Evidence map›Paper›PMID 40781909›Full record

ArticleAnnals of neurology2025

Protective Effects of Socioeconomic Status and Lifestyle on Amyloid- and White Matter Hyperintensity-Related Longitudinal Brain Atrophy and Cognitive Decline.

Dario Bachmann, Maha Wybitul, Sandro Studer, Antje Saake, Katrin Rauen, Andreas Buchmann, Bettina von Rickenbach, Esmeralda Gruber, Roger M Nitsch, Christoph Hock and 2 more

Erratum issuedAbstract read
In one paragraph

Article in Annals of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Dario BachmannInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-2863-537X
Maha WybitulInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Sandro StuderInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Antje SaakeInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Katrin RauenInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.ORCID 0000-0003-4555-6697
Andreas BuchmannInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Bettina von RickenbachClinic for Aging Medicine, Hospital Affoltern, Affoltern, Switzerland.
Esmeralda GruberInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Roger M NitschInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Christoph HockInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Anton GietlInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.
Valerie TreyerInstitute for Regenerative Medicine, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-4584-3031

Funding

Mäxi-StiftungVontobel-Stiftung
6 · The paper itself

Abstract

objectiveSocioeconomic status (SES) and lifestyle activities (LA) are strongly related, and both are associated with dementia risk. We investigated the influence of SES and LA on brain atrophy and cognitive decline considering amyloid-beta (Aβ) positron emission tomography and white matter hyperintensity (WMH) load.

methodsWe investigated 221 older adults (mean age, 67.1 ± 8.2 years) who underwent cognitive testing annually over a median follow-up period of 3.4 years. Longitudinal T1-weighted magnetic resonance imaging was available for 181 participants. Measures of SES and LA were collected using questionnaires and combined to SES and LA scores using a latent variable approach. We used linear mixed-effects models to investigate if SES and LA are independently or interactively with Aβ and WMH load associated with decline in domains language, processing speed/attention, executive function, and episodic memory. Mediation models assessed whether these associations were explained by gray matter atrophy.

resultsSES and LA were associated with better cognitive performance at baseline, but were not associated with cognitive decline over time. In interaction with brain pathologies, higher LA reduced the detrimental effects of Aβ and WMH load on language decline, whereas higher SES reduced the detrimental effects of Aβ pathology on episodic memory decline. Individuals with low SES showed faster Aβ-related gray matter atrophy, which mediated the association between Aβ and episodic memory decline but not language decline.

interpretationThese results suggest that multiple resilience mechanisms underlie the protective effects of SES and LA on cognitive decline. Interventions targeting SES-related risk factors may be most effective when implemented early, before neurodegenerative changes begin. ANN NEUROL 2025;98:1222-1236.

Indexed as

Amyloid beta-PeptidesBrainCognitive DysfunctionLife StyleSocial ClassWhite MatterAgedAtrophyFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle AgedNeuropsychological TestsPositron-Emission TomographyAmyloid beta-Peptides

Identifiers

PMID40781909
PMCPMC12682946

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LicenceCC BY
Read underepoch 390

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.