## Objective: To determine whether hla-b27 positive patients with ankylosing spondylitis (as) and reactive arthritis (rea) share additional hla factors that confer disease susceptibility. ## Methods: Hla class i antigens were typed serologically, and class ii antigens molecularly, in samples take
The risk of developing ankylosing spondylitis in HLA-B27 positive individuals
✍ Scribed by Sjef M. Der Van Linden; Hans A. Valkenburg; Bartelt M. De Jongh; Arnold Cats
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 903 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The present study was performed on 61 HLA‐B27 positive first‐degree relatives and 40 HLA‐B27 negative relatives of 20 HLA‐B27 positive probands with ankylosing spondylitis (AS). Of 24 HLA‐B27 positive relatives 45 years or older, 21% had AS and 38% sacroiliitis. The HLA‐B27 negative relatives did not have features of either disease. In the population study of 2,957 individuals 45 years or older, we found 5 cases of HLA‐B27 positive sacroiliitis (according to the New York criteria) and 3 of these fulfilled the New York criteria for diagnosis of AS. In 2 of these 3 individuals, the diagnosis was made on clinical grounds. The pheno‐type frequency of HLA‐B27 in this population is 7.8%, or about 230 HLA‐B27 positive individuals in this population sample. Since AS was found in only 3 individuals, 1.3% of the HLA‐B27 positive individuals in the population at large have AS; therefore, our data show that among individuals 45 years or older, 21% of HLA‐B27 positive relatives of HLA‐B27 positive AS patients have AS as compared with 1.3% of the HLA‐B27 positive individuals in the population at large. Thus, the risk for AS is 16 times greater in the HLA‐B27 positive relatives compared with HLA‐B27 positive individuals in the population at large. The discriminatory value of the New York criterion of history of pain or the presence of pain at the dorsolumbar junction or in the lumbar spine was analyzed in the population and family studies and was found to be too nonspecific.
📜 SIMILAR VOLUMES
Objective. To investigate the potential association of tumor necrosis factor a (TNFa) promoter alleles with ankylosing spondylitis. Methods. DNA from 141 HLA-B27 positive Caucasian patients with ankylosing spondylitis and 46 B27-positive and 99 B27-negative healthy Caucasian controls was investigat
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