Evidence map›Paper›PMID 36481934›Full record

ArticleMolecular psychiatry2023

Predictors of longitudinal cognitive ageing from age 70 to 82 including APOE e4 status, early-life and lifestyle factors: the Lothian Birth Cohort 1936.

Janie Corley, Federica Conte, Sarah E Harris, Adele M Taylor, Paul Redmond, Tom C Russ, Ian J Deary, Simon R Cox

Open access · hybridFull text read
In one paragraph

Article in Molecular psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  6. Cognitive dedifferentiation in later life: longitudinal findings from the Lothian Birth Cohort 1936.The journals of gerontology. Series B, Psychological sciences and social sciences · 2026
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  10. Review
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  13. Early cognitive ability and dementia risk: Response to Chen and colleagues.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  14. Article
  15. A lifespan perspective on cognitive reserve and risk for dementia.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  16. Modifiable Risk Factors for Cognitive Decline in Community-Dwelling Older Adults Differ by Sex and APOE4.The journals of gerontology. Series B, Psychological sciences and social sciences · 2025
    Article
  17. Lessons we learned from the Lothian Birth Cohorts of 1921 and 1936.Genomic psychiatry : advancing science from genes to society · 2025
    Article
  18. Article
  19. Article
  20. Differences in Alzheimer's Disease-Related Pathology Profiles Across Apolipoprotein Groups.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Article
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

8 authors at 2 institutions in 2 countries.

Janie CorleyLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK. Janie.Corley@ed.ac.uk.ORCID 0000-0002-7551-1871
Federica ConteDepartment of Psychology, University of Milano-Bicocca, Milan, Italy.ORCID 0000-0001-8064-1075
Sarah E HarrisLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-4941-5106
Adele M TaylorLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Paul RedmondLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Tom C RussLothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Ian J Deary *Lothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.
Simon R Cox *Lothian Birth Cohorts, Department of Psychology, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-4036-3642
NHS Lothian · GBUniversity of Milano-Bicocca · IT

Funding

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
Medical Research Council G0700704Medical Research Council G0701120Medical Research Council G1001245Medical Research Council MR/M013111/1Medical Research Council MR/R024065/1NIA NIH HHS R01 AG054628Wellcome Trust
6 · The paper itself

Abstract

Discovering why some people's cognitive abilities decline more than others is a key challenge for cognitive ageing research. The most effective strategy may be to address multiple risk factors from across the life-course simultaneously in relation to robust longitudinal cognitive data. We conducted a 12-year follow-up of 1091 (at age 70) men and women from the longitudinal Lothian Birth Cohort 1936 study. Comprehensive repeated cognitive measures of visuospatial ability, processing speed, memory, verbal ability, and a general cognitive factor were collected over five assessments (age 70, 73, 76, 79, and 82 years) and analysed using multivariate latent growth curve modelling. Fifteen life-course variables were used to predict variation in cognitive ability levels at age 70 and cognitive slopes from age 70 to 82. Only APOE e4 carrier status was found to be reliably informative of general- and domain-specific cognitive decline, despite there being many life-course correlates of cognitive level at age 70. APOE e4 carriers had significantly steeper slopes across all three fluid cognitive domains compared with non-carriers, especially for memory (β = -0.234, p < 0.001) and general cognitive function (β = -0.246, p < 0.001), denoting a widening gap in cognitive functioning with increasing age. Our findings suggest that when many other candidate predictors of cognitive ageing slope are entered en masse, their unique contributions account for relatively small proportions of variance, beyond variation in APOE e4 status. We conclude that APOE e4 status is important for identifying those at greater risk for accelerated cognitive ageing, even among ostensibly healthy individuals.

Indexed as

Cognitive AgingCognitive DysfunctionAgedAged, 80 and overApolipoprotein E4Apolipoproteins EBirth CohortCognitionFemaleHumansLife StyleLongitudinal StudiesMaleNeuropsychological TestsApolipoprotein E4Apolipoproteins E

Identifiers

PMID36481934
PMCPMC10005946
OpenAlexW4310963102

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read64
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.