Evidence map›Paper›PMID 28652414›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

Differential Aging Trajectories of Modulation of Activation to Cognitive Challenge in APOE ε4 Groups: Reduced Modulation Predicts Poorer Cognitive Performance.

Chris M Foster, Kristen M Kennedy, Karen M Rodrigue

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Chris M FosterCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, Dallas, Texas 75235.ORCID 0000-0001-5049-6049
Kristen M KennedyCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, Dallas, Texas 75235.ORCID 0000-0001-5373-9026
Karen M RodrigueCenter for Vital Longevity, School of Behavioral and Brain Sciences, The University of Texas at Dallas, Dallas, Texas 75235 krodrigue@utdallas.edu.ORCID 0000-0002-4781-7961
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
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
Role of White Matter Integrity in Age-Related Functional ReorganizationK99AG036818 · NIA · UNIVERSITY OF TEXAS DALLAS · PI KENNEDY, KRISTEN M. · 2010 to 2011
$179k
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 AG036818NIA NIH HHS K99 AG036848NIA NIH HHS R00 AG036818NIA NIH HHS R00 AG036848NIA NIH HHS R01 AG056535
6 · The paper itself

Abstract

The present study was designed to investigate the effect of a genetic risk factor for Alzheimer's disease (AD), ApolipoproteinE ε4 (APOEε4), on the ability of the brain to modulate activation in response to cognitive challenge in a lifespan sample of healthy human adults. A community-based sample of 181 cognitively intact, healthy adults were recruited from the Dallas-Fort Worth metroplex. Thirty-one APOEε4+ individuals (48% women), derived from the parent sample, were matched based on sex, age, and years of education to 31 individuals who were APOEε4-negative (APOEε4-). Ages ranged from 20 to 86 years of age. Blood oxygen level-dependent functional magnetic resonance imaging was collected during the performance of a visuospatial distance judgment task with three parametric levels of difficulty. Multiple regression was used in a whole-brain analysis with age, APOE group, and their interaction predicting functional brain modulation in response to difficulty. Results revealed an interaction between age and APOE in a large cluster localized primarily to the bilateral precuneus. APOEε4- individuals exhibited age-invariant modulation in response to task difficulty, whereas APOEε4+ individuals showed age-related reduction of modulation in response to increasing task difficulty compared with ε4- individuals. Decreased modulation in response to cognitive challenge was associated with reduced task accuracy as well as poorer name-face associative memory performance. Findings suggest that APOEε4 is associated with a reduction in the ability of the brain to dynamically modulate in response to cognitive challenge. Coupled with a significant genetic risk factor for AD, changes in modulation may provide additional information toward identifying individuals potentially at risk for cognitive decline associated with preclinical AD.

Indexed as

AdultAgedAged, 80 and overAgingApolipoprotein E4BrainCognitionExecutive FunctionFemaleGenetic MarkersHumansMaleMemoryMiddle AgedApolipoprotein E4Genetic MarkersagingAPOEcognitionfMRI

Identifiers

PMID28652414
PMCPMC5518419
OpenAlexW2665919687

What OpenQuestion holds

Textmetadata
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.