Evidence map›Paper›PMID 42428989›Full record

ArticleCommunications health2026

Adverse childhood experiences, early menopause, cognition, and dementia in older adults in the United States.

Miharu Nakanishi, Jordan DeVylder, Gemma Knowles, Masato Hasegawa, Marcus Richards, Atsushi Nishida

Abstract read
In one paragraph

Article in Communications health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Miharu NakanishiDepartment of Psychiatric Nursing, Graduate School of Medicine, Tohoku University, Sendai-shi, Japan.
Jordan DeVylderNYU Silver School of Social Work, New York, NY USA.
Gemma KnowlesHealth Service and Population Research Department, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Masato HasegawaDementia Research Project, Tokyo Metropolitan Institute of Medical Science, Setagaya-ku, Japan.
Marcus RichardsUnit for Lifelong Health and Ageing at UCL, Faculty of Population Health Sciences, University College London, London, UK.
Atsushi NishidaResearch Center for Social Science and Medicine, Tokyo Metropolitan Institute of Medical Science, Setagaya-ku, Japan.

Funding

HRS Yrs29-34: Y33 SSA CoFundingU01AG009740 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jessica Faul, KENNETH M LANGA · 1990 to 2026
$555.8M
NIA NIH HHS U01 AG009740Wellcome Trust
6 · The paper itself

Abstract

Background: Adverse childhood experiences (ACEs) may accelerate early menopause and influence neurodegenerative processes, contributing to sex-specific dementia risk. This study examined associations with cognitive decline and incident dementia in ACEs and early menopause. Methods: We studied 6093 women and 5784 men aged ≥50 years from the Health and Retirement Study, a US cohort spanning between 2010 and 2022. Incident dementia was based on self-report of physician-diagnosed dementia. Cognition was measured using a composite score of immediate and delayed recall, serial sevens subtraction, and counting backwards (range, 0-27). ACEs were assessed using seven items and classified into none, 1, 2, and ≥3 ACEs. Age at menopause was classified into <47, 47 to 52, and ≥53 years. We included men and defined the four categories of sex and age at menopause, assessing varying levels of female hormones with age at menopause serving as the proxy indicator of those differences. Covariates included lifestyle risk factors for dementia. We used a longitudinal panel design with each observation containing baseline covariates and 2-year follow-up outcomes. We applied a random-effects model to survival analysis for incident dementia and to linear regression analysis for cognition. Results: Here we show that experiencing 2 (hazard ratio: 1.32 [95% CI: 1.07-1.62]) or ≥3 ACEs (1.32 [1.03-1.68]) is associated with higher dementia risk compared with no ACEs. Dementia risk does not differ by sex and age at menopause in women. Women with early menopause ( Conclusions: Mechanisms linking ACEs and early menopause to dementia risk may differ. Risk reduction strategies should consider preventing and addressing ACEs and early menopause, respectively.

Indexed as

DiseasesHealth careMedical researchNeurologyNeuroscienceRisk factors

Identifiers

PMID42428989
PMCPMC13347797

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.