Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci


Autoria(s): Reveille, J. D.; Sims, A. M.; Danoy, P.; Evans, D. M.; Leo, P.; Pointon, J. J.; Jin, R.; Zhou, X.; Bradbury, L. A.; Appleton, L. H.; Davis, J. C.; Diekman, L.; Doan, T.; Dowling, A.; Duan, R.; Duncan, E. L.; Farrar, C.; Hadler, J.; Harvey, D.; Karaderi, T.; Mogg, R.; Pomeroy, E.; Pryce, K.; Taylor, J.; Savage, L.; Deloukas, P.; Kumanduri, V.; Peltonen, L.; Ring, S. M.; Whittaker, P.; Glazov, E.; Thomas, G. P.; Maksymowych, W. P.; Inman, R. D.; Ward, M. M.; Stone, M. A.; Weisman, M. H.; Wordsworth, B. P.; Brown, M. A.
Data(s)

2010

Resumo

To identify susceptibility loci for ankylosing spondylitis, we undertook a genome-wide association study in 2,053 unrelated ankylosing spondylitis cases among people of European descent and 5,140 ethnically matched controls, with replication in an independent cohort of 898 ankylosing spondylitis cases and 1,518 controls. Cases were genotyped with Illumina HumHap370 genotyping chips. In addition to strong association with the major histocompatibility complex (MHC; P 10 800), we found association with SNPs in two gene deserts at 2p15 (rs10865331; combined P = 1.9 × 10 19) and 21q22 (rs2242944; P = 8.3 × 10 20), as well as in the genes ANTXR2 (rs4333130; P = 9.3 × 10 8) and IL1R2 (rs2310173; P = 4.8 × 10 7). We also replicated previously reported associations at IL23R (rs11209026; P = 9.1 × 10 14) and ERAP1 (rs27434; P = 5.3 × 10 12). This study reports four genetic loci associated with ankylosing spondylitis risk and identifies a major role for the interleukin (IL)-23 and IL-1 cytokine pathways in disease susceptibility. © 2010 Nature America, Inc. All rights reserved.

Identificador

http://eprints.qut.edu.au/89383/

Publicador

Nature Publishing Group

Relação

DOI:10.1038/ng.513

Reveille, J. D., Sims, A. M., Danoy, P., Evans, D. M., Leo, P., Pointon, J. J., Jin, R., Zhou, X., Bradbury, L. A., Appleton, L. H., Davis, J. C., Diekman, L., Doan, T., Dowling, A., Duan, R., Duncan, E. L., Farrar, C., Hadler, J., Harvey, D., Karaderi, T., Mogg, R., Pomeroy, E., Pryce, K., Taylor, J., Savage, L., Deloukas, P., Kumanduri, V., Peltonen, L., Ring, S. M., Whittaker, P., Glazov, E., Thomas, G. P., Maksymowych, W. P., Inman, R. D., Ward, M. M., Stone, M. A., Weisman, M. H., Wordsworth, B. P., & Brown, M. A. (2010) Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nature Genetics, 42(2), pp. 123-127.

Direitos

Copyright Nature America Inc

Fonte

Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #interleukin 1 #interleukin 23 #interleukin 23 receptor #adult #ankylosing spondylitis #antxr2 gene #article #chromosome 2p #cohort analysis #controlled study #disease predisposition #ERAP1 gene #female #gene identification #gene locus #gene replication #genetic association #genetic susceptibility #genotype #histocompatibility gene #human #major clinical study #major histocompatibility complex #male #priority journal #single nucleotide polymorphism #Cohort Studies #Genetic Loci #Genetic Predisposition to Disease #Genome-Wide Association Study #Humans #Polymorphism #Single Nucleotide #Reproducibility of Results #Spondylitis #Ankylosing
Tipo

Journal Article