Evidence map›Paper›PMID 39605360›Full record

ArticlebioRxiv : the preprint server for biology2024

Longitudinal Microbiome-based Interpretable Machine Learning for Identification of Time-Varying Biomarkers in Early Prediction of Disease Outcomes.

Yifan Dai, Yunzhi Qian, Yixiang Qu, Wyliena Guan, Jialiu Xie, Duan Wang, Catherine Butler, Stuart Dashper, Ian Carroll, Kimon Divaris and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Yifan DaiDepartment of Biostatistics, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.
Yunzhi QianDepartment of Nutrition, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.
Yixiang QuDepartment of Biostatistics, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.
Wyliena GuanDepartment of Biostatistics, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.
Jialiu XieDepartment of Biostatistics, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.
Duan WangNorth Carolina School of Science and Mathematics.
Catherine ButlerMelbourne Dental School, University of Melbourne.
Stuart DashperMelbourne Dental School, University of Melbourne.
Ian CarrollDepartment of Nutrition, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.
Kimon DivarisDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina at Chapel Hill.
Yufeng LiuDepartment of Biostatistics, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.
Di WuDepartment of Biostatistics, Gillings School of Global Public Health at University of North Carolina at Chapel Hill.ORCID 0000-0001-8331-2357

Funding

Genome-Wide Association Study of Early Childhood CariesU01DE025046 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DIVARIS, KIMON · 2015 to 2019
$8.4M
Investigating the microbial basis of early childhood caries via integrative analysis of metagenomics metatranscriptomics and metabolomicsR03DE034507 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WU, DI · 2024 to 2025
$297k
NIDCR NIH HHS R03 DE034507NIDCR NIH HHS U01 DE025046
6 · The paper itself

Abstract

Information generated from longitudinally-sampled microbial data has the potential to illuminate important aspects of development and progression for many human conditions and diseases. Identifying microbial biomarkers and their time-varying effects can not only advance our understanding of pathogenetic mechanisms, but also facilitate early diagnosis and guide optimal timing of interventions. However, longitudinal predictive modeling of highly noisy and dynamic microbial data (e.g., metagenomics) poses analytical challenges. To overcome these challenges, we introduce a robust and interpretable machine-learning-based longitudinal microbiome analysis framework, LP-Micro, that encompasses: (i) longitudinal microbial feature screening via a polynomial group lasso, (ii) disease outcome prediction implemented via machine learning methods (e.g., XGBoost, deep neural networks), and (iii) interpretable association testing between time points, microbial features, and disease outcomes via permutation feature importance. We demonstrate in simulations that LP-Micro can not only identify incident disease-related microbiome taxa but also offers improved prediction accuracy compared to existing approaches. Applications of LP-Micro in two longitudinal microbiome studies with clinical outcomes of childhood dental disease and weight loss following bariatric surgery yield consistently high prediction accuracy. The identified critical early predictive time points are informative and aligned with clinical expectations.

Identifiers

PMID39605360
PMCPMC11601495

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.