Evidence map›Paper›PMID 33806322›Full record

ArticleInternational journal of molecular sciences2021

Deciphering the Transcriptomic Heterogeneity of Duodenal Coeliac Disease Biopsies.

Johannes Wolf, Edith Willscher, Henry Loeffler-Wirth, Maria Schmidt, Gunter Flemming, Marlen Zurek, Holm H Uhlig, Norman Händel, Hans Binder

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  9. Celiac disease: From genetics to epigenetics.World journal of gastroenterology · 2022
    Review
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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

9 authors at 4 institutions in 2 countries.

Johannes WolfDepartment of Laboratory Medicine at Hospital "St. Georg" Leipzig, 04129 Leipzig, Germany.
Edith WillscherIZBI, Interdisciplinary Centre for Bioinformatics, University Leipzig, Härtelstr. 16-18, 04107 Leipzig, Germany.
Henry Loeffler-WirthIZBI, Interdisciplinary Centre for Bioinformatics, University Leipzig, Härtelstr. 16-18, 04107 Leipzig, Germany.
Maria SchmidtIZBI, Interdisciplinary Centre for Bioinformatics, University Leipzig, Härtelstr. 16-18, 04107 Leipzig, Germany.ORCID 0000-0002-5317-3920
Gunter FlemmingPaediatric Gastroenterology Unit, University Hospital for Children and Adolescents, 04103 Leipzig, Germany.
Marlen ZurekChildren's Hospital of the Clinical Centre "Sankt Georg", 04129 Leipzig, Germany.
Holm H UhligTranslational Gastroenterology Unit, Oxford NIHR Biomedical Research Centre, Experimental Medicine, Department of Paediatrics, University of Oxford, John Radcliffe Hospital, Oxford OX4 2PG, UK.ORCID 0000-0002-6111-7355
Norman HändelChildren's Hospital of the Clinical Centre "Sankt Georg", 04129 Leipzig, Germany.
Hans BinderIZBI, Interdisciplinary Centre for Bioinformatics, University Leipzig, Härtelstr. 16-18, 04107 Leipzig, Germany.ORCID 0000-0002-2242-4678
Leipzig University · DEKlinikum St. Georg · DEJohn Radcliffe Hospital · GBUniversity Hospital Leipzig · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coeliac disease (CD) is a clinically heterogeneous autoimmune disease with variable presentation and progression triggered by gluten intake. Molecular or genetic factors contribute to disease heterogeneity, but the reasons for different outcomes are poorly understood. Transcriptome studies of tissue biopsies from CD patients are scarce. Here, we present a high-resolution analysis of the transcriptomes extracted from duodenal biopsies of 24 children and adolescents with active CD and 21 individuals without CD but with intestinal afflictions as controls. The transcriptomes of CD patients divide into three groups-a mixed group presenting the control cases, and CD-low and CD-high groups referring to lower and higher levels of CD severity. Persistence of symptoms was weakly associated with subgroup, but the highest marsh stages were present in subgroup CD-high, together with the highest cell cycle rates as an indicator of virtually complete villous atrophy. Considerable variation in inflammation-level between subgroups was further deciphered into immune cell types using cell type de-convolution. Self-organizing maps portrayal was applied to provide high-resolution landscapes of the CD-transcriptome. We find asymmetric patterns of miRNA and long non-coding RNA and discuss the effect of epigenetic regulation. Expression of genes involved in interferon gamma signaling represent suitable markers to distinguish CD from non-CD cases. Multiple pathways overlay in CD biopsies in different ways, giving rise to heterogeneous transcriptional patterns, which potentially provide information about etiology and the course of the disease.

Indexed as

AdolescentCase-Control StudiesCeliac DiseaseChildChild, PreschoolEpigenesis, GeneticFemaleGene Expression ProfilingGenetic MarkersHumansInfantInterferon-gammaIntestinal MucosaIntestine, SmallMachine LearningMaleGenetic MarkersInterferon-gammaRNA, Untranslatedgene expression signaturesimmune cell de-convolutionmachine learningmolecular subgroupspersonalized diagnosticsself-organizing mapsvillous atrophy

Identifiers

PMID33806322
PMCPMC7961974
OpenAlexW3134361734

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.