Effects exposure to 0.06 ppm ozone on FEV1 in humans: A secondary analysis of existing data

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Abstract

Background: Ozone is a potent photochemical oxidant that produces transient, reversible decrements in the lung function of acutely exposed individuals. A recent study provided previously unavailable clinical data for 30 healthy young adults exposed to O3 at 0.06 ppm. That study showed significant effects of 0.08 ppm on lung function, confirming the findings of others. However, exposure to 0.06 ppm O3 was not reported to significantly affect lung function. Objectives: We conducted this analysis to reevaluate the existing lung function data of the volunteers previously exposed to 0.06 ppm O3. Methods: We obtained pre- and postexposure data on forced expiratory volume in 1 sec (FEV1) for all subjects who were previously exposed for 6.6 hr to filtered air or to 0.06 ppm or 0.08 ppm O3. We used standard statistical methods appropriate for paired comparisons to reanalyze FEV1 responses after exposure to 0.06 ppm O3 relative to filtered air. Results: Controlling for filtered air responses, 24 of the 30 subjects experienced an O3-induced decrement in FEV1. On average, 0.06 ppm O3 exposure caused a 2.85% reduction in FEV1 (p < 0.002), which was consistent with the predicted FEV1 response from existing models. Although the average response was small, two subjects had > 10% FEV1 decrements. Conclusions: Exposure to 0.06 ppm O3 causes a biologically small but highly statistically significant decrease in mean FEV1 responses of young healthy adults.

Figures

  • Figure 1. Mean FEV1 decrements as function of exposure duration and O3 concentration. Data are for constant, S-W O3 protocols in the Adams (2006) study. Error bars are the SE of responses at 6.6 hr. Adapted from Adams (2006).
  • Table 1. Percent decrement in FEV1 for 6.6 hr of exposure to FA and 0.06 ppm O3 for individuals in the Adams (2006) study.
  • Figure 2. Cross-study comparison of mean O3-induced FEV1 decrements due to 6.6 hr of constant, S-W exposure to varied O3 concentrations. All exposures were conducted in a chamber, except for a face-mask exposure to 0.04 ppm O3 in the Adams (2002) study. All studies used a 6.6-hr exposure protocol in which volunteers alternated between 50 min of exercise (VE ≈ 20 L/min/m2 BSA) and 10 min of rest with an additional 35 min of rest after the third hour. For this exposure protocol, the McDonnell et al. (2007) curve illustrates the predicted FEV1 decrement at 6.6 hr as a function of O3 concentration for a 23-year-old. Error bars (where available) are the SE of responses. The data at 0.08 and 0.12 ppm have been offset for illustrative purposes.
  • Table 2. Descriptive and inferential statistics for O3-induced decrementsa in FEV1 for the full data set (n = 30) and for two data sets with potential outliers removed.

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CITATION STYLE

APA

Brown, J. S., Bateson, T. F., & McDonnell, W. F. (2008). Effects exposure to 0.06 ppm ozone on FEV1 in humans: A secondary analysis of existing data. Environmental Health Perspectives, 116(8), 1023–1026. https://doi.org/10.1289/ehp.11396

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