HLA class I and II alleles in susceptibility to ankylosing spondylitis.
HLA class I and II alleles in susceptibility to ankylosing spondylitis.
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DOI:
10.1136/annrheumdis-2018-213779
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发表时间:
2019-01
影响因子:
27.4
通讯作者:
Brown MA
中科院分区:
文献类型:
--
作者:
Reveille JD;Zhou X;Lee M;Weisman MH;Yi L;Gensler LS;Zou H;Ward MM;Ishimori ML;Learch TJ;He D;Rahbar MH;Wang J;Brown MA
To examine associations of HLA class I and class II alleles with ankylosing spondylitis (AS) in three cohorts of patients of European, Asian and African ancestry. HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1 alleles were genotyped in 1948 unrelated white and 67 African-American AS patients from the Prospective Study of Outcomes in Ankylosing Spondylitis (PSOAS) cohort, the North American Spondylitis Consortium (NASC) and Australo-Anglo-American Spondyloarthritis Consortium (TASC), 990 white and 245 African American Controls and HLA-B alleles in 442 Han Chinese AS patients and 346 controls from Shanghai and Gansu, China. In addition to the case:control analyses, HLA-B*27 negative AS patients were analyzed separately, and logistic regression and “relative predispositional effects” (RPE) analyses were carried out to control for the major effect of HLA-B*27on disease susceptibility. Although numerous associations were seen between HLA alleles and AS in whites, among HLA-B*27 negative AS patients, positive associations were seen with HLA-A*29, B*38, B*49, B*52, DRB1*11 and DPB1*03:01 and negative associations with HLA-B*07, -B*57, -DRB1*15:01, -DQB1*02:01 and -DQB1*06:02. Additional associations with HLA-B*14 and B*40 (B60) were observed via RPE analysis, which excludes the HLA-B*27 alleles. The increased frequency of HLA-B*40:01 and decreased frequency of HLA-B*07 was also seen in Han Chinese and African-Americans with AS. HLA-B*08 was decreased in whites with acute anterior uveitis. These data, analyzing the largest number of AS patients examined to date in three ethnic groups, confirm that other HLA class I and II alleles other than HLA-B*27 to be operative in AS predisposition.
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影响因子:
2.9
作者:
Londono, John;Maria Santos, Ana;Medina, Juan F.
通讯作者:
Medina, Juan F.
影响因子:
30.8
作者:
Ellinghaus D;Jostins L;Spain SL;Cortes A;Bethune J;Han B;Park YR;Raychaudhuri S;Pouget JG;Hübenthal M;Folseraas T;Wang Y;Esko T;Metspalu A;Westra HJ;Franke L;Pers TH;Weersma RK;Collij V;D'Amato M;Halfvarson J;Jensen AB;Lieb W;Degenhardt F;Forstner AJ;Hofmann A;International IBD Genetics Consortium (IIBDGC);International Genetics of Ankylosing Spondylitis Consortium (IGAS);International PSC Study Group (IPSCSG);Genetic Analysis of Psoriasis Consortium (GAPC);Psoriasis Association Genetics Extension (PAGE);Schreiber S;Mrowietz U;Juran BD;Lazaridis KN;Brunak S;Dale AM;Trembath RC;Weidinger S;Weichenthal M;Ellinghaus E;Elder JT;Barker JN;Andreassen OA;McGovern DP;Karlsen TH;Barrett JC;Parkes M;Brown MA;Franke A
通讯作者:
Franke A
影响因子:
29.4
作者:
Orchard, TR;Thiyagaraja, S;Jewell, DP
通讯作者:
Jewell, DP
影响因子:
27.4
作者:
van Gaalen, Floris A.;Verduijn, Willem;Toes, Rene E. M.
通讯作者:
Toes, Rene E. M.
影响因子:
30.8
作者:
Goyette, Philippe;Boucher, Gabrielle;Mallon, Dermot;Ellinghaust, Eva;Jostins, Luke;Huang, Hailiang;Ripke, Stephan;Gusareva, Elena S.;Annese, Vito;Hauser, Stephen L.;Oksenberg, Jorge R.;Thomsent, Ingo;Leslie, Stephen;Daly, Mark J.;Van Steen, Kristel;Duerr, Richard H.;Barrett, Jeffrey C.;McGovern, Dermot P. B.;Schumm, L. Philip;Traherne, James A.;Carrington, Mary N.;Kosmoliaptsis, Vasilis;Karsen, Tom H.;Franke, Andre;Rioux, John D.
通讯作者:
Rioux, John D.