A polymorphism within the interleukin 1 receptor antagonist (IL-1Ra) gene is associated with ankylosing spondylitis

被引:80
作者
McGarry, F
Neilly, J
Anderson, N
Sturrock, R
Field, M
机构
[1] Univ Glasgow, Glasgow Royal Infirm, Dept Med, Ctr Rheumat Dis, Glasgow G31 2ER, Lanark, Scotland
[2] Univ Glasgow, Western Infirm, Dept Med & Therapeut, Glasgow G11 6NT, Lanark, Scotland
关键词
ankylosing spondylitis; interleukin; 1; genetics; restriction fragment length polymorphism; variable number tandem repeat;
D O I
10.1093/rheumatology/40.12.1359
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Genetic factors that predispose individuals to ankylosing spondylitis (AS) are not fully understood, but are unlikely to be restricted to HLA-B27. Proinflammatory cytokines are implicated in the development of sacroiliitis. We have examined the allele frequencies of three polymorphic sites in the interleukin (IL)-1 genes in AS patients to investigate whether genetic regulation of IL-1 production could be implicated in AS pathogenesis. Methods. DNA from 188 AS patients, 115 healthy controls and 81 HLA-B27-positive healthy controls, all from the West of Scotland, were examined with the polymerase chain reaction in a case-controlled study. Polymorphic sites in genes of the IL-1 family were examined, including the 86-base pair variable number tandem repeat within intron 2 of the IL-1Ra gene, and the restriction fragment length polymorphisms at positions -889 in the IL-1alpha gene and -511 in the IL-1beta gene. Results. No significant differences were seen at the polymorphic alleles in the IL-1alpha and IL-1beta genes, but there was a significant increase in the carriage of allele 2 in the IL-1Ra in the AS patients compared with local controls (16 vs 8%, odds ratio 2.3, 95% confidence interval 1.2-4.4, P=0.01). Conclusion. This report of an association with a polymorphic site within the IL-1 locus and AS suggests that genes other than B27 may well be involved in the pathogenesis of AS.
引用
收藏
页码:1359 / 1364
页数:6
相关论文
共 37 条
[1]  
BENNETT PH, EXC MED FDN AMSTERDA, V148, P456
[2]  
Blakemore AIF, 1996, HUM GENET, V97, P369, DOI 10.1007/BF02185776
[3]  
Braun J, 1999, ARTHRITIS RHEUM, V42, P2039, DOI 10.1002/1529-0131(199910)42:10<2039::AID-ANR3>3.0.CO
[4]  
2-6
[5]   USE OF IMMUNOHISTOLOGIC AND IN-SITU HYBRIDIZATION TECHNIQUES IN THE EXAMINATION OF SACROILIAC JOINT BIOPSY SPECIMENS FROM PATIENTS WITH ANKYLOSING-SPONDYLITIS [J].
BRAUN, J ;
BOLLOW, M ;
NEURE, L ;
SEIPELT, E ;
SEYREKBASAN, F ;
HERBST, H ;
EGGENS, U ;
DISTLER, A ;
SIEPER, J .
ARTHRITIS AND RHEUMATISM, 1995, 38 (04) :499-505
[6]  
BREWERTON DA, 1973, LANCET, V1, P904
[7]  
Brown MA, 1998, ARTHRITIS RHEUM, V41, P588, DOI 10.1002/1529-0131(199804)41:4<588::AID-ART5>3.0.CO
[8]  
2-0
[9]   Susceptibility to ankylosing spondylitis in twins - The role of genes, HLA, and the environment [J].
Brown, MA ;
Kennedy, LG ;
MacGregor, AJ ;
Darke, C ;
Duncan, E ;
Shatford, JL ;
Taylor, A ;
Calin, A ;
Wordsworth, P .
ARTHRITIS AND RHEUMATISM, 1997, 40 (10) :1823-1828
[10]  
Carter MJ, 1999, GASTROENTEROLOGY, V116, pA677