TY - JOUR
T1 - Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis
AU - Bowes, John
AU - Budu-Aggrey, Ashley
AU - Huffmeier, Ulrike
AU - Uebe, Steffen
AU - Steel, Kathryn
AU - Hebert, Harry L.
AU - Wallace, Chris
AU - Massey, Jonathan
AU - Bruce, Ian N.
AU - Bluett, James
AU - Feletar, Marie
AU - Morgan, Ann W.
AU - Marzo-Ortega, Helena
AU - Donohoe, Gary
AU - Morris, Derek W.
AU - Helliwell, Philip
AU - Ryan, Anthony W.
AU - Kane, David
AU - Warren, Richard B.
AU - Korendowych, Eleanor
AU - Alenius, Gerd-Marie
AU - Giardina, Emiliano
AU - Packham, Jonathan
AU - McManus, Ross
AU - Fitzgerald, Oliver
AU - McHugh, Neil
AU - Brown, Matthew A.
AU - Ho, Pauline
AU - Behrens, Frank
AU - Burkhardt, Harald
AU - Reis, Andre
AU - Barton, Anne
N1 - Publisher Copyright:
© 2015 Macmillan Publishers Limited. All rights reserved.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Psoriatic arthritis (PsA) is a chronic inflammatory arthritis associated with psoriasis and, despite the larger estimated heritability for PsA, the majority of genetic susceptibility loci identified to date are shared with psoriasis. Here, we present results from a case-control association study on 1,962 PsA patients and 8,923 controls using the Immunochip genotyping array. We identify eight loci passing genome-wide significance, secondary independent effects at three loci and a distinct PsA-specific variant at the IL23R locus. We report two novel loci and evidence of a novel PsA-specific association at chromosome 5q31. Imputation of classical HLA alleles, amino acids and SNPs across the MHC region highlights three independent associations to class I genes. Finally, we find an enrichment of associated variants to markers of open chromatin in CD8+ memory primary T cells. This study identifies key insights into the genetics of PsA that could begin to explain fundamental differences between psoriasis and PsA.
AB - Psoriatic arthritis (PsA) is a chronic inflammatory arthritis associated with psoriasis and, despite the larger estimated heritability for PsA, the majority of genetic susceptibility loci identified to date are shared with psoriasis. Here, we present results from a case-control association study on 1,962 PsA patients and 8,923 controls using the Immunochip genotyping array. We identify eight loci passing genome-wide significance, secondary independent effects at three loci and a distinct PsA-specific variant at the IL23R locus. We report two novel loci and evidence of a novel PsA-specific association at chromosome 5q31. Imputation of classical HLA alleles, amino acids and SNPs across the MHC region highlights three independent associations to class I genes. Finally, we find an enrichment of associated variants to markers of open chromatin in CD8+ memory primary T cells. This study identifies key insights into the genetics of PsA that could begin to explain fundamental differences between psoriasis and PsA.
UR - http://hdl.handle.net/10379/10495
UR - https://www.scopus.com/pages/publications/84923253404
U2 - 10.13025/27579
DO - 10.13025/27579
M3 - Article
SN - 2041-1723
VL - 6
JO - Nature Communications
JF - Nature Communications
M1 - 6046
ER -