Evidence map›Paper›PMID 42363718›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2026

Changes in DNA methylation-based aging predicts brain damage and dementia and reflects life-course cardiovascular risk.

Nigus Gebremedhin Asefa, Jorge Martinez Romero, Yi-Han Hu, Zhiguang Li, Osorio Meirelles, Djassinabaye Mbangdadji, May A Beydoun, Sigurdur Sigurdsson, Valborg Gudmundsdottir, Thor Aspelund and 2 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 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

12 authors.

Nigus Gebremedhin AsefaLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-5680-5527
Jorge Martinez RomeroLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.
Yi-Han HuLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.
Zhiguang LiLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.
Osorio MeirellesLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.
Djassinabaye MbangdadjiLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.
May A BeydounLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.
Sigurdur SigurdssonIcelandic Heart Association, Kopavogur, Iceland.
Valborg GudmundsdottirIcelandic Heart Association, Kopavogur, Iceland.
Thor AspelundIcelandic Heart Association, Kopavogur, Iceland.
Vilmundur GudnasonIcelandic Heart Association, Kopavogur, Iceland.
Lenore LaunerLaboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, Maryland, USA.

Funding

HjartaverndNIA NIH HHS
6 · The paper itself

Abstract

introductionThere is well-established evidence showing an association between accelerated biological aging (BA) and brain pathology. However, it remains unclear whether dynamic change in BA during adulthood is directly associated with brain health or primarily reflects cumulative life-course environmental and lifestyle exposures.

methodsWe analyzed data from the Age, Gene/Environment Susceptibility-Reykjavik Study (AGES-RS; n = 2081), with assessments at midlife (≈50 [SD 6.3] years) and late-life (baseline ≈76 [4.8]; follow-up ≈81 [4.8] years). We identified individuals with substantial change in BA (measured by DunedinPACE) and examined associations with brain magnetic resonance imaging (MRI) and cognitive outcomes. Mediation analyses tested whether late-life BA mediated associations between midlife cardiovascular health and later-life brain health.

resultsShifting to accelerated BA was associated with lower brain volumes and incident dementia. Associations with brain infarcts and cognitive function largely reflected cumulative life-course exposure. DISCUSSION: These findings underscore the need for further investigation into the timing, reversibility, and pathways linking BA to brain health.

Indexed as

AgingBrainCardiovascular DiseasesDementiaDNA MethylationAgedAged, 80 and overFemaleHeart Disease Risk FactorsHumansMagnetic Resonance ImagingMaleMiddle AgedRisk Factorsagingbiological agingbraincardiovascular healthdementiaDNA methylationlife‐courseLife's Simple 7lifestyle factorsmidlife

Identifiers

PMID42363718
PMCPMC13309854

What Socratic holds

Textmetadata
LicenceCC BY
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.