Genetic Variants of the IL-23R Pathway: Association with Psoriatic Arthritis and Psoriasis Vulgaris, but No Specific Risk Factor for Arthritis

2009 | journal article. A publication with affiliation to the University of Göttingen.

Jump to: Cite & Linked | Documents & Media | Details | Version history

Cite this publication

​Genetic Variants of the IL-23R Pathway: Association with Psoriatic Arthritis and Psoriasis Vulgaris, but No Specific Risk Factor for Arthritis​
Hueffmeier, U.; Lascorz, J.; Boehm, B.; Lohmann, J.; Wendler, J.; Moessner, R. & Reich, K. et al.​ (2009) 
Journal of Investigative Dermatology129(2) pp. 355​-358​.​ DOI: https://doi.org/10.1038/jid.2008.233 

Documents & Media

License

GRO License GRO License

Details

Authors
Hueffmeier, Ulrike; Lascorz, Jesus; Boehm, Beate; Lohmann, Joerg; Wendler, Joerg; Moessner, Rotraut; Reich, Kristian; Traupe, Heiko; Kurrat, Werner; Burkhardt, Harald; Reis, Andre
Abstract
Variants in two genes of the IL-23 receptor (R) pathway have recently been shown to be associated with psoriasis vulgaris (PV). We were interested whether the risk conferred by these variants differs between psoriatic skin and joint disease. Four variants of the IL12B and IL23R genes were analyzed in 1,114 PV patients, 748 patients with psoriatic arthritis (PA) and 937 healthy controls before and after stratification for the major psoriasis risk allele at psoriasis susceptibility locus 1 (PSORS1). For both PA and PV, we detected the strongest association with two IL12B single-nucleotide polymorphisms and the corresponding haplotype as reflected by minimal P-values of 10(-7) and highest odds ratios of 1.50 (1.28-1.75) for rs6887695 in PA patients and 1.50 (1.27-1.76) for rs3212227 in the PV cohort, respectively. For IL23R, only rs11209026 showed an association. The results remained significant after correction for multiple testing. No difference was observed after stratification for the PSORS1 risk allele. While confirming recent reports on variants of the IL-23R pathway as susceptibility factors for PV, our study is the first to extend analysis of both genes to PA. However, our results indicate that these variants are not specific risk factors for arthritis, but relevant for susceptibility to psoriasis in general.
Issue Date
2009
Status
published
Publisher
Nature Publishing Group
Journal
Journal of Investigative Dermatology 
ISSN
0022-202X
Sponsor
University of Erlangen-Nuremberg [IZKF B32/A8]

Reference

Citations


Social Media