Susceptibility to ankylosing spondylitis in twins - The role of genes, HLA, and the environment

被引:495
作者
Brown, MA
Kennedy, LG
MacGregor, AJ
Darke, C
Duncan, E
Shatford, JL
Taylor, A
Calin, A
Wordsworth, P
机构
[1] ROYAL NATL HOSP RHEUMAT DIS,BATH BA1 1RL,AVON,ENGLAND
[2] REG TISSUE TYPING LAB,WELSH BLOOD SERV,PONTYCLUN,WALES
[3] ST THOMAS HOSP,LONDON,ENGLAND
来源
ARTHRITIS AND RHEUMATISM | 1997年 / 40卷 / 10期
关键词
D O I
10.1002/art.1780401015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To determine the relative effects of genetic and environmental factors in susceptibility to ankylosing spondylitis (AS). Methods. Twins with AS were identified from the Royal National Hospital for Rheumatic Diseases database, Clinical and radiographic examinations were performed to establish diagnoses, and disease severity was assessed using a combination of validated scoring systems, HLA typing for HLA-B27, HLA-B60, and HLA-DR1 was performed by polymerase chain reaction with sequence-specific primers, and zygosity was assessed using microsatellite markers, Genetic and environmental variance components were assessed with the program Mx, using data from this and previous studies of twins with AS. Results. Six of 8 monozygotic (MZ) twin pairs were disease concordant, compared with 4 of 15 B27-positive dizygotic (DZ) twin pairs (27%) and 4 of 32 DZ twin pairs overall (12.5%). Nonsignificant increases in similarity with regard to age at disease onset and all of the disease severity scores assessed were noted in disease-concordant MZ twins compared with concordant DZ twins, HLA-B27 and B60 were associated with the disease in probands, and the rate of disease concordance was significantly increased among DZ twin pairs in which the co-twin was positive for both B27 and DR1. Additive genetic effects were estimated to contribute 97% of the population variance, Conclusion. Susceptibility to AS is largely genetically determined, and the environmental trigger for the disease is probably ubiquitous. HLA-B27 accounts for a minority of the overall genetic susceptibility to AS.
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页码:1823 / 1828
页数:6
相关论文
共 29 条
[1]  
ALMAZORMES, 1987, J RHEUMATOL, V14, P302
[2]  
[Anonymous], 1977, Rheumatism in populations
[3]  
BROWN M, 1997, CURRMED LIT, V16, P3
[4]   HLA class I associations of ankylosing spondylitis in the white population in the united Kingdom [J].
Brown, MA ;
Pile, KD ;
Kennedy, LG ;
Calin, A ;
Darke, C ;
Bell, J ;
Wordsworth, BP ;
Cornelis, F .
ANNALS OF THE RHEUMATIC DISEASES, 1996, 55 (04) :268-270
[5]  
BROWN MA, 1995, BR J RHEUMATOL S1, V34, P76
[6]  
BROWN MA, 1995, BR J RHEUMATOL S1, V34, P142
[7]  
CALIN A, 1994, J RHEUMATOL, V21, P2281
[8]   RELATIVE ROLE OF GENETIC AND ENVIRONMENTAL-FACTORS IN DISEASE EXPRESSION - SIB PAIR ANALYSIS IN ANKYLOSING-SPONDYLITIS [J].
CALIN, A ;
ELSWOOD, J .
ARTHRITIS AND RHEUMATISM, 1989, 32 (01) :77-81
[9]  
de Jongh B M, 1990, Scand J Rheumatol Suppl, V87, P127
[10]   HEREDITARY FACTORS IN RHEUMATOID ARTHRITIS AND ANKYLOSING SPONDYLITIS [J].
DEBLECOURT, J ;
POLMAN, A ;
DEBLECOURT, T .
ANNALS OF THE RHEUMATIC DISEASES, 1961, 20 (03) :215-&