Association between Kawasaki Disease and Prenatal Exposure to Ambient and Industrial Air Pollution: A Population-Based Cohort Study

被引:14
作者
Buteau, Stephane [1 ,2 ]
Belkaibech, Sabrina [1 ,3 ]
Bilodeau-Bertrand, Marianne [1 ]
Hatzopoulou, Marianne [4 ]
Smargiassi, Audrey [1 ,2 ,5 ]
Auger, Nathalie [1 ,6 ,7 ,8 ]
机构
[1] Inst Natl Sante Publ Quebec, 190 Cremazie Blvd E, Montreal, PQ H2P 1E2, Canada
[2] Univ Montreal, Sch Publ Hlth, Dept Environm & Occupat Hlth, Montreal, PQ, Canada
[3] Univ Lille, Dept Engn & Hlth Management, Lille, France
[4] Univ Toronto, Dept Civil Engn, Toronto, ON, Canada
[5] Univ Montreal, Publ Hlth Res Inst, Montreal, PQ, Canada
[6] Univ Montreal, Univ Montreal Hosp, Res Ctr, Montreal, PQ, Canada
[7] Univ Montreal, Sch Publ Hlth, Dept Social & Prevent Med, Montreal, PQ, Canada
[8] McGill Univ, Dept Epidemiol Biostat & Occupat Hlth, Montreal, PQ, Canada
关键词
SPATIAL VARIABILITY; OXIDATIVE STRESS; MODELS; PM2.5; EPIDEMIOLOGY; PREGNANCY; ETIOLOGY; MONTREAL; QUALITY; RISK;
D O I
10.1289/EHP6920
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BACKGROUND: Environmental factors may contribute to the development of Kawasaki disease in children, but prenatal environmental exposures are understudied. OBJECTIVE: We used a population-based cohort to investigate whether prenatal exposure to outdoor air pollution is associated with the incidence of Kawasaki disease in childhood. METHODS: We performed a longitudinal cohort study of all children born in Quebec, Canada, between 2006 and 2012. Children were, followed for Kawasaki disease from birth until 31 March 2018. We assigned prenatal air pollutant exposure according to the residential postal code at birth. The main exposure was annual average concentration of ambient line particulate matter [PM <= 2.5 mu m in aerodynamic diameter (PM2.5) and nitrogen dioxide (NO2) from satellite-based estimates and land-use regression models. As secondary exposures, we considered industrial PM2.5, NO2, and sulfur dioxide (SO2) emissions estimated from dispersion models. We estimated hazard ratios (HRs) using Cox proportional hazards models, adjusted for maternal age, parity, sex, multiple birth, maternal smoking during pregnancy, socioeconomic status, birth year, and rural residence. We considered single and multipollutant models. We performed several sensitivity analyses, including assessing modifying effects of maternal. comorbidities (e.g., diabetes, preeclampsia). RESULTS: The cohort comprised 505,336 children, including 539 with Kawasaki disease. HRs for each interquartile range increase in ambient air pollution were 1.16 (95% CI: 0.96, 1.39) for PM2.5 and 1.12 (95% CI: 0.96, 1.31) for NO2. For industrial air pollution, HRs were 1.07 (95% CI: 1.01, 1.13) for SO2, 1.09 (95% CI: 0.99, 1.20) for NO2, and 1.01 (95% CI: 0.97, 1.05) for PM2.5. In multipollutant models, associations for ambient PM2.5 and NO2 (i.e., from all sources) were robust to adjustment for industrial pollution, and vice versa. DISCUSSION: In this population-based cohort study, both prenatal exposure to ambient and industrial air pollution were associated with the incidence of Kawasaki disease in childhood. Further studies are needed to consolidate the observed associations.
引用
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页码:1 / 8
页数:8
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