1998
DOI: 10.1016/s0016-5085(98)81115-3
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HLA DQB1*0401 is associated with the development of atrophic gastritis in H. pylori-infected patients

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Cited by 7 publications
(16 citation statements)
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“…reported that DRB1*1601 was associated with gastric adenocarcinoma. We reported the DQB1*0401 plays an important role in the development of atrophic gastritis in H. pylori infected patients 7 . Although Lee et al 11 .…”
Section: Discussionmentioning
confidence: 79%
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“…reported that DRB1*1601 was associated with gastric adenocarcinoma. We reported the DQB1*0401 plays an important role in the development of atrophic gastritis in H. pylori infected patients 7 . Although Lee et al 11 .…”
Section: Discussionmentioning
confidence: 79%
“…Genomic DNA was obtained from peripheral blood leukocytes and HLA‐DQB1 genotype was defined by the polymerase chain reaction (PCR)‐restriction fragment length polymorphism (RFLP) method 20 . PCR primers for amplification and restriction endonuclease for genotyping of DQB1 alleles were as described previously 7 …”
Section: Methodsmentioning
confidence: 99%
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“…Some HLA class II alleles, such as HLA-DQA1*0102, *0301, and DQB1*0301 and *0401, have been associated with some H. pylori-related diseases. [9][10][11][12][13][14][15][16][17] A lower frequency of the DQA1*0102 allele has been associated Background. The goal of this study was to determine the importance of Helicobacter pylori CagAϩ, VacAϩ, and HLA-DQA1 alleles in a Mexican population with gastric cancer (GC).…”
Section: Introductionmentioning
confidence: 99%
“…Scarce studies have been carried out concerning HLA in H. pylori ‐associated gastroduodenal diseases; among them, the DQA1*01:02 allele was found connected with a reduced risk for atrophic gastritis in a Japanese population, and the DQB1*06:02 allele was related to protection against peptic ulcer disease . In contrast, in another Asian population, the DQB1*04:01 allele was found as risk for atrophic gastritis and duodenal ulcer, DPB1*09:01 and DPA1*02:01 for gastric ulcer, and DRB1*04:05 for duodenal ulcer, whereas to our knowledge only one study has been carried out in Caucasian populations, where DQB1*03:01 was reported linked with GC . Thus, there is a need for extended studies in different populations and in larger patient groups, particularly in regions of Latin America and Asia where burden of GC is more severe.…”
mentioning
confidence: 99%