Evidence map›Paper›PMID 37574523›Full record

ArticleTranslational psychiatry2023

Age-, sex-, and pathology-related variability in brain structure and cognition.

Dario Bachmann, Andreas Buchmann, Sandro Studer, Antje Saake, Katrin Rauen, Isabelle Zuber, Esmeralda Gruber, Roger M Nitsch, Christoph Hock, Anton Gietl and 1 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
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

19 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Brain-Cognition Fingerprinting via Graph-GCCA with Contrastive Learning.Machine learning in clinical neuroimaging : 7th international workshop, MLCN 2024, held in conjunction with MICCAI 2024, Marrakesh, Morocco, October 10, 2024, proceedings. MLCN (Workshop) (7th : 2024 : Marrakesh, Morocco) · 2025
    Article
  13. Article
  14. Hypertension and cerebral blood flow in the development of Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
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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

11 authors at 1 institution in 1 country.

Dario BachmannInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland. dario.bachmann@irem.uzh.ch.ORCID http://orcid.org/0000-0002-2863-537X
Andreas BuchmannInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Sandro StuderInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Antje SaakeInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Katrin RauenInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Isabelle ZuberInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Esmeralda GruberInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Roger M NitschInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Christoph HockInstitute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Anton Gietl *Institute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.
Valerie Treyer *Institute for Regenerative Medicine, University of Zurich, Schlieren, Switzerland.ORCID http://orcid.org/0000-0002-4584-3031
University of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This work aimed to investigate potential pathways linking age and imaging measures to early age- and pathology-related changes in cognition. We used [18F]-Flutemetamol (amyloid) and [18F]-Flortaucipir (tau) positron emission tomography (PET), structural MRI, and neuropsychological assessment from 232 elderly individuals aged 50-89 years (46.1% women, 23% APOE-ε4 carrier, 23.3% MCI). Tau-PET was available for a subsample of 93 individuals. Structural equation models were used to evaluate cross-sectional pathways between age, amyloid and tau burden, grey matter thickness and volumes, white matter hyperintensity volume, lateral ventricle volume, and cognition. Our results show that age is associated with worse outcomes in most of the measures examined and had similar negative effects on episodic memory and executive functions. While increased lateral ventricle volume was consistently associated with executive function dysfunction, participants with mild cognitive impairment drove associations between structural measures and episodic memory. Both age and amyloid-PET could be associated with medial temporal lobe tau, depending on whether we used a continuous or a dichotomous amyloid variable. Tau burden in entorhinal cortex was related to worse episodic memory in individuals with increased amyloid burden (Centiloid >12) independently of medial temporal lobe atrophy. Testing models for sex differences revealed that amyloid burden was more strongly associated with regional atrophy in women compared with men. These associations were likely mediated by higher tau burden in women. These results indicate that influences of pathological pathways on cognition and sex-specific vulnerabilities are dissociable already in early stages of neuropathology and cognitive impairment.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedAmyloidAmyloid beta-PeptidesAtrophyBrainCognitionCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMalePositron-Emission Tomographytau ProteinsAmyloidAmyloid beta-Peptidestau Proteins

Identifiers

PMID37574523
PMCPMC10423720
OpenAlexW4385792590

What OpenQuestion 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 OpenQuestion graph.