HLA–Bw60 increases susceptibility to ankylosing spondylitis in HLA–B27+ patients
Autor: | Muhammad Asim Khan, A. Cats, Glenys Thomson, S van der Linden, A. Russell, Wendy P. Robinson, H.-U. Rentsch |
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Rok vydání: | 1989 |
Předmět: |
musculoskeletal diseases
Canada Genotype Immunology Population Locus (genetics) Human leukocyte antigen Immunogenetics Rheumatology medicine Humans Immunology and Allergy Spondylitis Ankylosing Pharmacology (medical) Allele education Alleles HLA-B27 Antigen Netherlands Ankylosing spondylitis education.field_of_study HLA-B27 Norway business.industry Haplotype medicine.disease United States Phenotype Haplotypes HLA-B Antigens Disease Susceptibility business Switzerland |
Zdroj: | Arthritis & Rheumatism. 32:1135-1141 |
ISSN: | 1529-0131 0004-3591 |
DOI: | 10.1002/anr.1780320912 |
Popis: | We examined the distribution of non-B27 alleles of the HLA-B locus among B27+ patients with ankylosing spondylitis (AS), to detect any additional HLA-B locus allele(s) that may act in conjunction with B27 to increase susceptibility to AS. HLA-Bw60 (or B40 when the Bw60,61 split of B40 was not typed for) was shown to be increased among B27+ AS patients in each of 5 independent data sets. This increase was statistically significant in 4 of the 5 data sets studied, and the overall significance was P less than 0.00001. Susceptibility to AS in B27+ individuals was further increased by a factor of approximately 3 when Bw60 was also present. The distribution of HLA-A alleles on the B27-bearing haplotypes in AS patients was not significantly different from that in normal controls. On the other hand, the distribution of HLA-A alleles on Bw60-bearing haplotypes was significantly different from the distribution of A alleles on Bw60 haplotypes in the general population (P less than 0.0005). Bw60 was not increased in B27- patients with AS. A dominant mode of inheritance generally fits AS; however, our sib pair analysis indicates that the B27,Bw60 disease subgroup follows a more recessive mode of inheritance. |
Databáze: | OpenAIRE |
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