Evidence map›Paper›PMID 36503356›Full record

ReviewGut microbes

Stool multi-omics for the study of host-microbe interactions in inflammatory bowel disease.

Consuelo Sauceda, Charlie Bayne, Khadijeh Sudqi, Antonio Gonzalez, Parambir S Dulai, Rob Knight, David J Gonzalez, Carlos G Gonzalez

Open access · goldAbstract readReview
In one paragraph

Review in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Consuelo SaucedaDepartment of Pharmacology, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-1487-6631
Charlie BayneDepartment of Pharmacology, University of California San Diego, La Jolla, CA, USA.
Khadijeh SudqiDepartment of Pharmacology, University of California San Diego, La Jolla, CA, USA.
Antonio GonzalezDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Parambir S DulaiDivision of Gastroenterology and Hepatology, Northwestern University, Chicago, IL, USA.
Rob KnightCenter for Microbiome Innovation, University of California San Diego, La Jolla, CA, USA.
David J GonzalezDepartment of Pharmacology, University of California San Diego, La Jolla, CA, USA.
Carlos G GonzalezDepartment of Pharmacology, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-4673-4048
University of California San Diego · USNorthwestern University · US

Funding

GRADUATE TRAINING IN CELLULAR &MOLECULAR PHARMACOLOGYT32GM007752 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER, HANDEL, TRACY M · 1985 to 2023
$13.5M
San Diego Digestive Diseases Research CenterP30DK120515 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Bernd G. Schnabl · 2019 to 2026
$10.8M
Training Grant in GastroenterologyT32DK007202 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GHOSH, PRADIPTA · 1985 to 2022
$7.7M
Microbiome Driven Proteolysis as a Contributing Factor to Severity of Ulcerative Colitis Disease ActivityR01DK131005 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GONZALEZ, DAVID J · 2022 to 2024
$1.6M
Hyperbaric Oxygen Therapy for Ulcerative Colitis Patients Hospitalized for Moderate to Severe Flares: A Multi-Center, Randomized, Double-Blind, Sham Controlled Trial (HBOT-UC)U34DK126626 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DULAI, PARAMBIR SINGH · 2021 to 2021
$347k
NIDDK NIH HHS P30 DK120515NIDDK NIH HHS R01 DK131005NIDDK NIH HHS T32 DK007202NIDDK NIH HHS U34 DK126626NIGMS NIH HHS T32 GM007752
6 · The paper itself

Abstract

Inflammatory Bowel Disease (IBD) is a chronic immune-mediated inflammatory disease of the gastrointestinal tract that is a growing public burden. Gut microbes and their interactions with hosts play a crucial role in disease pathogenesis and progression. These interactions are complex, spanning multiple physiological systems and data types, making comprehensive disease assessment difficult, and often overwhelming single-omic capabilities. Stool-based multi-omics is a promising approach for characterizing host-gut microbiome interactions using deep integration of technologies such as 16S rRNA sequencing, shotgun metagenomics, meta-transcriptomics, metabolomics, and metaproteomics. The wealth of information generated through multi-omic studies is poised to usher in advancements in IBD research and precision medicine. This review highlights historical and recent findings from stool-based muti-omic studies that have contributed to unraveling IBD's complexity. Finally, we discuss common pitfalls, issues, and limitations, and how future pipelines should address them to standardize multi-omics in IBD research and beyond.

Indexed as

Gastrointestinal MicrobiomeInflammatory Bowel DiseasesHost Microbial InteractionsHumansMultiomicsRNA, Ribosomal, 16SRNA, Ribosomal, 16Sdietgut microbesInflammatory bowel disease (IBD)metabolomicsmetagenomicsmetaproteomicsMulti-omicsprecision medicine

Identifiers

PMID36503356
PMCPMC9746627
OpenAlexW4311125304

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.