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@ARTICLE{Bauch:278911,
author = {Bauch, Anne and Baur, Julia and Honold, Iris and Willmann,
Matthias and Weber, Greta Louise and Müller, Stephan and
Sodenkamp, Sebastian and Peter, Silke and Schoppmeier,
Ulrich and Laske, Christoph},
title = {{P}rognostic {V}alue of a {M}ultivariate {G}ut {M}icrobiome
{M}odel for {P}rogression from {N}ormal {C}ognition to
{M}ild {C}ognitive {I}mpairment {W}ithin 4 {Y}ears.},
journal = {International journal of molecular sciences},
volume = {26},
number = {10},
issn = {1422-0067},
address = {Basel},
publisher = {Molecular Diversity Preservation International},
reportid = {DZNE-2025-00637},
pages = {4735},
year = {2025},
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.},
keywords = {Humans / Cognitive Dysfunction: microbiology / Cognitive
Dysfunction: diagnosis / Gastrointestinal Microbiome / Male
/ Female / Prognosis / Disease Progression / Aged /
Cognition / Alzheimer Disease: microbiology / ROC Curve /
Middle Aged / Alzheimer’s disease (Other) / gut microbiome
(Other) / longitudinal observational study (Other) / mild
cognitive impairment (Other) / prediction model (Other)},
cin = {AG Gasser / ICRU},
ddc = {540},
cid = {I:(DE-2719)1210000 / I:(DE-2719)1240005},
pnm = {353 - Clinical and Health Care Research (POF4-353) / 899 -
ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-353 / G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40429881},
pmc = {pmc:PMC12112180},
doi = {10.3390/ijms26104735},
url = {https://pub.dzne.de/record/278911},
}