Evidence map›Paper›PMID 40399663›Full record

ReviewCurrent gastroenterology reports2025

Genetic Mutations and Small Bowel Ulcerating Disease: Role in Diagnosis?

Rangesh Modi, Tanner Storozuk, Namrata Setia

Abstract readReview
In one paragraph

Review in Current gastroenterology reports, 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.

Rangesh ModiDepartment of Internal Medicine, Section of Gastroenterology, Hepatology, and Nutrition, University of Chicago, Chicago, IL, 60637, USA.
Tanner StorozukDepartment of Pathology, University of Chicago, 5841 S Maryland Ave, E607, Chicago, IL, 60637, USA.
Namrata SetiaDepartment of Pathology, University of Chicago, 5841 S Maryland Ave, E607, Chicago, IL, 60637, USA. Namrata.Setia@uchicagomedicine.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThis review examines the role of genetic variations in the pathogenesis of small bowel (SB) ulcers associated with Crohn's disease (CD), NSAID enteropathy, and Cryptogenic Multifocal Ulcerous Stenosing Enteritis (CMUSE)/Chronic Non-Specific Ulcers of the Small Intestine (CNSU), aiming to address current diagnostic challenges. RECENT

findingsAdvances in molecular genetics have revealed significant genetic contributors to SB ulceration. In CD, the NOD2 gene on chromosome 16 and several additional risk variants identified through genome-wide association studies (GWAS)-with key insights from the International Inflammatory Bowel Disease Genetics Consortium-have enhanced our understanding of the pathobiology of the disease. In NSAID enteropathy, polymorphisms in CYP enzymes have been associated with altered drug metabolism and gastrointestinal complications. However, the genetic mechanisms underlying deep ulcers in NSAID enteropathy, as well as CMUSE/CNSU, remain poorly understood. Genetic insights are crucial for understanding SB ulcerative diseases. Future research should focus on identifying specific genetic determinants to improve diagnostic accuracy and therapeutic strategies.

Indexed as

Crohn DiseaseIntestinal DiseasesIntestine, SmallMutationUlcerAnti-Inflammatory Agents, Non-SteroidalGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansNod2 Signaling Adaptor ProteinAnti-Inflammatory Agents, Non-SteroidalNOD2 protein, humanNod2 Signaling Adaptor ProteinCMUSECNSUCrohn’s diseaseGeneticsNSAID enteropathyPolymorphismsSmall Bowel Ulcers

Identifiers

PMID40399663
PMCPMC12095398

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Registered trials

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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.