magnitude) over 108 months on the episodic memory composite, and a learning deficit (large in magnitude) over 6 days on the ORCA‐LLT. Alzheimer's disease (AD)–related cognitive abnormalities can manifest before preclinical AD thresholds.
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spelling doaj.art-29e1c02bde994115af43b8750883003a2022-12-28T09:12:14ZengWileyAlzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring2352-87292021-01-01131n/an/a10.1002/dad2.12136Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloidYen Ying Lim0Jenalle E. Baker1Andrea Mills2Loren Bruns Jr3Christopher Fowler4Jurgen Fripp5Stephanie R. Rainey‐Smith6David Ames7Colin L Masters8Paul Maruff9Turner Institute for Brain and Mental Health, School of Psychological Sciences Monash University Clayton Victoria AustraliaThe Florey Institute of Neuroscience and Mental Health University of Melbourne Parkville Victoria AustraliaTurner Institute for Brain and Mental Health, School of Psychological Sciences Monash University Clayton Victoria AustraliaSchool of Computing and Information Systems University of Melbourne Parkville Victoria AustraliaThe Florey Institute of Neuroscience and Mental Health University of Melbourne Parkville Victoria AustraliaCSIRO Health and Biosecurity Australian e‐Health Research Centre Brisbane Queensland AustraliaCentre of Excellence for Alzheimer's Disease Research and Care, School of Medical Sciences Edith Cowan University Perth Western Australia AustraliaNational Ageing Research Institute Parkville Victoria AustraliaThe Florey Institute of Neuroscience and Mental Health University of Melbourne Parkville Victoria AustraliaThe Florey Institute of Neuroscience and Mental Health University of Melbourne Parkville Victoria AustraliaAbstract Introduction In cognitively normal (CN) adults, increased rates of amyloid beta (Aβ) accumulation can be detected in low Aβ (Aβ–) apolipoprotein E (APOE) ε4 carriers. We aimed to determine the effect of ε4 on the ability to benefit from experience (ie, learn) in Aβ– CNs. Methods Aβ– CNs (n = 333) underwent episodic memory assessments every 18 months for 108 months. A subset (n = 48) completed the Online Repeatable Cognitive Assessment‐Language Learning Test (ORCA‐LLT) over 6 days. Results Aβ– ε4 carriers showed significantly lower rates of improvement on episodic memory over 108 months compared to non‐carriers (d = 0.3). Rates of learning on the ORCA‐LLT were significantly slower in Aβ– ε4 carriers compared to non‐carriers (d = 1.2). Discussion In Aβ– CNs, ε4 is associated with a reduced ability to benefit from experience. This manifested as reduced practice effects (small to moderate in magnitude) over 108 months on the episodic memory composite, and a learning deficit (large in magnitude) over 6 days on the ORCA‐LLT. Alzheimer's disease (AD)–related cognitive abnormalities can manifest before preclinical AD thresholds.https://doi.org/10.1002/dad2.12136Alzheimer's diseaseamyloidapolipoprotein Elearningmemory
spellingShingle Yen Ying Lim
Jenalle E. Baker
Andrea Mills
Loren Bruns Jr
Christopher Fowler
Jurgen Fripp
Stephanie R. Rainey‐Smith
David Ames
Colin L Masters
Paul Maruff
Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloid
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring
Alzheimer's disease
amyloid
apolipoprotein E
learning
memory
title Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloid
title_full Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloid
title_fullStr Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloid
title_full_unstemmed Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloid
title_short Learning deficit in cognitively normal APOE ε4 carriers with LOW β‐amyloid
title_sort learning deficit in cognitively normal apoe ε4 carriers with low β amyloid
topic Alzheimer's disease
amyloid
apolipoprotein E
learning
memory
url https://doi.org/10.1002/dad2.12136
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