Evidence map›Paper›PMID 42566156›Full record

ArticleGeroScience2026

Identification and phenotypic profiling of subgroups with distinct cognitive aging trajectories.

Lydia M Federmann, Christian Mychajliw, Ulrike Sünkel, Didem Stark, Serli Kopar, Daniela Berg, Kathrin Brockmann, Andreas Fallgatter, Clint Hansen, Sebastian Heinzel and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in GeroScience, 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

15 authors.

Lydia M FedermannHertie Institute for AI in Brain Health, University of Tübingen, Tübingen, Germany. lydia-marie.federmann@uni-tuebingen.de.ORCID http://orcid.org/0009-0006-4500-2175
Christian MychajliwGeriatric Centre at the University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-9234-6046
Ulrike SünkelDepartment of Psychiatry and Psychotherapy, University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-5348-3996
Didem StarkHertie Institute for AI in Brain Health, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-7275-0359
Serli KoparHertie Institute for AI in Brain Health, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-1409-2896
Daniela BergDepartment of Neurology, University Hospital Schleswig-Holstein and Kiel University, Kiel, Germany.ORCID http://orcid.org/0000-0001-5796-5442
Kathrin BrockmannCenter of Neurology, University Hospital Tübingen and Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-7515-8596
Andreas FallgatterDepartment of Psychiatry and Psychotherapy, University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-7713-4259
Clint HansenDepartment of Neurology, University Hospital Schleswig-Holstein and Kiel University, Kiel, Germany.ORCID http://orcid.org/0000-0003-4813-3868
Sebastian HeinzelDepartment of Neurology, University Hospital Schleswig-Holstein and Kiel University, Kiel, Germany.ORCID http://orcid.org/0000-0003-4516-0529
Walter MaetzlerDepartment of Neurology, University Hospital Schleswig-Holstein and Kiel University, Kiel, Germany.ORCID http://orcid.org/0000-0002-5945-4694
Florian MetzgerGeriatric Centre at the University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-8236-1170
Anna-Katharina von ThalerGeriatric Centre at the University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-8161-5813
Gerhard W EschweilerGeriatric Centre at the University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0009-0007-2630-5928
Kerstin RitterHertie Institute for AI in Brain Health, University of Tübingen, Tübingen, Germany. kerstin.ritter@uni-tuebingen.de.ORCID http://orcid.org/0000-0001-7115-0020

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive aging is shaped by genetic variation, environmental factors, and health-related conditions. Until now, it is largely unclear why some individuals maintain their cognitive function, and others show progressive cognitive decline. This study uncovered determinants of distinct cognitive aging trajectories in the older population. To approach the inter-individual variability in cognitive aging, we clustered n = 696 dementia-free individuals from the prospective TREND study based on their longitudinal changes in comprehensive cognitive testing every 2 years over 13 years on average. Identified subgroups of cognitive aging were tested for differences in general physical health, motor function, mental and neuropsychological health, personality, lifestyle, diet, and genetic and biofluid markers as observed at the phenotypes' initial records. Comparing the best- and lowest-performing subgroups of cognitive aging, we found that individuals who maintain high cognitive function compared to those with low baseline and progressive cognitive decline showed significant faster gait speed, higher health-related quality of life, did sports and cognitive stimulating activities more frequently, and reported higher plant-based foods intake. Although there are fewer phenotypic differences involving the intermediate subgroups of cognitive aging, the best-performing subgroup compared to all other subgroups showed higher plant-based foods intake. Overall, this study identifies distinct, data-driven subgroups of long-term cognitive aging trajectories and reveals factors associated with these divergent paths using deeply phenotyped data. The findings highlight the substantial heterogeneity of cognitive aging and suggest that favorable trajectories are linked to modifiable behavioral and health-related characteristics, providing a foundation for future multidisciplinary strategies to promote healthy cognitive aging.

Indexed as

Aging heterogeneityCognitive agingCognitive maintenanceHealthy agingLongitudinal data analysisTrajectory modeling

Identifiers

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.