Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis.
Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis.
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DOI:
10.1038/gene.2012.17
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发表时间:
2012-09
影响因子:
5
通讯作者:
Seldin, M. F.
中科院分区:
文献类型:
--
作者:
Invernizzi, P.;Ransom, M.;Raychaudhuri, S.;Kosoy, R.;Lleo, A.;Shigeta, R.;Franke, A.;Bossa, F.;Amos, C. I.;Gregersen, P. K.;Siminovitch, K. A.;Cusi, D.;de Bakker, P. I. W.;Podda, M.;Gershwin, M. E.;Seldin, M. F.
Susceptibility to primary biliary cirrhosis (PBC) is strongly associated with HLA region polymorphisms. To determine if associations can be explained by classical HLA determinants we studied Italian 676 cases and 1440 controls with genotyped with dense single nucleotide polymorphisms (SNPs) for which classical HLA alleles and amino acids were imputed. Although previous genome-wide association studies and our results show stronger SNP associations near DQB1, we demonstrate that the HLA signals can be attributed to classical DRB1 and DPB1 genes. Strong support for the predominant role of DRB1 is provided by our conditional analyses. We also demonstrate an independent association of DPB1. Specific HLA-DRB1 genes (*08, *11 and *14) account for most of the DRB1 association signal. Consistent with previous studies, DRB1*08 (p = 1.59 × 10−11) was the strongest predisposing allele where as DRB1*11 (p = 1.42 × 10−10) was protective. Additionally DRB1*14 and the DPB1 association (DPB1*03:01) (p = 9.18 × 10−7) were predisposing risk alleles. No signal was observed in the HLA class 1 or class 3 regions. These findings better define the association of PBC with HLA and specifically support the role of classical HLA-DRB1 and DPB1 genes and alleles in susceptibility to PBC.
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DOI:
10.1111/j.1463-1326.2008.00997.x
发表时间:
2009-02
期刊:
Diabetes, obesity & metabolism
影响因子:
--
作者:
Brown WM;Pierce J;Hilner JE;Perdue LH;Lohman K;Li L;Venkatesh RB;Hunt S;Mychaleckyj JC;Deloukas P;Type 1 Diabetes Genetics Consortium
通讯作者:
Type 1 Diabetes Genetics Consortium
影响因子:
5
作者:
Bergamaschi, L.;Leone, M. A.;D'Alfonso, S.
通讯作者:
D'Alfonso, S.
影响因子:
3.9
作者:
Kosoy, Roman;Nassir, Rami;Tian, Chao;White, Phoebe A.;Butler, Lesley M.;Silva, Gabriel;Kittles, Rick;Alarcon-Riquelme, Marta E.;Gregersen, Peter K.;Belmont, John W.;De La Vega, Francisco M.;Seldin, Michael F.
通讯作者:
Seldin, Michael F.
影响因子:
3.7
作者:
Field J;Browning SR;Johnson LJ;Danoy P;Varney MD;Tait BD;Gandhi KS;Charlesworth JC;Heard RN;Australia and New Zealand Multiple Sclerosis Genetics Consortium;Stewart GJ;Kilpatrick TJ;Foote SJ;Bahlo M;Butzkueven H;Wiley J;Booth DR;Taylor BV;Brown MA;Rubio JP;Stankovich J
通讯作者:
Stankovich J
影响因子:
13.5
作者:
Donaldson, Peter T.;Baragiotta, Anna;Bassendine, Margaret F.
通讯作者:
Bassendine, Margaret F.