Evidence map›Paper›PMID 39499254›Full record

ReviewAmerican journal of physiology. Gastrointestinal and liver physiology2025

Early subclinical stages of the inflammatory bowel diseases: insights from human and animal studies.

Cecelia Kelly, R Balfour Sartor, John F Rawls

Abstract readReview
In one paragraph

Review in American journal of physiology. Gastrointestinal and liver physiology, 2025. 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. Article
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

3 authors.

Cecelia KellyDepartment of Molecular Genetics and Microbiology, Duke Microbiome Center, Duke University School of Medicine, Durham, North Carolina, United States.ORCID 0000-0001-6105-5492
R Balfour SartorDivision of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina, Chapel Hill, North Carolina, United States.
John F RawlsDepartment of Molecular Genetics and Microbiology, Duke Microbiome Center, Duke University School of Medicine, Durham, North Carolina, United States.ORCID 0000-0002-5976-5206

Funding

PILOT AND FEASIBILITY STUDIESP30DK034987 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROBERT S. SANDLER · 1985 to 2026
$30.5M
Role of IL-10 in APC Regulation of Protective vs. Pathogenic T Cell Responses toP01DK094779 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SARTOR, RYAN B · 2013 to 2023
$17.9M
Genetic determinants of Bacteroides vulgatus colonization fitness and host inflammatory responsesR01DK136231 · NIDDK · DUKE UNIVERSITY · PI John F Rawls · 2023 to 2026
$2.6M
Microbial regulation of intestinal epithelial gene expressionR01DK141168 · NIDDK · DUKE UNIVERSITY · PI John F Rawls · 2024 to 2026
$2.0M
The role of HNF4a in maintaining intestinal epithelial cell homeostasis in the presence of microbesF31DK121392 · NIDDK · DUKE UNIVERSITY · PI KELLY, CECELIA · 2020 to 2022
$114k
HHS | National Institutes of Health (NIH) F31-DK121392HHS | National Institutes of Health (NIH) P01-DK094779HHS | National Institutes of Health (NIH) P30-DK034987HHS | National Institutes of Health (NIH) R01-DK136231NIDDK NIH HHS F31 DK121392NIDDK NIH HHS P01 DK094779NIDDK NIH HHS P30 DK034987NIDDK NIH HHS R01 DK136231NIDDK NIH HHS R01 DK141168
6 · The paper itself

Abstract

The inflammatory bowel diseases (IBD) occur in genetically susceptible individuals that mount inappropriate immune responses to their microbiota leading to chronic intestinal inflammation. The natural history of IBD progression begins with early subclinical stages of disease that occur before clinical diagnosis. Improved understanding of those early subclinical stages could lead to new or improved strategies for IBD diagnosis, prognostication, or prevention. Here, we review our current understanding of the early subclinical stages of IBD in humans including studies from first-degree relatives of patients with IBD and members of the general population who go on to develop IBD. We also discuss representative mouse models of IBD that can be used to investigate disease dynamics and host-microbiota relationships during these early stages. In particular, we underscore how mouse models of IBD that develop disease later in life with variable penetrance may present valuable opportunities to discern early subclinical mechanisms of disease before histological inflammation and other severe symptoms become apparent.

Indexed as

Disease Models, AnimalGastrointestinal MicrobiomeInflammatory Bowel DiseasesAnimalsDisease ProgressionHumansMicecolitisIBDpediatricpreclinicalsubclinical

Identifiers

PMID39499254
PMCPMC11901386

What OpenQuestion holds

Textmetadata
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.