Evidence map›Paper›PMID 41567827›Full record

ArticleBrain communications2026

Brain age trajectories and cognition after stroke in two longitudinal cohorts.

Gisle Berg Helland, Håkon Ihle-Hansen, Anne Hege Aamodt, Esten H Leonardsen, Tobias Kaufmann, Brian Anthony B Enriquez, Mona K Beyer, Stein Andersson, Helle Stangeland, Hege Ihle-Hansen and 3 more

Abstract read
In one paragraph

Article in Brain communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

13 authors.

Gisle Berg HellandDepartment of Neurology, Oslo University Hospital, 0424 Oslo, Norway.ORCID https://orcid.org/0000-0003-2341-7733
Håkon Ihle-HansenDepartment of Medicine, Bærum Hospital, Vestre Viken Hospital Trust, 3004, Drammen, Norway.
Anne Hege AamodtDepartment of Neurology, Oslo University Hospital, 0424 Oslo, Norway.
Esten H LeonardsenInstitute of Clinical Medicine, University of Oslo, 0318, Oslo, Norway.
Tobias KaufmannInstitute of Clinical Medicine, University of Oslo, 0318, Oslo, Norway.
Brian Anthony B EnriquezDepartment of Neurology, Oslo University Hospital, 0424 Oslo, Norway.
Mona K BeyerInstitute of Clinical Medicine, University of Oslo, 0318, Oslo, Norway.ORCID https://orcid.org/0000-0001-9156-6357
Stein AnderssonDepartment of Psychology, University of Oslo, 0373, Oslo, Norway.
Helle StangelandDepartment of Research and Innovation, Division of Clinical Neuroscience, Oslo University Hospital, 0424, Oslo, Norway.ORCID https://orcid.org/0000-0001-8609-9926
Hege Ihle-HansenDepartment of Neurology, Oslo University Hospital, 0424 Oslo, Norway.
Hanne F HarboDepartment of Neurology, Oslo University Hospital, 0424 Oslo, Norway.
Einar August HøgestølDepartment of Neurology, Oslo University Hospital, 0424 Oslo, Norway.ORCID https://orcid.org/0000-0001-8446-2111
Guri HagbergDepartment of Neurology, Oslo University Hospital, 0424 Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain age is a promising neuroimaging biomarker, reflecting biological aging, but long-term trajectories and predictive value for cognitive outcomes post-stroke remains unclear. This study aimed to characterize brain aging trajectories over 8 years following a first-ever stroke and to evaluate the predictive value of brain age estimates for long-term cognitive outcomes. We analysed data from working-age (<65 years) ischaemic stroke patients with small- and medium-sized strokes (lesion volumes <70 ml), using two longitudinal stroke cohorts. T1-weighted MRI was acquired in the acute phase and at multiple time points up to 8 years post-stroke. Montreal cognitive assessment (MoCA) was assessed at follow-up sessions. Brain age was estimated using a state-of-the-art deep learning model. Brain-predicted age difference (Brain-PAD) was calculated as estimated brain age minus chronological age and corrected by regressing on age, age² and sex. Linear mixed-effects models examined Brain-PAD over multiple time points (whole-brain, ipsilesional and contralesional). Normalized brain volume was derived from FreeSurfer and included in the whole-brain analysis. Linear regression models evaluated whether brain age was associated with cognitive performance (MoCA) at long-term follow-up. We included 120 patients [

Indexed as

biomarkercognitionfollow-up studiesmachine learningstroke

Identifiers

PMID41567827
PMCPMC12816920

What Socratic holds

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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 Socratic graph.