Evidence map›Paper›PMID 41220286›Full record

ReviewGut and liver2026

Translating Gut Microbiota into Diagnostics: A Multidimensional Approach for the Diagnosis of Inflammatory Bowel Disease.

June-Young Lee, Ji-Ho Yoo, Ji Eun Kim, Jin-Woo Bae, Chang Kyun Lee

Abstract readReview
In one paragraph

Review in Gut and liver, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

5 authors.

June-Young LeeDepartment of Biology, Kyung Hee University, Seoul, Korea.ORCID 0000-0002-6793-6108
Ji-Ho YooDepartment of Biomedical and Pharmaceutical Sciences, Kyung Hee University, Seoul, Korea.ORCID 0000-0001-5507-3707
Ji Eun KimDepartment of Gastroenterology, Center for Crohn's and Colitis, Kyung Hee University Hospital, College of Medicine, Kyung Hee University, Seoul, Korea.ORCID 0009-0003-9877-6543
Jin-Woo BaeDepartment of Biology, Kyung Hee University, Seoul, Korea.ORCID 0000-0001-6433-5270
Chang Kyun LeeDepartment of Gastroenterology, Center for Crohn's and Colitis, Kyung Hee University Hospital, College of Medicine, Kyung Hee University, Seoul, Korea.ORCID 0000-0002-4279-3825

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiota has emerged as a key factor in the pathophysiology of inflammatory bowel disease (IBD), providing novel opportunities for diagnostic innovation. Traditional biomarkers, such as C-reactive protein and fecal calprotectin, are widely used in clinical practice; however, their ability to reflect disease complexity and microbial dysregulation remains limited. Recent advances in metagenomics and multi-omics integration have enabled high-resolution profiling of microbial communities and their functional capacities and associated metabolites. Differential abundance analysis and machine learning models have been used to identify microbial biomarkers that can distinguish patients with IBD from healthy individuals. Multicohort studies integrating microbiome and metabolomic data have further improved diagnostic accuracy and generalizability. Transcriptomic and proteomic analyses provide complementary insights into host-microbe interactions and disease mechanisms. In this review, we explored the potential of metagenomic biodata as diagnostic markers for IBD, with an emphasis on a multidimensional analytical approach. We highlight the recent developments in sequencing technologies, computational pipelines for microbial feature selection, and machine learning strategies applied to biomarker discovery. The integration of multi-omics data deepens our understanding of host-microbe interactions and facilitates the development of microbiota-informed diagnostic tools. As multidimensional microbial profiling evolves, its clinical utility for the diagnosis and stratification of IBD requires further investigation.

Indexed as

Gastrointestinal MicrobiomeInflammatory Bowel DiseasesBiomarkersFecesHumansMachine LearningMetabolomicsMetagenomicsProteomicsBiomarkersBiomarkersGastrointestinal microbiomeInflammatory bowel diseasesMetagenomicsMultiomics

Identifiers

PMID41220286
PMCPMC12989658

What Socratic 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 Socratic graph.