Evidence map›Paper›PMID 32736001›Full record

ArticleNeuroImage2020

Beta-amyloid burden predicts poorer mnemonic discrimination in cognitively normal older adults.

Christina E Webb, Chris M Foster, Marci M Horn, Kristen M Kennedy, Karen M Rodrigue

Open access · goldAbstract read
In one paragraph

Article in NeuroImage, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  3. Trial
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  5. Synergistic effects ofbioRxiv : the preprint server for biology · 2025
    Article
  6. Amyloid-Beta Deposition in Basal Frontotemporal Cortex Is Associated with Selective Disruption of Temporal Mnemonic Discrimination.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Christina E WebbCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, USA.
Chris M FosterCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, USA.
Marci M HornCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, USA.
Kristen M KennedyCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, USA.
Karen M RodrigueCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, USA. Electronic address: krodrigue@utdallas.edu.
The University of Texas at Dallas · US

Funding

Dopaminergic and Neuroplastic Influences on Longitudinal Change in Cognitive and Brain AgingR01AG056535 · NIA · UNIVERSITY OF TEXAS DALLAS · PI Kristen M. Kennedy, Karen M Rodrigue · 2017 to 2026
$4.8M
Mechanisms and Predictors of Brain Aging in Healthy Aging, Preclinical AD and MCIR01AG057537 · NIA · UNIVERSITY OF TEXAS DALLAS · PI RODRIGUE, KAREN M · 2018 to 2022
$3.5M
Role of White Matter Integrity in Age-Related Functional ReorganizationR00AG036818 · NIA · UNIVERSITY OF TEXAS DALLAS · PI KENNEDY, KRISTEN M. · 2012 to 2014
$733k
Vascular Effects on Normal Neural and Cognitive AgingR00AG036848 · NIA · UNIVERSITY OF TEXAS DALLAS · PI RODRIGUE, KAREN M · 2012 to 2014
$733k
Vascular Effects on Normal Neural and Cognitive AgingK99AG036848 · NIA · UNIVERSITY OF TEXAS DALLAS · PI RODRIGUE, KAREN M · 2010 to 2011
$179k
NIA NIH HHS K99 AG036848NIA NIH HHS R00 AG036818NIA NIH HHS R00 AG036848NIA NIH HHS R01 AG056535NIA NIH HHS R01 AG057537
6 · The paper itself

Abstract

One of the earliest indicators of Alzheimer's disease pathology is the presence of beta-amyloid (Αβ) protein deposition. Significant amyloid deposition is evident even in older adults who exhibit little or no overt cognitive or memory impairment. Hippocampal-based processes that help distinguish between highly similar memory representations may be the most susceptible to early disease pathology. Amyloid associations with memory have been difficult to establish, possibly because typical memory assessments do not tax hippocampal operations sufficiently. Thus, the present study utilized a spatial mnemonic discrimination task designed to tax hippocampal pattern separation/completion processes in a sample of cognitively normal middle-aged and older adults (53-98 years old) who underwent PET

Indexed as

NeuroimagingPositron-Emission TomographyAgedAged, 80 and overAmyloid beta-PeptidesAniline CompoundsCognitive AgingEthylene GlycolsFemaleHippocampusHumansMaleMiddle AgedRecognition, PsychologySpatial MemoryAmyloid beta-PeptidesAniline CompoundsEthylene GlycolsflorbetapirBeta-amyloidCognitive agingMemoryMnemonic discriminationPreclinical Alzheimer's disease

Identifiers

PMID32736001
PMCPMC7813158
OpenAlexW3045899671

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.