Evidence map›Paper›PMID 39227310›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2024

Age differences in BOLD modulation to task difficulty as a function of amyloid burden.

Joseph P Hennessee, Tzu-Chen Lung, Denise C Park, Kristen M Kennedy

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

4 authors.

Joseph P HennesseeCenter for Vital Longevity; Department of Psychology, School of Behavioral and Brain Sciences, University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, United States.ORCID 0000-0002-1189-0649
Tzu-Chen LungCenter for Vital Longevity; Department of Psychology, School of Behavioral and Brain Sciences, University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, United States.
Denise C ParkCenter for Vital Longevity; Department of Psychology, School of Behavioral and Brain Sciences, University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, United States.
Kristen M KennedyCenter for Vital Longevity; Department of Psychology, School of Behavioral and Brain Sciences, University of Texas at Dallas, 1600 Viceroy Dr., Suite 800, Dallas, TX 75235, United States.

Funding

Neuroimaging of Dedifferentiation and Memory Across the LifespanR37AG006265 · NIA · UNIVERSITY OF TEXAS DALLAS · PI PARK, DENISE CORTIS · 2006 to 2016
$8.5M
Gag and Cyclophillin in HIV-1 ReplicationR01AI036199 · NIAID · UNIVERSITY OF GENEVA · PI LUBAN, JEREMY · 1994 to 2008
$2.9M
National Institutes of Health: National Institute on Aging 5R37AG-006265-27NIAID NIH HHS R01 AI036199NIA NIH HHS R37 AG006265
6 · The paper itself

Abstract

Effective cognitive performance often requires the allocation of additional neural resources (i.e. blood-oxygen-level-dependent [BOLD] activation) as task demands increase, and this demand-related modulation is affected by amyloid-beta deposition and normal aging. The present study investigated these complex relationships between amyloid, modulation, and cognitive function (i.e. fluid ability). Participants from the Dallas Lifespan Brain Study (DLBS, n = 252, ages 50-89) completed a semantic judgment task during functional magnetic resonance imaging (fMRI) where the judgments differed in classification difficulty. Amyloid burden was assessed via positron emission tomography (PET) using 18F-florbetapir. A quadratic relationship between amyloid standardized value uptake ratios (SUVRs) and BOLD modulation was observed such that modulation was weaker in those with moderately elevated SUVRs (e.g. just reaching amyloid-positivity), whereas those with very high SUVRs (e.g. SUVR > 1.5) showed strong modulation. Greater modulation was related to better fluid ability, and this relationship was strongest in younger participants and those with lower amyloid burden. These results support the theory that effective demand-related modulation contributes to healthy cognitive aging, especially in the transition from middle age to older adulthood, whereas high modulation may be dysfunctional in those with substantial amyloid deposition.

Indexed as

AgingBrainMagnetic Resonance ImagingPositron-Emission TomographyAgedAged, 80 and overAmyloid beta-PeptidesCognitionFemaleHumansMaleMiddle AgedOxygenAmyloid beta-PeptidesOxygenagingfluid intelligencefMRIPETsemantic

Identifiers

PMID39227310
PMCPMC11371418

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.