Evidence map›Paper›PMID 41082658›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Sex differences in healthy brain aging are unlikely to explain higher Alzheimer's disease prevalence in women.

Anne Ravndal, Anders M Fjell, Didac Vidal-Piñeiro, Øystein Sørensen, Emilie S Falch, Julia Kropiunig, Pablo F Garrido, James M Roe, José-Luis Alatorre-Warren, Markus H Sneve and 13 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
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  4. Review
  5. 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

23 authors.

Anne RavndalCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0009-0008-4772-0386
Anders M FjellCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0003-2502-8774
Didac Vidal-PiñeiroCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0001-9997-9156
Øystein SørensenCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0003-0724-3542
Emilie S FalchCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0009-0000-0813-4394
Julia KropiunigCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0009-0009-3245-0923
Pablo F GarridoCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0002-6005-7178
James M RoeCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0002-8008-902X
José-Luis Alatorre-WarrenCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.
Markus H SneveCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0001-7644-7915
David Bartrés-FazDepartment of Medicine, Faculty of Medicine and Health Sciences and Neurosciences Institute, University of Barcelona, Barcelona 08036, Spain.
Alvaro Pascual-LeoneHinda and Arthur Marcus Institute for Aging Research and Deanna and Sidney Wolk Center for Memory Health, Hebrew SeniorLife, Boston, MA 02131.ORCID 0000-0001-8975-0382
Andreas M BrandmaierCenter for Lifespan Psychology, Max Planck Institute for Human Development, Berlin 14195, Germany.ORCID 0000-0001-8765-6982
Sandra DüzelCenter for Lifespan Psychology, Max Planck Institute for Human Development, Berlin 14195, Germany.
Simone KühnCenter for Lifespan Psychology, Max Planck Institute for Human Development, Berlin 14195, Germany.
Ulman LindenbergerCenter for Lifespan Psychology, Max Planck Institute for Human Development, Berlin 14195, Germany.ORCID 0000-0001-8428-6453
Lars NybergCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0002-3367-1746
Leiv Otto WatneOslo Delirium Research Group, Institute of Clinical Medicine, Campus Ahus, University of Oslo, Oslo 0318, Norway.
Richard N HensonMedical Research Council Cognition and Brain Sciences Unit, Department of Psychiatry, University of Cambridge, Cambridge CB2 7EF, United Kingdom.ORCID 0000-0002-0712-2639
Australian Imaging Biomarkers and Lifestyle flagship study of ageing (AIBL)
Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Kristine B WalhovdCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0003-1918-1123
Håkon GrydelandCenter for Lifespan Changes in Brain and Cognition, Department of Psychology, University of Oslo, Oslo 0317, Norway.ORCID 0000-0001-5061-464X

Funding

EC | European Research Council (ERC) 283634 725025EC | European Research Council (ERC) 313440Norwegian Research Council 249931Norwegian Research Council 324882Norwegian Research Council 325001 301395 239889Norwegian Research Council 325415Norwegian Research Council 325878 262453
6 · The paper itself

Abstract

As Alzheimer's disease (AD) is diagnosed more frequently in women, understanding the role of sex has become a key priority in AD research. However, despite aging being the primary risk factor for AD, it remains unclear whether men and women differ in the extent of brain decline with age. Using 12,638 longitudinal brain MRIs from 4,726 participants aged 17 to 95 y across 14 cohorts, we examined sex differences in structural brain changes over time, controlling for differences in head size. Men showed greater cortical thickness (CT) decline in the cuneus, lingual, parahippocampal, and pericalcarine regions; surface area decline in the fusiform and postcentral regions; and in older adults, greater subcortical decline in the caudate, nucleus accumbens, putamen, and pallidum. In contrast, women only showed greater surface area decline in the banks of the superior temporal sulcus and greater ventricular expansion in older adults. These results suggest that sex differences in age-related brain decline are unlikely to contribute to the higher AD diagnosis prevalence in women, necessitating research into alternative explanations.

Indexed as

AgingAlzheimer DiseaseBrainSex CharacteristicsAdolescentAdultAgedAged, 80 and overFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle AgedPrevalenceSex FactorsAlzheimer’s diseasebrain aginglongitudinal imagingMRIsex differences

Identifiers

PMID41082658
PMCPMC12557495

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.