ArticleWorld journal of gastroenterology2013
Human leukocyte antigen DQ2/8 prevalence in non-celiac patients with gastrointestinal diseases.
Article in World journal of gastroenterology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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Who cites it
14 citing papers in PubMed, 25 citations in OpenAlex.
- Dietary Intervention for Systemic Lupus Erythematosus patients based on HLA-DQ2 and DQ8 genotyping (DISH): a protocol for a randomised controlled study.Lupus science & medicine · 2025Article
- HLA-DQ and alcohol in the pathogenesis of irritable bowel syndrome in college students: a case-control study.Scientific reports · 2023Article
- Gluten Degradation by the Gut Microbiota of Ulcerative Colitis Patients.Microorganisms · 2022Article
- The frequency of HLA-DQ2/DQ8 haplotypes and celiac disease among the first-degree relatives of patients with celiac disease.Gastroenterology and hepatology from bed to bench · 2021Article
- Evaluation of the Utility of Amino Acid Citrulline as a Surrogate Metabolomic Biomarker for the Diagnosis of Celiac Disease.Nutrition and metabolic insights · 2021Article
- Non-celiac gluten sensitivity as a rare cause of growth retardation in children: a case series study.Gastroenterology and hepatology from bed to bench · 2021Article
- A simple treatment for a potentially life-threatening cause of malabsorption.Internal and emergency medicine · 2019Article
- Angiotensin II receptor blockers and gastrointestinal adverse events of resembling sprue-like enteropathy: a systematic review.Gastroenterology report · 2019Review
- Olmesartan is not associated with the risk of enteropathy: a Korean nationwide observational cohort study.The Korean journal of internal medicine · 2019Observational
- Treatment of irritable bowel syndrome.Australian prescriber · 2018Review
- The distribution of HLA DQ2 and DQ8 haplotypes and their association with health indicators in a general Danish population.United European gastroenterology journal · 2018Article
- HLA-DQ: Celiac diseaseWorld journal of gastroenterology · 2018Observational
- Article
- Immunogenetic biomarkers in inflammatory bowel diseases: role of the IBD3 region.World journal of gastroenterology · 2014Review
Corrections and comments
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Authors and funding
8 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
aimTo investigate the prevalence of human leukocyte antigen (HLA) DQ2/8 alleles in Southern Italians with liver and gastrointestinal (GI) diseases outside of celiac disease.
methodsHLA DQ2/8 status was assessed in 443 patients from three ambulatory gastroenterology clinics in Southern Italy (University of Federico II, Naples, Loreto Crispi Hospital, Ruggi D'Aragona Hospital, Salerno). Patients were grouped based on disease status [pre-post transplant liver disease, esophageal/gastric organic and functional diseases, irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD)] and DQ2/8 alleles, which correspond to a celiac disease genetic risk gradient. Subject allele frequencies were compared to healthy Italian controls.
resultsOne hundred and ninety-six out of four hundred and forty-three (44.2%) subjects, median age 56 years and 42.6% female, were DQ2/8 positive. When stratifying by disease we found that 86/188 (45.7%) patients with liver disease were HLA DQ2/8 positive, 39/73 (53.4%) with functional upper GI diseases and 19/41 (46.3%) with organic upper GI diseases were positive. Furthermore, 38/105 (36.2%) patients with IBS and 14/36 (38.9%) with IBD were HLA DQ2/8 positive (P = 0.21). Compared to healthy controls those with functional upper GI diseases disorders had a 1.8 times higher odds of DQ2/8 positivity. Those with liver disease had 1.3 times the odds, albeit not statistically significant, of DQ2/8 positivity. Both those with IBS and IBD had a lower odds of DQ2/8 positivity compared to healthy controls.
conclusionThe proportion of individuals HLA DQ2/8 positive is higher in those with liver/upper functional GI disease and lower in IBS/IBD as compared to general population estimates.
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