Abstract |
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.
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Authors | W P Robinson, S M van der Linden, M A Khan, H U Rentsch, A Cats, A Russell, G Thomson |
Journal | Arthritis and rheumatism
(Arthritis Rheum)
Vol. 32
Issue 9
Pg. 1135-41
(Sep 1989)
ISSN: 0004-3591 [Print] United States |
PMID | 2789045
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- HLA-B Antigens
- HLA-B27 Antigen
- HLA-B60 antigen
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Topics |
- Alleles
- Canada
- Disease Susceptibility
- Genotype
- HLA-B Antigens
(genetics)
- HLA-B27 Antigen
- Haplotypes
- Humans
- Netherlands
- Norway
- Phenotype
- Spondylitis, Ankylosing
(genetics)
- Switzerland
- United States
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