Is disease severity in ankylosing spondylitis genetically determined?
Open Access
- 6 June 2001
- journal article
- research article
- Published by Wiley in Arthritis & Rheumatism
- Vol. 44 (6) , 1396-1400
- https://doi.org/10.1002/1529-0131(200106)44:6<1396::aid-art233>3.0.co;2-a
Abstract
Objective To assess the role of genes and the environment in determining the severity of ankylosing spondylitis. Methods One hundred seventy‐three families with >1 case of ankylosing spondylitis were recruited (120 affected sibling pairs, 26 affected parent–child pairs, 20 families with both first‐ and second‐degree relatives affected, and 7 families with only second‐degree relatives affected), comprising a total of 384 affected individuals. Disease severity was assessed by the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and functional impairment was determined using the Bath Ankylosing Spondylitis Functional Index (BASFI). Disease duration and age at onset were also studied. Variance‐components modeling was used to determine the genetic and environmental components contributing to familiality of the traits examined, and complex segregation analysis was performed to assess different disease models. Results Both the disease activity and functional capacity as assessed by the BASDAI and the BASFI, respectively, were found to be highly familial (BASDAI familiality 0.51 [P = 10−4], BASFI familiality 0.68 [P = 3 × 10−7]). No significant shared environmental component was demonstrated to be associated with either the BASDAI or the BASFI. Including age at disease onset and duration of disease as covariates made no difference in the heritability assessments. A strong correlation was noted between the BASDAI and the BASFI (genetic correlation 0.9), suggesting the presence of shared determinants of these 2 measures. However, there was significant residual heritability for each measure independent of the other (BASFI residual heritability 0.48, BASDAI 0.36), perhaps indicating that not all genes influencing disease activity influence chronicity. No significant heritability of age at disease onset was found (heritability 0.18; P = 0.2). Segregation studies suggested the presence of a single major gene influencing the BASDAI and the BASFI. Conclusion This study demonstrates a major genetic contribution to disease severity in ankylosing spondylitis. As with susceptibility to ankylosing spondylitis, shared environmental factors play little role in determining the disease severity.Keywords
This publication has 18 references indexed in Scilit:
- The bath ankylosing spondylitis radiology index (BASRI): A new, validated approach to disease assessmentArthritis & Rheumatism, 1998
- A genome‐wide screen for susceptibility loci in ankylosing spondylitisArthritis & Rheumatism, 1998
- Susceptibility to ankylosing spondylitis in twins the role of genes, HLA, and the environmentArthritis & Rheumatism, 1997
- Predisposing factors to spondyloarthropathiesCurrent Opinion in Rheumatology, 1997
- THE BATH ANKYLOSING SPONDYLITIS PATIENT GLOBAL SCORE (BAS-G)Rheumatology, 1996
- Investigating the genetic basis for ankylosing spondylitis. Linkage studies with the major histocompatibility complex regionArthritis & Rheumatism, 1994
- Relative role of genetic and environmental factors in disease expression: sib pair analysis in ankylosing spondylitisArthritis & Rheumatism, 1989
- Evaluation of Diagnostic Criteria for Ankylosing SpondylitisArthritis & Rheumatism, 1984
- The histocompatibility antigen (HL-A 27) and diseaseSeminars in Arthritis and Rheumatism, 1975
- High Association of an HL-A Antigen, W27, with Ankylosing SpondylitisNew England Journal of Medicine, 1973