Chang-Fu Kuo
Familial risk of Sjögren's syndrome and co-aggregation of autoimmune diseases in affected families: a nationwide population study
Kuo, Chang-Fu; Grainge, Matthew J.; Valdes, Ana M.; See, Lai-Chu; Luo, Shue-Fen; Yu, Kuang-Hui; Zhang, Weiya; Doherty, Michael
Authors
Dr MATTHEW GRAINGE MATTHEW.GRAINGE@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
Professor ANA VALDES Ana.Valdes@nottingham.ac.uk
PROFESSOR OF MOLECULAR & GENETIC EPIDEMIOLOGY
Lai-Chu See
Shue-Fen Luo
Kuang-Hui Yu
Professor WEIYA ZHANG WEIYA.ZHANG@NOTTINGHAM.AC.UK
PROFESSOR OF EPIDEMIOLOGY
Michael Doherty
Abstract
Objective: To investigate familial aggregation of Sjögren's syndrome (SS) and the relative risks (RRs) of other autoimmune disease in relatives of patients with SS.
Methods: We identified 23,658,577 beneficiaries enrolled in the Taiwan National Health Insurance system in 2010, of whom 12,754 had SS. We identified 21,009,551 parent–child relationships and 17,168,340 pairs of full siblings. The familial risks of SS and other autoimmune diseases, tetrachoric correlation, and familial transmission were estimated.
Results: We identified 105 patients with SS who had an affected first-degree relative. The RR of SS was 18.99 (95% confidence interval [95% CI] 9.76–36.93) in siblings of patients with SS, 11.31 (95% CI 8.34–15.33) in offspring, and 12.46 (95% CI 9.34–16.62) in parents. Tetrachoric correlation coefficients were 0.53 (95% CI 0.41–0.65) for cotwins of affected individuals and 0.21 (95% CI 0.16–0.26) for full siblings. The familial transmission (heritability plus shared environmental contribution) was 0.54 (95% CI 0.44–0.77). In first-degree relatives of patients with SS, the RRs were 2.95 (95% CI 2.33–3.73) for rheumatoid arthritis, 6.25 (95% CI 5.15–7.58) for systemic lupus erythematosus, 2.39 (95% CI 0.77–7.41) for systemic sclerosis, 0.71 (95% CI 0.10–5.07) for idiopathic inflammatory myopathy, 1.97 (95% CI 1.29–3.02) for type 1 diabetes mellitus, 3.38 (95% CI 1.26–9.05) for multiple sclerosis, 1.67 (95% CI 0.83–3.33) for myasthenia gravis, 1.25 (95% CI 1.04–1.50) for psoriasis, 1.21 (95% CI 0.39–3.76) for inflammatory bowel disease, and 2.29 (95% CI 1.19–4.40) for vasculitis.
Conclusion: The risk of SS and other autoimmune diseases is increased in relatives of patients with SS, and more than one-half of phenotypic variance in SS can be explained by familial factors.
Citation
Kuo, C.-F., Grainge, M. J., Valdes, A. M., See, L.-C., Luo, S.-F., Yu, K.-H., Zhang, W., & Doherty, M. (2015). Familial risk of Sjögren's syndrome and co-aggregation of autoimmune diseases in affected families: a nationwide population study. Arthritis and Rheumatology, 67(7), 1904-1912. https://doi.org/10.1002/art.39127
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 19, 2015 |
Online Publication Date | Jun 26, 2015 |
Publication Date | 2015-07 |
Deposit Date | Aug 18, 2016 |
Publicly Available Date | Aug 18, 2016 |
Journal | Arthritis & Rheumatology |
Print ISSN | 2326-5191 |
Electronic ISSN | 2326-5205 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 67 |
Issue | 7 |
Pages | 1904-1912 |
DOI | https://doi.org/10.1002/art.39127 |
Public URL | https://nottingham-repository.worktribe.com/output/753678 |
Publisher URL | http://onlinelibrary.wiley.com/doi/10.1002/art.39127/abstract |
Contract Date | Aug 18, 2016 |
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0
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