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Familial risk of seropositive rheumatoid arthritis and interaction with smoking: a population-based cohort study

Authors
Kim, Hyun JungSwan, HeatherKazmi, Sayada ZartashaHong, GahwiKim, Young ShinChoi, SeeunKang, TaeukCha, JaewooEom, JungminHann, Hoo JaeChoi, In AhAhn, Hyeong Sik
Issue Date
Jan-2023
Publisher
Oxford University Press
Keywords
RA; familial risk; additive interaction; smoking
Citation
Rheumatology
Indexed
SCIE
SCOPUS
Journal Title
Rheumatology
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/62450
DOI
10.1093/rheumatology/kead048
ISSN
1462-0324
1462-0332
Abstract
Objectives We evaluated the familial risk of seropositive rheumatoid arthritis (RA) and examined interactions between family history and smoking. Methods Using the National Health Insurance and Health Screening Program databases, which include information on familial relationships and lifestyle factors, we identified 5 524 403 individuals with first-degree relatives (FDRs) from 2002–2018. We calculated familial risk using hazard ratios (HRs) with 95% CIs which compare the risk of individuals with and without affected FDRs. Interactions between smoking and family history were assessed on an additive scale using the relative excess risk due to interaction (RERI). Results Individuals with affected FDR had 4.52-fold (95% CI 3.98, 5.12) increased risk of disease compared with those with unaffected FDR. Familial risk adjusted for lifestyle factors decreased slightly (HR 4.49), suggesting that a genetic contribution is the predominant driver in the familial aggregation of RA. Smoking was associated with an increased risk of disease that was more pronounced among heavy (HR 1.92 95% CI 1.70, 2.18) compared with moderate (HR 1.15 95% CI 1.04, 1.28) smoking. In the interaction analysis, the risk associated with the combined effect of smoking and family history was higher than the sum of their individual effects, though statistically non-significant (RERI 1.30 95% CI ‒0.92, 3.51). Heavy smokers with a positive family history showed a prominent interaction (RERI 4.13 95% CI ‒0.88, 9.13) which exceeded moderate smokers (RERI 0.61 95% CI ‒1.90, 3.13), suggesting a dose-response interaction pattern. Conclusion Our findings indicate the possibility of an interaction between RA-associated genes and smoking.
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1. Basic Science > Department of Preventive Medicine > 1. Journal Articles
3. Graduate School > Graduate School > 1. Journal Articles

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