4.5 Article

Passive Smoking Throughout the Life Course and the Risk of Incident Rheumatoid Arthritis in Adulthood Among Women

期刊

ARTHRITIS & RHEUMATOLOGY
卷 73, 期 12, 页码 2219-2228

出版社

WILEY
DOI: 10.1002/art.41939

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资金

  1. Rheumatology Research Foundation R Bridge Award
  2. NIH [L30-AR-066953, K24-AR-052403, R01-AR-049880, R01-AR-057327, R01-AR-119246, R01-HL-034594, P30-AR-070253, P30-AR-072577, P30-AR-069625, UM1-CA-186107, U01-HG-008685, 1OT2-OD-026553, R03-AR-075886, U01-CA-176726, R01-CA-67262, U01-HL-145386]
  3. Rheumatology Research Foundation K Bridge Award
  4. Brigham and Women's Hospital Department of Medicine Fellowship Award
  5. National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH [K23-AR-076453, K23-AR-069688]

向作者/读者索取更多资源

Childhood parental smoking was found to be associated with adult-onset incident seropositive RA, even after controlling for adulthood personal smoking. Maternal smoking during pregnancy was also linked to RA, but this association weakened after considering subsequent smoking exposures.
Objective To investigate passive smoking throughout the life course and the risk of rheumatoid arthritis (RA), while accounting for personal smoking. Methods We analyzed the Nurses' Health Study II prospective cohort, using information collected via biennial questionnaires. We assessed the influence of 1) maternal smoking during pregnancy (in utero exposure), 2) childhood parental smoking, and 3) years lived with smokers since age 18. Incident RA and serostatus were determined by medical record review. Using the marginal structural model framework, we estimated the controlled direct effect of each passive smoking exposure on adult incident RA risk by serologic phenotype, controlling for early-life factors and time-updated adulthood factors including personal smoking. Results Among 90,923 women, we identified 532 incident RA cases (66% seropositive) during a median of 27.7 years of follow-up. Maternal smoking during pregnancy was associated with RA after adjustment for confounders, with a hazard ratio (HR) of 1.25 (95% confidence interval [95% CI] 1.03-1.52), but not after accounting for subsequent smoking exposures. Childhood parental smoking was associated with seropositive RA after adjustment for confounders (HR 1.41 [95% CI 1.08-1.83]). In the controlled direct effect analyses, childhood parental smoking was associated with seropositive RA (HR 1.75 [95% CI 1.03-2.98]) after controlling for adulthood personal smoking, and the association was accentuated among ever smokers (HR 2.18 [95% CI 1.23-3.88]). There was no significant association of adulthood passive smoking with RA (HR 1.30 for >= 20 years of living with a smoker versus none [95% CI 0.97-1.74]). Conclusion We found a potential direct influence of childhood parental smoking on adult-onset incident seropositive RA even after controlling for adulthood personal smoking.

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