Evidence map›Paper›PMID 40770074›Full record

ArticleCommunications biology2025

Chronological age estimation from human microbiomes with transformer-based Robust Principal Component Analysis.

Tyler Myers, Se Jin Song, Yang Chen, Britta De Pessemier, Lora Khatib, Daniel McDonald, Shi Huang, Richard Gallo, Chris Callewaert, Aki S Havulinna and 7 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

17 authors.

Tyler MyersCenter for Microbiome Innovation, Jacobs School of Engineering, University of California San Diego, La Jolla, CA, USA.
Se Jin SongCenter for Microbiome Innovation, Jacobs School of Engineering, University of California San Diego, La Jolla, CA, USA.
Yang ChenDepartment of Dermatology, University of California San Diego, La Jolla, CA, USA.
Britta De PessemierCenter for Microbial Ecology and Technology, Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0002-3249-176X
Lora KhatibDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Daniel McDonaldDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Shi HuangFaculty of Dentistry, The University of Hong Kong, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-7529-2269
Richard GalloDepartment of Dermatology, University of California San Diego, La Jolla, CA, USA.
Chris CallewaertCenter for Microbial Ecology and Technology, Ghent University, Ghent, Belgium.
Aki S HavulinnaFinnish Institute for Health and Welfare, Helsinki, Finland.ORCID http://orcid.org/0000-0002-4787-8959
Leo LahtiDepartment of Computing, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0001-5537-637X
Guus RoeselersDanone Research and Innovation, Utrecht, the Netherlands.
Manolo LaiolaDanone Research and Innovation, Utrecht, the Netherlands.
Sudarshan A ShettyDanone Research and Innovation, Utrecht, the Netherlands.
Scott T KelleyBioinformatics and Medical Informatics Program, San Diego State University, San Diego, CA, USA.
Rob KnightCenter for Microbiome Innovation, Jacobs School of Engineering, University of California San Diego, La Jolla, CA, USA.
Andrew BartkoCenter for Microbiome Innovation, Jacobs School of Engineering, University of California San Diego, La Jolla, CA, USA. abartko@ucsd.edu.ORCID http://orcid.org/0000-0002-1237-2747

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deep learning for microbiome analysis has shown potential for understanding microbial communities and human phenotypes. Here, we propose an approach, Transformer-based Robust Principal Component Analysis(TRPCA), which leverages the strengths of transformer architectures and interpretability of Robust Principal Component Analysis. To investigate benefits of TRPCA over conventional machine learning models, we benchmarked performance on age prediction from three body sites(skin, oral, gut), with 16S rRNA gene amplicon(16S) and whole-genome sequencing(WGS) data. We demonstrated prediction of age from longitudinal samples and combined classification and regression tasks via multi-task learning(MTL). TRPCA improves age prediction accuracy from human microbiome samples, achieving the largest reduction in Mean Absolute Error for WGS skin (MAE: 8.03, 28% reduction) and 16S skin (MAE: 5.09, 14% reduction) samples, compared to conventional approaches. Additionally, TRPCA's MTL approach achieves an accuracy of 89% for birth country prediction across 5 countries, while improving age prediction from WGS stool samples. Notably, TRPCA uncovers a link between subject and error prediction through residual analysis for paired samples across sequencing method (16S/WGS) and body site(oral/gut). These findings highlight TRPCA's utility in improving age prediction while maintaining feature-level interpretability, and elucidating connections between individuals and microbiomes.

Indexed as

AgingBiometryDeep LearningGastrointestinal MicrobiomePrincipal Component AnalysisSkin MicrobiomeHumansSoftware Validation

Identifiers

PMID40770074
PMCPMC12328700

What Socratic 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 Socratic graph.