Evidence map›Paper›PMID 26801768›Full record

ArticleBMC medical genomics2016

Gene expression profiling in necrotizing enterocolitis reveals pathways common to those reported in Crohn's disease.

Éric Tremblay, Marie-Pier Thibault, Emanuela Ferretti, Corentin Babakissa, Valérie Bertelle, Marcos Bettolli, Karolina Maria Burghardt, Jean-François Colombani, David Grynspan, Emile Levy and 7 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC medical genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.9field-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

30 citing papers in PubMed, 53 citations in OpenAlex.

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  8. Elevated DUOX2 levels correlate with necrotizing enterocolitis development.Frontiers in cellular and infection microbiology · 2025
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  20. Necrotizing Enterocolitis: Overview on In Vitro Models.International journal of molecular sciences · 2021
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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

17 authors at 9 institutions in 4 countries.

Éric TremblayDepartment of Anatomy and Cell Biology, Faculté de Médecine et Sciences de la Santé, Université de Sherbrooke, 3001, 12th Avec North, J1H 5N4, Sherbrooke, QC, Canada. eric.tremblay@usherbrooke.ca.
Marie-Pier ThibaultDepartment of Anatomy and Cell Biology, Faculté de Médecine et Sciences de la Santé, Université de Sherbrooke, 3001, 12th Avec North, J1H 5N4, Sherbrooke, QC, Canada. marie-pier.thibault@usherbrooke.ca.
Emanuela FerrettiDivision of Neonatology, Department of Pediatrics, CHEO, Ottawa, ON, Canada. eferretti@toh.ca.
Corentin BabakissaDepartment of Pediatrics, Faculté de Médecine et Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada. corentin.babakissa@usherbrooke.ca.
Valérie BertelleDivision of Neonatology, Department of Pediatrics, Faculté de Médecine et Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada. valerie.bertelle@usherbrooke.ca.
Marcos BettolliDepartment of Surgery, CHEO, Ottawa, ON, Canada. mbettolli@cheo.on.ca.
Karolina Maria BurghardtDivision of Gastroenterology, Hepatology & Nutrition, CHEO, Ottawa, ON, Canada. karolina.burghardt@gmail.com.
Jean-François ColombaniDepartment of Pediatrics, CHU de Martinique, Fort-de-France, France. jean-francois.colombani@chu-fortdefrance.fr.
David GrynspanDepartment of Pathology and Laboratory Medicine, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada. dgrynspan@cheo.on.ca.
Emile LevyDepartment of Nutrition, Centre de recherche, CHU Sainte-Justine, Université de Montréal, Montréal, QC, Canada. emile.levy@recherche-ste-justine.qc.ca.
Peng LuDepartment of Pediatrics, Erasmus MC-Sophia, Rotterdam, The Netherland. pengluerasmusmc@gmail.com.
Sandeep MayerDepartment of Surgery, Faculté de Médecine et Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada. sandeep.mayer@usherbrooke.ca.
Daniel MénardDepartment of Anatomy and Cell Biology, Faculté de Médecine et Sciences de la Santé, Université de Sherbrooke, 3001, 12th Avec North, J1H 5N4, Sherbrooke, QC, Canada. daniel.menard@usherbrooke.ca.
Olivier MouterdeCHU de Rouen, Department of Medical Pediatrics, Rouen, France. olivier.mouterde@chu-rouen.fr.
Ingrid B RenesDepartment of Pediatrics, Erasmus MC-Sophia, Rotterdam, The Netherland. i.b.renes@amc.uva.nl.
Ernest G SeidmanDivision of Gastroenterology, McGill University, Montréal, QC, Canada. digestivelab@hotmail.com.
Jean-François BeaulieuDepartment of Anatomy and Cell Biology, Faculté de Médecine et Sciences de la Santé, Université de Sherbrooke, 3001, 12th Avec North, J1H 5N4, Sherbrooke, QC, Canada. jean-francois.beaulieu@usherbrooke.ca.
Université de Sherbrooke · CAErasmus MC - Sophia Children’s Hospital · NLAgricultural Research Institute of Ontario · CACanadian Nutrition Society · CACentre Hospitalier Universitaire de Martinique · MQCentre Hospitalier Universitaire de Rouen · FRCentre Hospitalier Universitaire Sainte-Justine · CAMcGill University · CAUniversity of Ottawa · CA

Funding

Canadian Institutes of Health Research MOP 136991
6 · The paper itself

Abstract

backgroundNecrotizing enterocolitis (NEC) is the most frequent life-threatening gastrointestinal disease experienced by premature infants in neonatal intensive care units. The challenge for neonatologists is to detect early clinical manifestations of NEC. One strategy would be to identify specific markers that could be used as early diagnostic tools to identify preterm infants most at risk of developing NEC or in the event of a diagnostic dilemma of suspected disease. As a first step in this direction, we sought to determine the specific gene expression profile of NEC.

methodsDeep sequencing (RNA-Seq) was used to establish the gene expression profiles in ileal samples obtained from preterm infants diagnosed with NEC and non-NEC conditions. Data were analyzed with Ingenuity Pathway Analysis and ToppCluster softwares.

resultsData analysis indicated that the most significant functional pathways over-represented in NEC neonates were associated with immune functions, such as altered T and B cell signaling, B cell development, and the role of pattern recognition receptors for bacteria and viruses. Among the genes that were strongly modulated in neonates with NEC, we observed a significant degree of similarity when compared with those reported in Crohn's disease, a chronic inflammatory bowel disease.

conclusionsGene expression profile analysis revealed a predominantly altered immune response in the intestine of NEC neonates. Moreover, comparative analysis between NEC and Crohn's disease gene expression repertoires revealed a surprisingly high degree of similarity between these two conditions suggesting a new avenue for identifying NEC biomarkers.

Indexed as

Gene Expression ProfilingAntiviral AgentsCrohn DiseaseEnterocolitis, NecrotizingFemaleHumansImmunity, InnateInfant, NewbornMalePregnancyReproducibility of ResultsSequence Analysis, RNASignal TransductionAntiviral Agents

Identifiers

PMID26801768
PMCPMC4722613
OpenAlexW2265376827

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.