Evidence map›Paper›PMID 41053433›Full record

ArticleMolecular psychiatry2026

Effect sizes of APOE e4 on the same general cognitive ability test taken by the same people from age 11 to age 90: The Lothian Birth Cohorts 1921 and 1936.

Ian J Deary, Sarah E Harris, Tom C Russ, Simon R Cox, Janie Corley

Abstract read
In one paragraph

Article in Molecular psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Prosocial helping behaviors attenuate accelerated cognitive decline driven by APOE ε4.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Ian J Deary *Lothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, United Kingdom. i.deary@ed.ac.uk.ORCID 0000-0002-1733-263X
Sarah E HarrisLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0002-4941-5106
Tom C RussAlzheimer Scotland Dementia Research Centre, Department of Psychology, University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0001-9797-2188
Simon R CoxLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0003-4036-3642
Janie Corley *Lothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, United Kingdom. Janie.Corley@ed.ac.uk.ORCID 0000-0002-7551-1871

Funding

Longitudinal multi-omic biomarkers for neurocognitive decline prior to dementia onsetU01AG083829 · NIA · UNIVERSITY OF EDINBURGH · PI Sarah Elizabeth Harris · 2024 to 2026
$3.5M
Evaluating Longitudinal Changes in the Human Structural Connectome in Relation to Cognitive AgingR01AG054628 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI TUCKER-DROB, ELLIOT MAX · 2017 to 2021
$2.7M
NIA NIH HHS R01 AG054628NIA NIH HHS U01 AG083829RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/W008793/1RCUK | Medical Research Council (MRC) MR/X003434/1RCUK | MRC | Medical Research Foundation MR/X003434/1U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AG054628, U01AG083829U.S. Department of Health & Human Services | National Institutes of Health (NIH) U01AG083829Wellcome TrustWellcome Trust (Wellcome) 221890/Z/20/Z
6 · The paper itself

Abstract

Variation in the gene for apolipoprotein E (APOE) is one of the few variables that is associated with individual differences in age-related cognitive decline in humans. Therefore, it is important to understand the conditions that affect the strength of its effect. Here we examine how the effect size of APOE variation (possession of one or more e4 alleles) on a test of general cognitive ability changes with age from 11-90 years. The data are from the Lothian Birth Cohorts of 1936 and 1921 who took the same cognitive test (the Moray House Test No. 12) at, respectively, ages 11 (N = 954), 70 (N = 1001), 76 (N = 636), 79 (N = 471), and 11 (N = 483), 79 (N = 533), 87 (N = 198), 90 (N = 120). The standardised absolute effect of APOE e4 on general cognitive ability was about zero at ages 11 (beta < 0.05) and 70 (beta ≤ 0.025) and increased linearly to beta = 0.30 (p < 0.001) at age 90. The effect sizes were minimally affected by adjusting for medical conditions (hypertension, diabetes, cardiovascular disease, stroke). However, the results were less robust to removing those participants who developed dementia; effect sizes were reduced by about a third to a half, and were largely non-significant. The results suggest that the negative effect of APOE e4 on cognitive functioning becomes greater with age; this urges more work to understand the mechanisms by which e4 status renders the older person's brain increasingly vulnerable to cognitive decline and dementia.

Indexed as

Apolipoprotein E4CognitionAdolescentAdultAgedAged, 80 and overAgingAllelesApolipoproteins EBirth CohortChildCognitive DysfunctionCohort StudiesFemaleGenotypeHumansApolipoprotein E4Apolipoproteins E

Identifiers

PMID41053433
PMCPMC12700797

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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.