Evidence map›Paper›PMID 33741501›Full record

ArticleCellular and molecular gastroenterology and hepatology2021

Lack of Mucosal Cholinergic Innervation Is Associated With Increased Risk of Enterocolitis in Hirschsprung's Disease.

Simone Keck, Virginie Galati-Fournier, Urs Kym, Michèle Moesch, Jakob Usemann, Isabelle Müller, Ulrike Subotic, Sasha J Tharakan, Thomas Krebs, Eleuthere Stathopoulos and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 35 citations in OpenAlex.

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  15. Hirschsprung-associated enterocolitis: a comprehensive review.World journal of pediatric surgery · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 8 institutions in 2 countries.

Simone KeckDepartment of Pediatric Surgery, University Children's Hospital Basel (UKBB) and University of Basel, Basel, Switzerland. Electronic address: simone.keck@unibas.ch.
Virginie Galati-FournierDepartment of Pediatric Surgery, University Children's Hospital Basel (UKBB) and University of Basel, Basel, Switzerland.
Urs KymDepartment of Pediatric Surgery, University Children's Hospital Basel (UKBB) and University of Basel, Basel, Switzerland.
Michèle MoeschDepartment of Pediatric Surgery, University Children's Hospital Basel (UKBB) and University of Basel, Basel, Switzerland.
Jakob UsemannDepartment of Pediatric Pulmonology, University Children's Hospital Basel (UKBB), Basel, and Division of Respiratory Medicine, University Children's Hospital Zurich, Zurich, Switzerland.
Isabelle MüllerDepartment of Pediatric Surgery, University Children's Hospital Basel (UKBB) and University of Basel, Basel, Switzerland.
Ulrike SuboticDepartment of Pediatric Surgery, University Children's Hospital Basel (UKBB) and University of Basel, Basel, Switzerland; Department of Pediatric Surgery, University Children's Hospital Zurich, Zurich, Switzerland.
Sasha J TharakanDepartment of Pediatric Surgery, University Children's Hospital Zurich, Zurich, Switzerland.
Thomas KrebsDepartment of Pediatric Surgery, Children's Hospital of Eastern Switzerland, St Gallen, Switzerland.
Eleuthere StathopoulosDepartment of Pediatric Surgery, University Hospital of Lausanne (CHUV), Lausanne, Switzerland.
Peter SchmittenbecherDepartment of Pediatric Surgery, Municipal Hospital, Karlsruhe, Germany.
Dietmar CholewaDepartment of Pediatric Surgery, University Hospital of Bern, Bern, Switzerland.
Philipp RomeroDepartment of Pediatric Surgery, University Hospital of Heidelberg, Heidelberg, Germany.
Bertram ReingruberDepartment of Pediatric Surgery, Florence Nightingale Hospital, Düsseldorf, Germany.
Elisabeth BruderInstitute for Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
Nig Study GroupNIG Study Group, Lausanne, Switzerland; Department of Pathology, University Hospital of Lausanne (CHUV) and University of Lausanne, Lausanne, Switzerland.
Stefan Holland-CunzDepartment of Pediatric Surgery, University Children's Hospital Basel (UKBB) and University of Basel, Basel, Switzerland.
University of Basel · CHUniversity Hospital of Lausanne · CHHeidelberg University · DEStädtisches Klinikum Karlsruhe · DEUniversity Children’s Hospital Basel · CHUniversity Children's Hospital Zurich · CHUniversity Hospital of Basel · CHUniversity Hospital of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsHirschsprung's disease (HSCR) is a congenital intestinal motility disorder defined by the absence of enteric neuronal cells (ganglia) in the distal gut. The development of HSCR-associated enterocolitis remains a life-threatening complication. Absence of enteric ganglia implicates innervation of acetylcholine-secreting (cholinergic) nerve fibers. Cholinergic signals have been reported to control excessive inflammation, but the impact on HSCR-associated enterocolitis is unknown.

methodsWe enrolled 44 HSCR patients in a prospective multicenter study and grouped them according to their degree of colonic mucosal acetylcholinesterase-positive innervation into low-fiber and high-fiber patient groups. The fiber phenotype was correlated with the tissue cytokine profile as well as immune cell frequencies using Luminex analysis and fluorescence-activated cell sorting analysis of colonic tissue and immune cells. Using confocal immunofluorescence microscopy, macrophages were identified in close proximity to nerve fibers and characterized by RNA-seq analysis. Microbial dysbiosis was analyzed in colonic tissue using 16S-rDNA gene sequencing. Finally, the fiber phenotype was correlated with postoperative enterocolitis manifestation.

resultsThe presence of mucosal nerve fiber innervation correlated with reduced T-helper 17 cytokines and cell frequencies. In high-fiber tissue, macrophages co-localized with nerve fibers and expressed significantly less interleukin 23 than macrophages from low-fiber tissue. HSCR patients lacking mucosal nerve fibers showed microbial dysbiosis and had a higher incidence of postoperative enterocolitis.

conclusionsThe mucosal fiber phenotype might serve as a prognostic marker for enterocolitis development in HSCR patients and may offer an approach to personalized patient care and new therapeutic options.

Indexed as

AcetylcholinesteraseChildChild, PreschoolCholinergic NeuronsCohort StudiesCytokinesDysbiosisEnterocolitisEpithelial CellsFemaleHirschsprung DiseaseHumansInfantInfant, NewbornInflammationIntestinal MucosaAcetylcholinesteraseCytokinesLipopolysaccharide ReceptorsRNA, MessengerCholinergic Nerve FibersEnterocolitisMacrophagesMicrobiomeNeuroimmunologyTh17 Cells

Identifiers

PMID33741501
PMCPMC8258990
OpenAlexW3138460962

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.