Evidence map›Paper›PMID 35932029›Full record

ArticleMicrobiome2022

Microbial risk score for capturing microbial characteristics, integrating multi-omics data, and predicting disease risk.

Chan Wang, Leopoldo N Segal, Jiyuan Hu, Boyan Zhou, Richard B Hayes, Jiyoung Ahn, Huilin Li

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Microbiome, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% of its field
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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  9. Design, processing, and modeling for longitudinal multiomics microbiome data.Frontiers in cellular and infection microbiology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Chan WangDivision of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Leopoldo N SegalDivision of Pulmonary and Critical Care Medicine, New York University Grossman School of Medicine, New York, NY, 10017, USA.
Jiyuan HuDivision of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Boyan ZhouDivision of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Richard B HayesDivision of Epidemiology, Department of Population Health, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Jiyoung AhnDivision of Epidemiology, Department of Population Health, New York University Grossman School of Medicine, New York, NY, 10016, USA.
Huilin LiDivision of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, NY, 10016, USA. Huilin.Li@nyulangone.org.
New York University · US

Funding

Local microbiota signatures of pro-tumor immunity and checkpoint inhibition susceptibility in lung cancerR37CA244775 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Leopoldo Nicolas Segal · 2020 to 2026
$4.7M
The Oral Microbiome and Upper Aerodigestive Squamous Cell CancerR01CA159036 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG, HAYES, RICHARD BERNARD · 2011 to 2024
$3.5M
Project 2P20CA252728 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG · 2020 to 2022
$3.4M
NCI NIH HHS P20 CA252728NCI NIH HHS R01 CA159036NCI NIH HHS R37 CA244775
6 · The paper itself

Abstract

backgroundWith the rapid accumulation of microbiome-wide association studies, a great amount of microbiome data are available to study the microbiome's role in human disease and advance the microbiome's potential use for disease prediction. However, the unique features of microbiome data hinder its utility for disease prediction.

methodsMotivated from the polygenic risk score framework, we propose a microbial risk score (MRS) framework to aggregate the complicated microbial profile into a summarized risk score that can be used to measure and predict disease susceptibility. Specifically, the MRS algorithm involves two steps: (1) identifying a sub-community consisting of the signature microbial taxa associated with disease and (2) integrating the identified microbial taxa into a continuous score. The first step is carried out using the existing sophisticated microbial association tests and pruning and thresholding method in the discovery samples. The second step constructs a community-based MRS by calculating alpha diversity on the identified sub-community in the validation samples. Moreover, we propose a multi-omics data integration method by jointly modeling the proposed MRS and other risk scores constructed from other omics data in disease prediction.

resultsThrough three comprehensive real-data analyses using the NYU Langone Health COVID-19 cohort, the gut microbiome health index (GMHI) multi-study cohort, and a large type 1 diabetes cohort separately, we exhibit and evaluate the utility of the proposed MRS framework for disease prediction and multi-omics data integration. In addition, the disease-specific MRSs for colorectal adenoma, colorectal cancer, Crohn's disease, and rheumatoid arthritis based on the relative abundances of 5, 6, 12, and 6 microbial taxa, respectively, are created and validated using the GMHI multi-study cohort. Especially, Crohn's disease MRS achieves AUCs of 0.88 (0.85-0.91) and 0.86 (0.78-0.95) in the discovery and validation cohorts, respectively.

conclusionsThe proposed MRS framework sheds light on the utility of the microbiome data for disease prediction and multi-omics integration and provides a great potential in understanding the microbiome's role in disease diagnosis and prognosis. Video Abstract.

Indexed as

COVID-19Crohn DiseaseMicrobiotaDisease SusceptibilityHumansRisk FactorsAlpha diversityDisease predictionMicrobial risk scoreMicrobiome-wide association studiesMulti-omics data integrationSub-community

Identifiers

PMID35932029
PMCPMC9354433
OpenAlexW4289866413

What OpenQuestion 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 OpenQuestion graph.