
pmid: 23083754
Ankylosing spondylitis (AS) and spondyloarthritis are strongly genetically determined. The long-standing association with HLA-B27 is well described, although the mechanism by which that association induces AS remains uncertain. Recent developments include the description of HLA-B27 tag single nucleotide polymorphisms in European and Asian populations. An increasing number of non-MHC genetic associations have been reported, which provided amongst other things the first evidence of the involvement of the IL-23 pathway in AS. The association with ERAP1 is now known to be restricted to HLA-B27 positive disease. Preliminary studies on the genetics of axial spondyloarthritis demonstrate a lower HLA-B27 carriage rate compared with AS. Studies with larger samples and including non-European ethnic groups are likely to further advance the understanding of the genetics of AS and spondyloarthritis.
Multifactorial Inheritance, Erap1, Hla-B27, 2745 Rheumatology, Arthritis, Genomics, Aminopeptidases, Polymorphism, Single Nucleotide, White People, Minor Histocompatibility Antigens, Asian People, drug mechanism, Genetics, Humans, Genetic Predisposition to Disease, Spondylitis, Ankylosing, Axial spondyloarthritis, ADRB1 gene, HLA-B27 Antigen, Ankylosing spondylitis
Multifactorial Inheritance, Erap1, Hla-B27, 2745 Rheumatology, Arthritis, Genomics, Aminopeptidases, Polymorphism, Single Nucleotide, White People, Minor Histocompatibility Antigens, Asian People, drug mechanism, Genetics, Humans, Genetic Predisposition to Disease, Spondylitis, Ankylosing, Axial spondyloarthritis, ADRB1 gene, HLA-B27 Antigen, Ankylosing spondylitis
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