Evidence map›Paper›PMID 30097691›Full record

ArticleCellular and molecular life sciences : CMLS2018

Celiac disease biomarkers identified by transcriptome analysis of small intestinal biopsies.

Hanna Bragde, Ulf Jansson, Mats Fredrikson, Ewa Grodzinsky, Jan Söderman

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2018. 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
–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

27 citing papers in PubMed.

  1. Trial
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  4. Review
  5. Article
  6. Review
  7. Article
  8. Mild Duodenal Mucosal Injury and Increased Type I Interferon Signaling Are Preludes to Celiac Disease.Laboratory investigation; a journal of technical methods and pathology · 2025
    Article
  9. Article
  10. Article
  11. Molecular analysis of duodenal eosinophilia.The Journal of allergy and clinical immunology · 2023
    Article
  12. Article
  13. Celiac disease: From genetics to epigenetics.World journal of gastroenterology · 2022
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Dissecting the contribution of single nucleotide polymorphisms inJournal of translational autoimmunity · 2021
    Article
  19. Article
  20. Molecular Biomarkers for Celiac Disease: Past, Present and Future.International journal of molecular sciences · 2020
    Review
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

5 authors.

Hanna BragdeLaboratory Medicine, Ryhov County Hospital, Building E3 Level 4, 55185, Jönköping, Sweden. hanna.gustafsson.bragde@rjl.se.ORCID http://orcid.org/0000-0001-9104-3863
Ulf JanssonDepartment of Pediatrics, Ryhov County Hospital, Jönköping, Sweden.
Mats FredriksonDepartment of Clinical and Experimental Medicine and Forum Östergötland, Faculty of Medicine and Health Sciences, Linköping University, Linköping, Sweden.
Ewa GrodzinskyDivision of Forensic Genetics & Forensic Toxicology, National Board of Forensic Medicine, Linköping, Sweden.
Jan SödermanLaboratory Medicine, Ryhov County Hospital, Building E3 Level 4, 55185, Jönköping, Sweden.ORCID http://orcid.org/0000-0001-7505-7210

Funding

Forskningsrådet i Sydöstra Sverige FORSS-230451Futurum - the Academy for Health and Care FUTURUM-708171
6 · The paper itself

Abstract

Establishing a celiac disease (CD) diagnosis can be difficult, such as when CD-specific antibody levels are just above cutoff or when small intestinal biopsies show low-grade injuries. To investigate the biological pathways involved in CD and select potential biomarkers to aid in CD diagnosis, RNA sequencing of duodenal biopsies from subjects with either confirmed Active CD (n = 20) or without any signs of CD (n = 20) was performed. Gene enrichment and pathway analysis highlighted contexts, such as immune response, microbial infection, phagocytosis, intestinal barrier function, metabolism, and transportation. Twenty-nine potential CD biomarkers were selected based on differential expression and biological context. The biomarkers were validated by real-time polymerase chain reaction of eight RNA sequencing study subjects, and further investigated using an independent study group (n = 43) consisting of subjects not affected by CD, with a clear diagnosis of CD on either a gluten-containing or a gluten-free diet, or with low-grade intestinal injury. Selected biomarkers were able to classify subjects with clear CD/non-CD status, and a subset of the biomarkers (CXCL10, GBP5, IFI27, IFNG, and UBD) showed differential expression in biopsies from subjects with no or low-grade intestinal injury that received a CD diagnosis based on biopsies taken at a later time point. A large number of pathways are involved in CD pathogenesis, and gene expression is affected in CD mucosa already in low-grade intestinal injuries. RNA sequencing of low-grade intestinal injuries might discover pathways and biomarkers involved in early stages of CD pathogenesis.

Indexed as

AdolescentBiomarkersBiopsyCeliac DiseaseChildChild, PreschoolFemaleGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansInfantIntestinal MucosaIntestine, SmallMaleBiomarkersGene expression profilingGene ontology enrichment analysisMolecular biomarkersRNA-seqRNA sequencing

Identifiers

PMID30097691
PMCPMC6208765

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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.