{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,26]],"date-time":"2025-11-26T16:26:14Z","timestamp":1764174374885},"reference-count":40,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2017,3,5]],"date-time":"2017-03-05T00:00:00Z","timestamp":1488672000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["81172857","81373188"],"award-info":[{"award-number":["81172857","81373188"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100007225","name":"Ministry of Science and Technology","doi-asserted-by":"publisher","award":["2011AA02A113"],"award-info":[{"award-number":["2011AA02A113"]}],"id":[{"id":"10.13039\/100007225","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Int J of Rheum Dis"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Aim<\/jats:title><jats:p>Takayasu arteritis (<jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content>) is a rare autoimmune disease with ethnic differences. Genome\u2010wide association studies (<jats:styled-content style=\"fixed-case\">GWAS<\/jats:styled-content>) showed novel genetic variants in the human leukocyte antigen (<jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>) region were associated with <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content>. The present study aimed to investigate the linkage between these single nucleotide polymorphisms (<jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>) and <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> in a Chinese Han population.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Four hundred and twelve patients from multiple centers and 597 healthy controls were genotyped using the Sequenom MassArray <jats:styled-content style=\"fixed-case\">iPLEX<\/jats:styled-content> platform. The association between these <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s and various clinical symptom of <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> was also investigated.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Our study showed a higher risk allele frequency of rs12524487 in <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> patients compared to healthy controls (26.6% <jats:italic>vs<\/jats:italic>. 21.7%, odds ratio [<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>] 1.31, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content> 1.06\u20131.61). The other <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content> rs9366782 in <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010B\/<jats:styled-content style=\"fixed-case\">MICA<\/jats:styled-content> (major histocompatibility complex class I polypeptide\u2010related sequence A) showed association with <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> ischemic brain disease (<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>: 1.78, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>: 1.16\u20132.73, <jats:italic>P<\/jats:italic><jats:sub>c<\/jats:sub> = 0.03). However, rs3763288 and rs114202986 in <jats:styled-content style=\"fixed-case\">MICA<\/jats:styled-content> were negatively related to <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> either as a whole or in any clinical features. Meanwhile, <jats:styled-content style=\"fixed-case\">ATGT<\/jats:styled-content>(rs9366782, rs12524487, rs3763288 and rs114202986) were the risk haplotypes (<jats:italic>P<\/jats:italic><jats:sub>c<\/jats:sub> = 2.48 \u00d7 10<jats:sup>\u221210<\/jats:sup>).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Our findings indicated that rs12524487 in <jats:styled-content style=\"fixed-case\">HLA<\/jats:styled-content>\u2010B\/<jats:styled-content style=\"fixed-case\">MICA<\/jats:styled-content> was a genetic risk factor for <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> in a Chinese Han population and rs9366782 in this region was associated with ischemic brain disease in <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> but not <jats:styled-content style=\"fixed-case\">TA<\/jats:styled-content> susceptibility.<\/jats:p><\/jats:sec>","DOI":"10.1111\/1756-185x.13012","type":"journal-article","created":{"date-parts":[[2017,3,6]],"date-time":"2017-03-06T02:16:39Z","timestamp":1488766599000},"page":"271-277","update-policy":"http:\/\/dx.doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["Association between genetic variants in the human leukocyte antigen\u2010B\/<scp>MICA<\/scp> and Takayasu arteritis in Chinese Han population"],"prefix":"10.1111","volume":"21","author":[{"given":"Xiaoting","family":"Wen","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 Laboratory of Rheumatology and Clinical Immunology Ministry of Education Beijing 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"},{"name":"Department of Clinical Laboratory Beijing Anzhen Hospital Capital Medical University Beijing China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jing","family":"Li","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":"Yuan","family":"Li","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":"Liubing","family":"Li","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":"Ziyan","family":"Wu","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 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