Evidence map›Paper›PMID 40429881›Full record

ArticleInternational journal of molecular sciences2025

Prognostic Value of a Multivariate Gut Microbiome Model for Progression from Normal Cognition to Mild Cognitive Impairment Within 4 Years.

Anne Bauch, Julia Baur, Iris Honold, Matthias Willmann, Greta Louise Weber, Stephan Müller, Sebastian Sodenkamp, Silke Peter, Ulrich Schoppmeier, Christoph Laske

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. Review
  2. Article
  3. Review
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

10 authors.

Anne BauchDepartment of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
Julia BaurDepartment of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
Iris HonoldDepartment of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
Matthias WillmannSYNLAB MVZ Leinfelden-Echterdingen GmbH, Labor Dr. Bayer, 70771 Leinfelden-Echterdingen, Germany.
Greta Louise WeberDepartment of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
Stephan MüllerDepartment of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
Sebastian SodenkampDepartment of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
Silke PeterInstitute of Medical Microbiology and Hygiene, University of Tübingen, 72076 Tübingen, Germany.
Ulrich SchoppmeierInstitute of Medical Microbiology and Hygiene, University of Tübingen, 72076 Tübingen, Germany.ORCID 0009-0004-0769-6845
Christoph LaskeDepartment of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.

Funding

Faber Foundation D3030814Forum Gesundheitsstandort BW 32-5400/58/3University of Tübingen 374-1-0
6 · The paper itself

Abstract

Little is known about the dysbiosis of the gut microbiome in patients with mild cognitive impairment (MCI) potentially at risk for the development of Alzheimer's disease (AD). So far, only cross-sectional differences and not longitudinal changes and their prognostic significance have been in the scope of research in MCI. Therefore, we investigated the ability of longitudinal taxonomic and functional gut microbiome data from 100 healthy controls (HC) to predict the progression from normal cognition to MCI over a 4-year follow-up period (4yFU). Logistic regression models were built with baseline features that best discriminated between the two groups using an ANOVA-type statistical analysis. The best model for the discrimination of MCI converters was based on functional data using Gene Ontology (GO), which included 14 features. This model achieved an area under the receiver operating characteristic curve (AUROC) of 0.84 at baseline, 0.78 at the 1-year follow-up (1yFU), and 0.75 at 4yFU. This functional model outperformed the taxonomic model, which included 38 genera features, in terms of descriptive performance and showed comparable efficacy to combined analyses integrating functional, taxonomic, and clinical characteristics. Thus, gut microbiome algorithms have the potential to predict MCI conversion in HCs over a 4-year period, offering a promising innovative supplement for early AD identification.

Indexed as

CognitionCognitive DysfunctionGastrointestinal MicrobiomeAgedAlzheimer DiseaseDisease ProgressionFemaleHumansMaleMiddle AgedPrognosisROC CurveAlzheimer’s diseasegut microbiomelongitudinal observational studymild cognitive impairmentprediction model

Identifiers

PMID40429881
PMCPMC12112180

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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.