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PRJEB85717 ERP169091

Gut microbiome prediction of MCI conversion in German elderly

Prognostic value of gut microbiome for progression from normal cognition to mild cognitive impairment within 4 years

1 sample from a healthy elderly control in Germany, part of a longitudinal study of 100 healthy controls tracking gut microbiome changes predictive of progression from normal cognition to mild cognitive impairment over 4 years. machine-written summary

1 samples · 1 runs · DE · Age unknown · 2025 · 3.45 Gbp / sample

Sources
✓Sequence archive 1✓Abstract / description 2✓Full text 2○Supplementary tables–External resources–User contribution–Human verified

Checked this project's papers and archive records yourself? Mark it human-verified.

what each source gave
✓ Sequence archive1 sample values (country)
✓ Abstract / description2 sample values (health condition, health condition detail)
✓ Full text2 sample values (collection date, location site) · PMC12112180
○ Supplementary tablesfiles read; no table could be matched to the samples
– External resourcesnot covered by the external resources we ingest
– User contributionnothing uploaded yet
– Human verifiednot yet checked by a person · I checked this project — verify it
Samples at a glance
1 country
Age
elderly1
Condition
healthy_control1
Country
DE1
Body site
primary1
Sequencing depth per sample · this project all projects
all projects, 0–0.03 Gbp: 25,080 samples (4 %)all projects, 0.03–0.1 Gbp: 17,066 samples (3 %)all projects, 0.1–0.3 Gbp: 29,179 samples (5 %)all projects, 0.3–1 Gbp: 47,044 samples (8 %)all projects, 1–3 Gbp: 124,983 samples (22 %)all projects, 3–10 Gbp: 253,728 samples (44 %)this project, 3–10 Gbp: 1 samplesall projects, 10–30 Gbp: 72,533 samples (13 %)all projects, 30–100 Gbp: 3,024 samples (1 %)all projects, 100–300 Gbp: 106 samples (0 %)all projects, ≥ 300 Gbp: 9 samples (0 %)project median 3.45 Gbp per sample0130Gbp
Sampling design and relatedness

longitudinal — not resolved

Schedule stated by the source: “Same healthy controls sampled at baseline, 1-year follow-up (1yFU), and 4-year follow-up (4yFU)” (time origin: baseline/enrolment); stated follow-up 4.0 y.

How longitudinal and relatedness information is derived

Community composition

No Sandpiper profile for this project's samples yet.

Field coverage
fieldsamplescoverageR1R2R3R4
age_category1 100%
country1 100%1
health_condition1 100%1
subject_id0 0%
collection_date1 100%1
detailed_location1 100%
health_condition_detail1 100%1
location_site1 100%1
Papers (1)
  • Prognostic Value of a Multivariate Gut Microbiome Model for Progression from Normal Cognition to Mild Cognitive Impairment Within 4 Years. 2025 PMID 40429881 PMC12112180 own_data
Details
Archive description

Dysbiosis of the gut microbiome has been linked to the pathogenesis of Alzheimer`s disease (AD). How-ever, little is known about the longitudinal changes in the gut microbiome and its prognostic significance in early stages of AD, particularly in healthy individuals (HCs) who later develop mild cognitive impair-ment (MCI). Therefore, we investigated the ability of taxonomic and functional gut microbiome data from 100 HCs 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 statistic. 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 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 anal-yses integrating functional, taxonomic, and clinical characteristics. 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 prognosis.

How this project entered the registry

Classified as human gut / stool shotgun DNA metagenome of age unknown by sonnet_x2 with confidence 0.62. Assay shotgun_dna.

  • host run.scientific_name · “Homo sapiens”
  • body site study.title · “Prognostic value of gut microbiome”
Evidence examples (one per field × route)
samplefieldvaluerouteconf.sourcequote
SAMEA118775003collection_date2016/2018R30.70paper.fulltext.methodsTübingen (Germany) starting from 2016 to end of 2018
SAMEA118775003countryDER10.90sample.attr.geographic_location_country_and_or_seaGermany
SAMEA118775003health_conditionhealthy_controlR40.50paper.abstract100 healthy controls (HC)
SAMEA118775003health_condition_detailHealthy controls at baseline; longitudinal follow-up for MCI progressionR40.50paper.abstract100 healthy controls (HC)
SAMEA118775003location_siteSection of Dementia Research, Department of Psychiatry and Psychotherapy, TübingenR30.70paper.fulltext.methodsrecruited at the Section of Dementia Research at the Department of Psychiatry
Sequencing

1 runs over 1 samples · mean 3.45 Gbp per run (median 3.45 Gbp, total 3.45 Gbp; 1 runs with a base count) · layout PAIRED 1 · platform ILLUMINA 1 · models unspecified (1) · 0% of runs with a Sandpiper profile · first public 2025-07-30

Authors (10)

Bauch A first · Baur J · Honold I · Willmann M · Weber GL · Müller S · Sodenkamp S · Peter S · Schoppmeier U · Laske C last

Downloads

PRJEB85717.csv.gz (989 B) · parquet (70.2 KB) — all 1 samples, every field with route and confidence · PRJEB85717_determinations.csv.gz (717 B) — 5 evidence rows

Samples (1 · every field this project has values for · hover a cell for its source)
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