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A recent genome\u2010wide association study has shown that the genes <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DPB<\/jats:styled-content>1<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DQ<\/jats:styled-content><\/jats:italic> conferred susceptibility to <jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MPA<\/jats:styled-content>, respectively. We investigated the linkage between putative <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content>\u2010related genes (<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DPB<\/jats:styled-content>1<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">ARHGAP<\/jats:styled-content>18<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>226<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">CTLA<\/jats:styled-content>\u20104<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">MOSPD<\/jats:styled-content>2<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">PRTN<\/jats:styled-content>3<\/jats:italic>) and <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content> in a Han Chinese population.<\/jats:p><\/jats:sec><jats:sec><jats:title>Method<\/jats:title><jats:p>A Sequenom MassAarray system (<jats:styled-content style=\"fixed-case\">iPLEX<\/jats:styled-content> assay, Sequenom, San Diego, <jats:styled-content style=\"fixed-case\">CA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> USA<\/jats:styled-content>) was used to genotype single nucleotide polymorphisms (<jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s) in 176 Han Chinese patients with <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content> (100 with <jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content>, 76 with <jats:styled-content style=\"fixed-case\">MPA<\/jats:styled-content>) and 485 ethnically matched healthy controls.<\/jats:p><\/jats:sec><jats:sec><jats:title>Result<\/jats:title><jats:p>The frequency of the rs3117242 variant T allele (<jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DPB<\/jats:styled-content>1<\/jats:italic>) was significantly higher in <jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content> patients than in the controls (68.0% compared with 50.4%, <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\u00a0=\u00a02.09, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>: 1.51\u20132.88, Bonferroni corrected <jats:italic>P<\/jats:italic>\u2010value [<jats:italic>Pc<\/jats:italic>]\u00a0=\u00a06.24E\u20105), but was not significantly different between <jats:styled-content style=\"fixed-case\">MPA<\/jats:styled-content> patients and controls (<jats:italic>Pc<\/jats:italic>\u00a0=\u00a00.14). The same results were obtained via genotype distribution and logistic regression analysis based on three genetic models. The allele and genotype distributions of the other polymorphisms were not significantly associated with <jats:styled-content style=\"fixed-case\">AAV<\/jats:styled-content> patients as a whole or <jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content> or <jats:styled-content style=\"fixed-case\">MPA<\/jats:styled-content> patients considered separately.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The rs3117242 of <jats:italic><jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">DPB<\/jats:styled-content>1<\/jats:italic> could be considered a genetic risk factor for <jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content> in Chinese Han people. These findings provide further insights and clues into the etiology of <jats:styled-content style=\"fixed-case\">GPA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MPA<\/jats:styled-content>.<\/jats:p><\/jats:sec>","DOI":"10.1111\/1756-185x.12561","type":"journal-article","created":{"date-parts":[[2015,5,27]],"date-time":"2015-05-27T17:01:52Z","timestamp":1432746112000},"page":"1009-1015","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":14,"title":["<scp>HLA<\/scp>\u2010<scp>DPB<\/scp>1 variant rs3117242 is associated with anti\u2010neutrophil cytoplasmic antibody\u2010associated vasculitides\u00a0in a Han Chinese population"],"prefix":"10.1111","volume":"20","author":[{"given":"Ziyan","family":"Wu","sequence":"first","affiliation":[{"name":"Department of Rheumatology and Clinical Immunology Peking Union Medical College Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Key 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China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Si","family":"Chen","sequence":"additional","affiliation":[{"name":"Department of Rheumatology and Clinical Immunology Peking Union Medical College Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Key Laboratory of Rheumatology and Clinical Immunology Ministry of Education Beijing China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fei","family":"Sun","sequence":"additional","affiliation":[{"name":"Department of Rheumatology and Clinical Immunology Peking Union Medical College Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Key Laboratory of Rheumatology and Clinical Immunology Ministry of Education Beijing China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ping","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Rheumatology and Clinical Immunology Peking Union Medical College Hospital Chinese 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