Evidence map›Paper›PMID 29358886›Full record

Observational studyWorld journal of gastroenterology2018

HLA-DQ: Celiac disease

Marta Maia Bosca-Watts, Miguel Minguez, Dolores Planelles, Samuel Navarro, Alejandro Rodriguez, Jesus Santiago, Joan Tosca, Francisco Mora

Open access · hybridAbstract readComparative StudyObservational Study
In one paragraph

Observational study in World journal of gastroenterology, 2018. 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
2.9field-weighted citation impact, top 9% 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, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Haplotype Analysis Reveals Pleiotropic Disease Associations in the HLA Region.medRxiv : the preprint server for health sciences · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. 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

8 authors at 4 institutions in 1 country.

Marta Maia Bosca-WattsIBD Unit, Digestive Disease Department of the University Clinic Hospital of Valencia, University of Valencia, Valencia 46017, Spain. inflamatoriahcuv@gmail.com.
Miguel MinguezIBD Unit, Digestive Disease Department of the University Clinic Hospital of Valencia, University of Valencia, Valencia 46017, Spain.
Dolores PlanellesHistocompatibility Department of the Transfusion Center of the Valencian Community, Valencia 46014, Spain.
Samuel NavarroPathology Department of the University Clinic Hospital of Valencia, University of Valencia, Valencia 46017, Spain.
Alejandro RodriguezDigestive Disease Department of the Hospital Virgen del Castillo of Yecla, Yecla 30510, Spain.
Jesus SantiagoDigestive Disease Department of the Hospital de Manises, Valencia 46940, Spain.
Joan ToscaIBD Unit, Digestive Disease Department of the University Clinic Hospital of Valencia, University of Valencia, Valencia 46017, Spain.
Francisco MoraDigestive Disease Department of the University Clinic Hospital of Valencia, University of Valencia, Valencia 46017, Spain.
Universitat de València · ESGeneralitat Valenciana · ESHospital Clínico Universitario de Valencia · ESHospital de Manises · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo determine the genetic predisposition to celiac disease (CeD) in inflammatory bowel disease (IBD) patients by quantifying the frequency of CeD-related human leucocyte antigen (HLA) (HLA-CeD: HLA-DQ2 and -DQ8) in IBD patients globally, by type of IBD and gender, and by calculating the protective/risk contribution of these haplotypes in the development of the IBD disease.

methodsWe conducted a prospective study with IBD patients from our Unit. Clinical information was gathered and blood was tested for HLA-CeD. The control group was made up of unrelated Valencian organ donors.

results1034 subjects were analyzed: 457 IBD [207 ulcerative coliti (UC) and 250 Crohn's disease (CD)] patients and 577 healthy controls. 39% of the controls and 34% of the patients had HLA-CeD (

conclusionHLA-CeD is not more frequent in IBD patients, with an even lower frequency of HLA-DQ2 and -DQ8 in UC and CD respectively. HLA-DQ2.5 confers protection from the development of UC, especially in women, and HLA-DQ8 does so for the appearance of CD. HLA-DQ2.2 is present in 34% of the CD patients and may constitute a genetic risk factor for CD development.

Indexed as

Case-Control StudiesCeliac DiseaseColitis, UlcerativeCrohn DiseaseFemaleGene FrequencyGenetic Predisposition to DiseaseHaplotypesHLA-DQ AntigensHumansMalePhenotypeProspective StudiesProtective FactorsRisk FactorsSex FactorsHLA-DQ2 antigenHLA-DQ8 antigenHLA-DQ AntigensCeliac diseaseCrohn’s diseaseGenetic predispositionHuman leucocyte antigenInflammatory bowel diseaseUlcerative colitis

Identifiers

PMID29358886
PMCPMC5757130
OpenAlexW2781706032

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.