Evidence map›Paper›PMID 17919990›Full record

ArticleClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2007

HLA DQ gene dosage and risk and severity of celiac disease.

Joseph A Murray, S Breanndan Moore, Carol T Van Dyke, Brian D Lahr, Ross A Dierkhising, Alan R Zinsmeister, L Joseph Melton, Cynthia M Kroning, Mounif El-Yousseff, Albert J Czaja

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 16% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 94 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Article
  8. IgA nephropathy.Nature reviews. Disease primers · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Observational
  15. The Liver and Celiac Disease.Clinics in liver disease · 2019
    Review
  16. Article
  17. Article
  18. HLA Typing and Celiac Disease in Moroccans.Medical sciences (Basel, Switzerland) · 2017
    Article
  19. Article
  20. 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

10 authors at 3 institutions in 1 country.

Joseph A MurrayDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA. murray.joseph@mayo.edu
S Breanndan Moore
Carol T Van Dyke
Brian D Lahr
Ross A Dierkhising
Alan R Zinsmeister
L Joseph Melton
Cynthia M Kroning
Mounif El-Yousseff
Albert J Czaja
Mayo Clinic · USCancer Research And Biostatistics · USInstitute for Transfusion Medicine · US

Funding

ZESTRIL VS. VERAPAMIL IN THE TREATMENT OF HYPERTENSIONM01RR000585 · NCRR · MAYO CLINIC ROCHESTER · PI RIZZA, ROBERT A. · 1985 to 2006
$30.4M
ROCHESTER EPIDEMIOLOGY PROJECTR01AR030582 · NIAMS · MAYO CLINIC ROCHESTER · PI ROCCA, WALTER A · 1986 to 2009
$5.1M
EPIDEMIOLOGY OF CELIAC DISEASE--A POPULATION BASED STUDYR01DK057892 · NIDDK · MAYO CLINIC ROCHESTER · PI MURRAY, JOSEPH A · 2000 to 2010
$3.9M
A HLA Mouse Model for Gluten Sensitivity and EnteropathyR01DK071003 · NIDDK · MAYO CLINIC ROCHESTER · PI MURRAY, JOSEPH A · 2006 to 2009
$1.1M
NCRR NIH HHS M01 RR000585NCRR NIH HHS M01 RR00585NIAMS NIH HHS AR 30582NIAMS NIH HHS R01 AR030582NIDDK NIH HHS DK 57982NIDDK NIH HHS R01 DK057892NIDDK NIH HHS R01 DK071003
6 · The paper itself

Abstract

BACKGROUND &

aimsCeliac disease (CD) is a chronic inflammatory disorder of the small intestine that is strongly associated with certain HLA molecules encoded by DQA and DQB genes. The aim of this study was to examine the role of DQA and DQB alleles in determining the risk for and the age of onset and severity of CD in an American population.

methodsHigh-resolution class 2 HLA genotyping was performed in a population-based sample (n = 84) of southeastern Minnesota residents with CD and a comparable control group (n = 102) to determine the contribution of DQA and DQB alleles to disease risk. Logistic regression modeling was used to examine the relative and absolute risks of CD.

resultsNinety-seven percent of CD patients carried both of the HLA alleles, DQA1*05 and DQB1*02. Those who carried a second allele of DQB1*02 were 5 times more likely to have CD than those with just one (95% confidence interval, 1.4-18.1). The carriage of 2 copies of DQB1*02 did not predict either an earlier age of onset or severity of disease.

conclusionsBoth HLA alleles DQA1*05 and DQB1*02 are associated with a greatly increased risk of CD, although the latter has the greater effect. Carrying 2 copies of DQB1*02 was associated with an even greater risk for disease but did not predict an earlier age of onset and diagnosis or disease severity. Assessing the copy number of the DQB1*02 allele might allow for the stratification of disease risk.

Indexed as

AdolescentAdultAgedAged, 80 and overBiopsyCeliac DiseaseChildChild, PreschoolDNAFemaleGene DosageGenetic Predisposition to DiseaseHLA-DQ alpha-ChainsHLA-DQ AntigensHLA-DQ beta-ChainsHumansDNAHLA-DQA1 antigenHLA-DQ alpha-ChainsHLA-DQ AntigensHLA-DQB1 antigenHLA-DQ beta-Chains

Identifiers

PMID17919990
PMCPMC2175211
OpenAlexW1984625129

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.