Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
By J. Reveille, A. Sims, P. Danoy, David Evans, P. Leo, Jennifer J. Pointon, Rui Jin, Xiaodong Zhou, L. Bradbury, L. Appleton and 29 more. Nature Genetics, 2010
690 citations recorded by the source corpus.
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.
Subfields: Immunology, Rheumatology
View Paper: https://www.semanticscholar.org/paper/75fc805526588bed45d5ada75095ed9ac46e1316
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Citations in the corpus
- Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility (2011, background): “In addition to its strong association with HLA-B27, ankylosing spondylitis has been convincingly associated with loci containing the genes IL23R , ERAP1 and KIF21B and with the 2p15 and 21q22 intergenic region”