{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T07:23:40Z","timestamp":1789025020823,"version":"build-2803163510"},"reference-count":34,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2017,2,28]],"date-time":"2017-02-28T00:00:00Z","timestamp":1488240000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100004191","name":"Novo Nordisk","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100004191","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["HLA"],"published-print":{"date-parts":[[2017,5]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Type 1 diabetes (<jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content>) and celiac disease (<jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content>) are 2 distinct diseases, but there is an increased risk of developing <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> for <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> patients. Both diseases are associated with <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010class <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content> alleles, such as <jats:styled-content style=\"fixed-case\">\n<jats:italic>DQB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*02:01<\/jats:italic> and <jats:styled-content style=\"fixed-case\">\n<jats:italic>DQB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*03:02<\/jats:italic>; however, their risk contribution vary between the diseases.<\/jats:p><\/jats:sec><jats:sec><jats:title>Materials and Methods<\/jats:title><jats:p>We genotyped <jats:italic>\n<jats:styled-content style=\"fixed-case\">HLA\u2010DRB1<\/jats:styled-content>\n<\/jats:italic> and \u2013<jats:italic>\n<jats:styled-content style=\"fixed-case\">DQB1<\/jats:styled-content>\n<\/jats:italic> in 215 patients with coexisting <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> identified from a <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> cohort, and compared them to patients with <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> (N\u2009=\u2009487) and <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> (N\u2009=\u2009327), as well as healthy controls (N\u2009=\u2009368).<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The patients with coexisting <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> had an intermediate carrier frequency (72.8%) of the <jats:styled-content style=\"fixed-case\">\n<jats:italic>DRB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*03:01\u2010<\/jats:italic>\n<jats:styled-content style=\"fixed-case\">\n<jats:italic>DQB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*02:01\u2010<\/jats:italic>\n<jats:styled-content style=\"fixed-case\">\n<jats:italic>DQA1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*05:01<\/jats:italic> haplotype compared to <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> (64.1%) and <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> (88.7%) patients. The <jats:styled-content style=\"fixed-case\">\n<jats:italic>DRB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*03:01\u2010<\/jats:italic>\n<jats:styled-content style=\"fixed-case\">\n<jats:italic>DQB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*02:01\u2010<\/jats:italic>\n<jats:styled-content style=\"fixed-case\">\n<jats:italic>DQA1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*05:01\/<\/jats:italic>\n<jats:styled-content style=\"fixed-case\">\n<jats:italic>DRB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*04\u2010<\/jats:italic>\n<jats:styled-content style=\"fixed-case\">\n<jats:italic>DQB1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*03:02\u2010<\/jats:italic>\n<jats:styled-content style=\"fixed-case\">\n<jats:italic>DQA1<\/jats:italic>\n<\/jats:styled-content>\n<jats:italic>*03<\/jats:italic> haplotype combination, encoding <jats:styled-content style=\"fixed-case\">DQ2<\/jats:styled-content>.5 and <jats:styled-content style=\"fixed-case\">DQ8<\/jats:styled-content> molecules, was equally frequent among patients with both <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> (52.6%) and <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> patients (46.8%) but significantly lower in <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> patients (9.5%).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Overall, the patients with coexisting <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> had an <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content> profile more similar to <jats:styled-content style=\"fixed-case\">T1D<\/jats:styled-content> patients than <jats:styled-content style=\"fixed-case\">CeD<\/jats:styled-content> patients.<\/jats:p><\/jats:sec>","DOI":"10.1111\/tan.12986","type":"journal-article","created":{"date-parts":[[2017,3,1]],"date-time":"2017-03-01T04:07:24Z","timestamp":1488341244000},"page":"278-284","source":"Crossref","is-referenced-by-count":21,"title":["<scp>HLA<\/scp> class <scp>II<\/scp> alleles in Norwegian patients with coexisting type 1 diabetes and celiac disease"],"prefix":"10.1111","volume":"89","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3917-9269","authenticated-orcid":false,"given":"M. K.","family":"Viken","sequence":"first","affiliation":[{"name":"Department of Immunology Oslo University Hospital and University of Oslo  Oslo Norway"},{"name":"Department of Medical Genetics University of Oslo and Oslo University Hospital  Oslo Norway"},{"name":"Oslo Diabetes Research Centre  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. T.","family":"Fl\u00e5m","sequence":"additional","affiliation":[{"name":"Department of Medical Genetics University of Oslo and Oslo University Hospital  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T.","family":"Skrivarhaug","sequence":"additional","affiliation":[{"name":"Oslo Diabetes Research Centre  Oslo Norway"},{"name":"Department of Paediatrics, Division of Paediatric and Adolescent Medicine Oslo University Hospital  Oslo Norway"},{"name":"The Norwegian Childhood Diabetes Registry, Division of Paediatric and Adolescent Medicine Oslo University Hospital  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. S.","family":"Amundsen","sequence":"additional","affiliation":[{"name":"Department of Immunology Oslo University Hospital and University of Oslo  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L. M.","family":"Sollid","sequence":"additional","affiliation":[{"name":"Department of Immunology Oslo University Hospital and University of Oslo  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. K.","family":"Drivvoll","sequence":"additional","affiliation":[{"name":"The Norwegian Childhood Diabetes Registry, Division of Paediatric and Adolescent Medicine Oslo University Hospital  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G.","family":"Joner","sequence":"additional","affiliation":[{"name":"Department of Paediatrics, Division of Paediatric and Adolescent Medicine Oslo University Hospital  Oslo Norway"},{"name":"Institute of Clinical Medicine, Faculty of Medicine University of Oslo  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K.","family":"Dahl\u2010J\u00f8rgensen","sequence":"additional","affiliation":[{"name":"Oslo Diabetes Research Centre  Oslo Norway"},{"name":"Department of Paediatrics, Division of Paediatric and Adolescent Medicine Oslo University Hospital  Oslo Norway"},{"name":"Institute of Clinical Medicine, Faculty of Medicine University of Oslo  Oslo Norway"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B. 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