Evidence map›Paper›PMID 25172978›Full record

ArticleBosnian journal of basic medical sciences2014

HLA genotyping in pediatric celiac disease patients.

Biljana Stanković, Nedeljko Radlović, Zoran Leković, Dragana Ristić, Vladimir Radlović, Gordana Nikčević, Nikola Kotur, Ksenija Vučićević, Tatjana Kostić, Sonja Pavlović and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Bosnian journal of basic medical sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Human Leukocyte Antigen-DQ Genotyping in Pediatric Celiac Disease.Pediatric gastroenterology, hepatology & nutrition · 2023
    Article
  8. Review
  9. Review
  10. Article
  11. Early Infant Feeding Practices May Influence the Onset of Symptomatic Celiac Disease.Pediatric gastroenterology, hepatology & nutrition · 2016
    Article
  12. Article
  13. Celiac crisis in children in Serbia.Italian journal of pediatrics · 2016
    Article
  14. Genetic susceptibility for celiac disease is highly prevalent in the Saudi population.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association
    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

11 authors at 3 institutions in 2 countries.

Biljana StankovićInstitute of Molecular Genetics and Genetic Engineering, University of Belgrade. bi.stankovic@gmail.com.
Nedeljko Radlović
Zoran Leković
Dragana Ristić
Vladimir Radlović
Gordana Nikčević
Nikola Kotur
Ksenija Vučićević
Tatjana Kostić
Sonja Pavlović
Branka Zukic
University of Belgrade · RSInstitute of Molecular Genetics · RUUniversity of Kragujevac · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Celiac disease (CD) is a chronic inflammatory disease in the small intestine triggered by gluten uptake that occurs in genetically susceptible individuals. HLA-DQ2 protein encoded by HLA-DQA1*05 and DQB1*02 alleles is found in 90-95% of CD patients. All of the remaining patients carry HLA-DQ8 protein encoded by HLA-DQA1*03 and DQB1*03:02 alleles. Specific HLA-DQ genotypes define different risk for CD incidence. Presence of susceptible HLA-DQ genotypes does not predict certain disease development, but their absence makes CD very unlikely, close to 100%. Here we presented for the first time the distribution of HLA-DQ genotypes in the group of pediatric celiac patients from the University Children's Hospital, Belgrade, Serbia and estimated risk for CD development that these genotypes confer. Seventy three celiac disease patients and 62 healthy individuals underwent genotyping for DQA1, DQB alleles and DRB1 allele. 94.5% of patients carried alleles that encode DQ2 protein variant and 2.7% carried alleles that encode DQ8 protein variant. Two patients carried single DQB1*02 allele. No patients were negative for all the alleles predisposing to CD. The highest HLA-DQ genotype risk for CD development was found in group of patients homozygous for DQ2.5 haplotype, followed by the group of heterozygous carriers of DQ2.5 haplotype in combination with DQB1*02 allele within the other haplotype. The lowest risk was observed in carriers of a single copy of DQB1*02 or DQA1*05 allele or other non-predisposing alleles. HLA genotyping, more informative than serological testing commonly used, proved to be a useful diagnostic tool for excluding CD development.

Indexed as

AdolescentAdultAllelesCase-Control StudiesCeliac DiseaseChildChild, PreschoolFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHaplotypesHLA-DQ alpha-ChainsHLA-DQ AntigensHomozygoteHumansHLA-DQ2 antigenHLA-DQ8 antigenHLA-DQA1 antigenHLA-DQ alpha-ChainsHLA-DQ Antigens

Identifiers

PMID25172978
PMCPMC4333989
OpenAlexW2120212735

What OpenQuestion holds

Textmetadata
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.