4.8 Article

Prenatal exposure to arsenic and lung function in children from the New Hampshire Birth Cohort Study

Journal

ENVIRONMENT INTERNATIONAL
Volume 155, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.envint.2021.106673

Keywords

Children; Lung capacity; Arsenic speciation; Gestational exposure; Spirometry

Funding

  1. [P01ES022832]
  2. [RD83544201]
  3. [R25CA134286]
  4. [P42ES007373]
  5. [UH3OD023275]
  6. [CIDEGENT/2020/050]

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The study found that prenatal arsenic exposure may have an adverse effect on childhood lung function, particularly on forced vital capacity and forced expiratory volume in the first second of exhalation. This negative impact may be more pronounced, especially among girls, when the mother has a lower secondary methylation index.
Prenatal arsenic exposure is associated with an increased risk of lung cancer along with multiple non-carcinogenic outcomes, including respiratory diseases in arsenic-contaminated areas. Limited epidemiologic data exist on whether in utero arsenic exposure influences lung development and subsequent respiratory health. We investigated the association between gestational arsenic exposure and childhood lung function in the New Hampshire Birth Cohort Study. Urinary arsenic speciation including inorganic arsenic (iAs), monomethylarsonic acid (MMA), dimethylarsinic acid (DMA) and arsenobetaine was measured in maternal urine samples collected during pregnancy and spirometry was performed in offspring at a median age of 7.4 years. Forced vital capacity (FVC), forced expiratory volume in the first second of exhalation (FEV1), and forced expiratory flow between 25% and 75% of FVC (FEF25-75) standardized z-scores were assessed in linear models as dependent variables with the log(2)-transformed summation of urinary arsenic species (Sigma As = iAs + MMA + DMA) corrected for specific gravity as an independent variable and with adjustment for maternal smoking status, children's age, sex and height. Among the 358 children in the study, a doubling of Sigma As was associated with a 0.08 (beta) decrease in FVC z-scores (95% confidence interval (CI) from 0.14 to 0.01) and 0.10 (beta) (95% CI from 0.18 to 0.02) decrease in FEV1 z-scores. The inverse association appeared stronger among those mothers with lower secondary methylation index (urinary DMA/MMA), especially among girls. No association was observed for FEF25-75 z-scores. Our results suggest that gestation arsenic exposure at levels relevant to the general US population during the vulnerable period of lung formation may adversely affect lung function in childhood.

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