Long-term ozone exposure and lung function in middle childhood

被引:0
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作者
Hazlehurst, Marnie F. [1 ,16 ]
Dearborn, Logan C. [1 ]
Sherris, Allison R. [1 ]
Loftus, Christine T. [1 ]
Adgent, Margaret A. [2 ]
Szpiro, Adam A. [3 ]
Ni, Yu [1 ,4 ]
Day, Drew B. [5 ]
Kaufman, Joel D. [6 ,7 ,8 ]
Thakur, Neeta [9 ]
Wright, Rosalind J. [10 ,11 ]
Sathyanarayana, Sheela [12 ,13 ,14 ]
Carroll, Kecia N. [10 ,11 ]
Moore, Paul E. [15 ]
Karr, Catherine J. [12 ,13 ]
机构
[1] Univ Washington, Sch Publ Hlth, Dept Environm & Occupat Hlth Sci, Seattle, WA USA
[2] Vanderbilt Univ Sch Med, Dept Hlth Policy, Nashville, TN USA
[3] Univ Washington, Sch Publ Hlth, Dept Biostat, Seattle, WA USA
[4] San Diego State Univ, Coll Hlth & Human Serv, Sch Publ Hlth, San Diego, CA USA
[5] Seattle Childrens Res Inst, Ctr Child Hlth Behav & Dev Child Hlth, Seattle, WA USA
[6] Univ Washington, Sch Publ Hlth, Dept Pediat, Seattle, WA USA
[7] Univ Washington, Sch Publ Hlth, Dept Environm & Occupat Hlth Sci, Seattle, WA USA
[8] Univ Washington, Sch Med, Dept Med, Seattle, WA USA
[9] Univ Calif San Francisco, Sch Med, Div Pulm & Crit Care Med, San Francisco, CA 94143 USA
[10] Icahn Sch Med Mt Sinai, Dept Environm Med & Publ Hlth, New York, NY USA
[11] Icahn Sch Med Mt Sinai, Dept Pediat, New York, NY USA
[12] Univ Washington, Sch Med, Dept Pediat, Seattle, WA USA
[13] Univ Washington, Sch Publ Hlth, Dept Environm & Occupat Hlth Sci, Seattle, WA USA
[14] Seattle Childrens Res Inst, Seattle, WA USA
[15] Vanderbilt Univ, Med Ctr, Dept Pediat, Div Allergy Immunol & Pulm Med, Nashville, TN USA
[16] 4225 Roosevelt Way NE,Suite 301, Seattle, WA 98405 USA
关键词
Spirometry; Ozone; FEV1; FVC; AMBIENT AIR-POLLUTION; 4-YEAR-OLD CHILDREN; IGE ANTIBODIES; ASTHMA; AGE; BRONCHIOLITIS; SCHOOL; ASSOCIATIONS; DISPARITIES; MORBIDITY;
D O I
10.1016/j.envres.2023.117632
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: Ozone (O3) exposure interrupts normal lung development in animal models. Epidemiologic evidence further suggests impairment with higher long-term O3 exposure across early and middle childhood, although study findings to date are mixed and few have investigated vulnerable subgroups. Methods: Participants from the CANDLE study, a pregnancy cohort in Shelby County, TN, in the ECHOPATHWAYS Consortium, were included if children were born at gestational age >32 weeks, completed a spirometry exam at age 8-9, and had a valid residential history from birth to age 8. We estimated lifetime average ambient O3 exposure based on each child's residential history from birth to age 8, using a validated fineresolution spatiotemporal model. Spirometry was performed at the age 8-9 year study visit to assess Forced Expiratory Volume in the first second (FEV1) and Forced Vital Capacity (FVC) as primary outcomes; z-scores were calculated using sex-and-age-specific reference equations. Linear regression with robust variance estimators was used to examine associations between O3 exposure and continuous lung function z-scores, adjusted for child, sociodemographic, and home environmental factors. Potential susceptible subgroups were explored using a product term in the regression model to assess effect modification by child sex, history of bronchiolitis in infancy, and allergic sensitization. Results: In our sample (n = 648), O3 exposure averaged from birth to age 8 was modest (mean 26.6 [SD 1.1] ppb). No adverse associations between long-term postnatal O3 exposure were observed with either FEV1 (beta = 0.12, 95% CI: -0.04, 0.29) or FVC (beta = 0.03, 95% CI: -0.13, 0.19). No effect modification by child sex, history of bronchiolitis in infancy, or allergic sensitization was detected for associations with 8-year average O3. Conclusions: In this sample with low O3 concentrations, we did not observe adverse associations between O3 exposures averaged from birth to age 8 and lung function in middle childhood.
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页数:9
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