Evidence map›Paper›PMID 36969093›Full record

ArticleNeuroimage. Reports2023

Polygenic indices for cognition in healthy aging; the role of brain measures.

A Tsapanou, N Mourtzi, Y Gu, C Habeck, D Belsky, Y Stern

Abstract read
In one paragraph

Article in Neuroimage. Reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. 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

6 authors.

A TsapanouCognitive Neuroscience Division, Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.
N Mourtzi1st Department of Neurology, Aiginition Hospital, National and Kapodistrian University of Athens Medical School, Athens, Greece.
Y GuCognitive Neuroscience Division, Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.
C HabeckCognitive Neuroscience Division, Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.
D BelskyDepartment of Epidemiology, Columbia University Mailman School of Public Health, New York, USA.
Y SternCognitive Neuroscience Division, Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.

Funding

Exploring Cognitive Aging Using Reference Ability Neural NetworksR01AG038465 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HABECK, CHRISTIAN GEORG, STERN, YAAKOV · 2011 to 2025
$17.0M
Imaging of Cognition, Learning and Memory in AgingR01AG026158 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI STERN, YAAKOV · 2004 to 2021
$10.9M
Statistical method for neural mechanism mediating and moderating cognitive system in Alzheimer's disease and aging research.R01AG062578 · NIA · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI LEE, SEONJOO · 2020 to 2024
$2.1M
Longitudinal changes in white matter integrity predicting cognitive changes in reasoning and vocabulary abilitiesK01AG051777 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GAZES, YUNGLIN · 2016 to 2020
$623k
Sleep duration Polygenic Risk Score: Association with cognition and brain measuresK99AG071930 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TSAPANOU, ANGELIKI · 2022 to 2023
$261k
NIA NIH HHS K01 AG051777NIA NIH HHS K99 AG071930NIA NIH HHS R01 AG026158NIA NIH HHS R01 AG038465NIA NIH HHS R01 AG062578
6 · The paper itself

Abstract

Background: Genome-wide association studies (GWAS) have identified large numbers of genetic variants associated with cognition. However, little is known about how these genetic discoveries impact cognitive aging. Methods: We conducted polygenic-index (PGI) analysis of cognitive performance in n = 168 European-ancestry adults aged 20-80. We computed PGIs based on GWAS of cognitive performance in young/middle-aged and older adults. We tested associations of the PGI with cognitive performance, as measured through neuropsychological evaluation. We explored whether these associations were accounted for by magnetic resonance imaging (MRI) measures of brain-aging phenotypes: total gray matter volume (GM), cortical thickness (CT), and white matter hyperintensities burden (WMH). Results: Participants with higher PGI values performed better on cognitive tests (B = 0.627, SE = 0.196, Conclusions: Genetics discovered in GWAS of cognition are associated with cognitive performance in healthy adults across age, but most strongly in young and middle-aged adults. Associations were not explained by brain-structural markers of brain aging. Genetics uncovered in GWAS of cognitive performance may contribute to individual differences established relatively early in life and may not reflect genetic mechanisms of cognitive aging.

Indexed as

Brain morphometryCognitionCognitive agingNeural phenotypesPolygenic indices

Identifiers

PMID36969093
PMCPMC10038095

What OpenQuestion holds

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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.