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PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus

OBJECTIVES: Psoriatic arthritis (PsA) is a chronic inflammatory arthritis associated with psoriasis; it has a higher estimated genetic component than psoriasis alone, however most genetic susceptibility loci identified for PsA to date are also shared with psoriasis. Here we attempt to validate novel...

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Autores principales: Bowes, John, Loehr, Sabine, Budu-Aggrey, Ashley, Uebe, Steffen, Bruce, Ian N, Feletar, Marie, Marzo-Ortega, Helena, Helliwell, Philip, Ryan, Anthony W, Kane, David, Korendowych, Eleanor, Alenius, Gerd-Marie, Giardina, Emiliano, Packham, Jonathan, McManus, Ross, FitzGerald, Oliver, Brown, Matthew A, Behrens, Frank, Burkhardt, Harald, McHugh, Neil, Huffmeier, Ulrike, Ho, Pauline, Reis, Andre, Barton, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602265/
https://www.ncbi.nlm.nih.gov/pubmed/25923216
http://dx.doi.org/10.1136/annrheumdis-2014-207187
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author Bowes, John
Loehr, Sabine
Budu-Aggrey, Ashley
Uebe, Steffen
Bruce, Ian N
Feletar, Marie
Marzo-Ortega, Helena
Helliwell, Philip
Ryan, Anthony W
Kane, David
Korendowych, Eleanor
Alenius, Gerd-Marie
Giardina, Emiliano
Packham, Jonathan
McManus, Ross
FitzGerald, Oliver
Brown, Matthew A
Behrens, Frank
Burkhardt, Harald
McHugh, Neil
Huffmeier, Ulrike
Ho, Pauline
Reis, Andre
Barton, Anne
author_facet Bowes, John
Loehr, Sabine
Budu-Aggrey, Ashley
Uebe, Steffen
Bruce, Ian N
Feletar, Marie
Marzo-Ortega, Helena
Helliwell, Philip
Ryan, Anthony W
Kane, David
Korendowych, Eleanor
Alenius, Gerd-Marie
Giardina, Emiliano
Packham, Jonathan
McManus, Ross
FitzGerald, Oliver
Brown, Matthew A
Behrens, Frank
Burkhardt, Harald
McHugh, Neil
Huffmeier, Ulrike
Ho, Pauline
Reis, Andre
Barton, Anne
author_sort Bowes, John
collection PubMed
description OBJECTIVES: Psoriatic arthritis (PsA) is a chronic inflammatory arthritis associated with psoriasis; it has a higher estimated genetic component than psoriasis alone, however most genetic susceptibility loci identified for PsA to date are also shared with psoriasis. Here we attempt to validate novel single nucleotide polymorphisms selected from our recent PsA Immunochip study and determine specificity to PsA. METHODS: A total of 15 single nucleotide polymorphisms were selected (P(Immunochip) <1×10(−4)) for validation genotyping in 1177 cases and 2155 controls using TaqMan. Meta-analysis of Immunochip and validation data sets consisted of 3139 PsA cases and 11 078 controls. Novel PsA susceptibility loci were compared with data from two large psoriasis studies (WTCCC2 and Immunochip) to determine PsA specificity. RESULTS: We found genome-wide significant association to rs2476601, mapping to PTPN22 (p=1.49×10(−9), OR=1.32), but no evidence for association in the psoriasis cohort (p=0.34) and the effect estimates were significantly different between PsA and psoriasis (p=3.2×10(−4)). Additionally, we found genome-wide significant association to the previously reported psoriasis risk loci; NOS2 (rs4795067, p=5.27×10(−9)). CONCLUSIONS: For the first time, we report genome-wide significant association of PTPN22 (rs2476601) to PsA susceptibility, but no evidence for association to psoriasis.
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spelling pubmed-46022652015-10-21 PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus Bowes, John Loehr, Sabine Budu-Aggrey, Ashley Uebe, Steffen Bruce, Ian N Feletar, Marie Marzo-Ortega, Helena Helliwell, Philip Ryan, Anthony W Kane, David Korendowych, Eleanor Alenius, Gerd-Marie Giardina, Emiliano Packham, Jonathan McManus, Ross FitzGerald, Oliver Brown, Matthew A Behrens, Frank Burkhardt, Harald McHugh, Neil Huffmeier, Ulrike Ho, Pauline Reis, Andre Barton, Anne Ann Rheum Dis Clinical and Epidemiological Research OBJECTIVES: Psoriatic arthritis (PsA) is a chronic inflammatory arthritis associated with psoriasis; it has a higher estimated genetic component than psoriasis alone, however most genetic susceptibility loci identified for PsA to date are also shared with psoriasis. Here we attempt to validate novel single nucleotide polymorphisms selected from our recent PsA Immunochip study and determine specificity to PsA. METHODS: A total of 15 single nucleotide polymorphisms were selected (P(Immunochip) <1×10(−4)) for validation genotyping in 1177 cases and 2155 controls using TaqMan. Meta-analysis of Immunochip and validation data sets consisted of 3139 PsA cases and 11 078 controls. Novel PsA susceptibility loci were compared with data from two large psoriasis studies (WTCCC2 and Immunochip) to determine PsA specificity. RESULTS: We found genome-wide significant association to rs2476601, mapping to PTPN22 (p=1.49×10(−9), OR=1.32), but no evidence for association in the psoriasis cohort (p=0.34) and the effect estimates were significantly different between PsA and psoriasis (p=3.2×10(−4)). Additionally, we found genome-wide significant association to the previously reported psoriasis risk loci; NOS2 (rs4795067, p=5.27×10(−9)). CONCLUSIONS: For the first time, we report genome-wide significant association of PTPN22 (rs2476601) to PsA susceptibility, but no evidence for association to psoriasis. BMJ Publishing Group 2015-10 2015-04-28 /pmc/articles/PMC4602265/ /pubmed/25923216 http://dx.doi.org/10.1136/annrheumdis-2014-207187 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Clinical and Epidemiological Research
Bowes, John
Loehr, Sabine
Budu-Aggrey, Ashley
Uebe, Steffen
Bruce, Ian N
Feletar, Marie
Marzo-Ortega, Helena
Helliwell, Philip
Ryan, Anthony W
Kane, David
Korendowych, Eleanor
Alenius, Gerd-Marie
Giardina, Emiliano
Packham, Jonathan
McManus, Ross
FitzGerald, Oliver
Brown, Matthew A
Behrens, Frank
Burkhardt, Harald
McHugh, Neil
Huffmeier, Ulrike
Ho, Pauline
Reis, Andre
Barton, Anne
PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus
title PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus
title_full PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus
title_fullStr PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus
title_full_unstemmed PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus
title_short PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus
title_sort ptpn22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further psa-specific risk locus
topic Clinical and Epidemiological Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602265/
https://www.ncbi.nlm.nih.gov/pubmed/25923216
http://dx.doi.org/10.1136/annrheumdis-2014-207187
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