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Association of Helicobacter pylori ‐related Distal Gastric Cancer with the HLA Class II Gene DQB1 * 0602 and cagA + Strains in a Southern European Population
Author(s) -
Quintero Enrique,
Pizarro Ma. Angeles,
Rodrigo Luis,
Piqué Josep M.,
Lanas Angel,
Ponce Julio,
Miño Gonzalo,
Gisbert Javier,
Jurado Aurora,
Herrero Ma. José,
Jiménez Alejandro,
Torrado Julio,
Ponte Ana,
DíazdeRojas Francisco,
Salido Eduardo
Publication year - 2005
Publication title -
helicobacter
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.206
H-Index - 79
eISSN - 1523-5378
pISSN - 1083-4389
DOI - 10.1111/j.1523-5378.2005.00287.x
Subject(s) - caga , helicobacter pylori , genotype , gastroenterology , medicine , genotyping , human leukocyte antigen , cancer , allele , population , immunology , biology , antigen , gene , genetics , environmental health , virulence
Background. Distinct human leukocyte antigen (HLA)‐DQ genes have been associated with an increased or reduced risk for gastric cancer, but its association with Helicobacter pylori status is controversial. In the present study we evaluated the influence of host HLA DQA1 and DQB1 loci, H. pylori genotype, and socio‐economic factors on predicting H. pylori ‐associated distal gastric cancer in a southern European population. Material and methods. In a prospective case–control (1 : 2) study, 42 patients with H. pylori ‐associated distal gastric cancer were matched by age (±5 years) and gender to 84 patients with H. pylori ‐associated benign gastroduodenal disease (controls). The level of education received, smoking status, alcohol consumption, origin and familial history of gastric cancer were registered at inclusion. HLA DQA1 and DQB1 typing and H. pylori genotyping were determined from endoscopic gastric mucosal biopsies. Results. Compared with control patients, a positive association with cagA + strains ( p < .002) and a negative association with vacA‐s2 strains ( p < .02) was found in patients with distal gastric cancer. At the DQB1 locus, the * 0602 allele was more frequent in distal gastric cancer than in controls (26.2% vs. 4.8%; p < .005). After correction for multiple comparisons (exact multiple regression analysis) the cagA + status and the DQB1 * 0602 allele were associated with an increased distal gastric cancer risk (OR 3.7; 95% CI = 1.33–12.26 and OR 4.82; 95% CI = 1.24–19.83, respectively) whereas the vacA‐s2 status was associated with a decreased risk (OR 0.33; 95% CI = 0.10–0.94). Conclusion. Our findings suggest that in the H. pylori ‐infected southern European population, the cagA genotype and the HLA‐DQB1 * 0602 gene confer an increased risk for distal gastric cancer.