Volume 68, Issue 5 pp. e77-e80
Short Communication: Gastroenterology: Celiac Disease

Celiac Disease in Brazilian First-degree Relatives

The Odds Are Five Times Greater for HLA DQ2 Homozygous

Letícia H.C. Lopes

Letícia H.C. Lopes

Division of Pediatric Gastroenterology, Pediatric Department, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil

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Janaína G. Muniz

Janaína G. Muniz

Division of Pediatric Gastroenterology, Pediatric Department, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil

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Ricardo P. Oliveira

Ricardo P. Oliveira

Division of Pediatric Gastroenterology, Pediatric Department, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil

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Vera L. Sdepanian

Corresponding Author

Vera L. Sdepanian

Division of Pediatric Gastroenterology, Pediatric Department, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil

Address correspondence and reprint requests to Vera L. Sdepanian, MD, PhD, Division of Pediatric Gastroenterology, Pediatric Department, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Estado de Israel, 577 Apto 112, CEP 04022-001, São Paulo, Brazil (e-mail: [email protected]).Search for more papers by this author
First published: 01 May 2019
Citations: 6

The authors report no conflicts of interest.

ABSTRACT

First-degree relatives (FDRs) of 47 outpatients with celiac disease (CD) answered a questionnaire about symptoms related to CD and were investigated for human leukocyte antigen (HLA)-DQ2, DQB1*02 homozygosis, and DQ8 alleles. Genetically susceptible individuals were tested for antitransglutaminase antibody immunoglobulin A. Seropositive FDR underwent small bowel biopsies.

From 114 FDR, 74.5% (n = 85) were positive for DQ2, DQ8, or both haplotypes. Homozygosity of DQB1*02 was found in 11.4% (n = 13) individuals. Three FDR were previously diagnosed with CD. Among the genetically susceptible individuals, 67.1% had at least 1 symptom related to CD. Seropositivity was 8/82 (9.8%), and 4/8 biopsies were compatible with CD. Therefore, the total number of FDR with CD was 6.1% (7/114), 95% confidence interval (1.71, 10.49). Three out of 7 FDR with CD were HLA DQB1*02 homozygous. The odds of being CD is 5 times, 95% confidence interval (0.99, 26.23), greater for HLA DQ B1*02 homozygous in FDR.

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