Nonlinearity in human health response to ozone: Experimental laboratory considerations

被引:24
作者
Hazucha, Milan J.
Lefohn, Allen S.
机构
[1] Univ N Carolina, Ctr Environm Med Asthma & Lung Biol, Chapel Hill, NC 27599 USA
[2] ASL & Associates, Helena, MT 59601 USA
关键词
confounders and other influences; diurnal variability; human health response; nonlinear dose-response; threshold; sigmoidal model; FEV(1); ozone standard; 0.12 PPM OZONE; OBSTRUCTIVE PULMONARY-DISEASE; EFFECTIVE DOSE CONCEPT; INDUCED FEV1 CHANGES; RESPIRATORY RESPONSES; EXERCISING CHILDREN; TRIANGULAR PROFILES; PROTECT VEGETATION; 6.6-HOUR EXPOSURES; MODERATE EXERCISE;
D O I
10.1016/j.atmosenv.2007.03.052
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Results from controlled laboratory exposures of human volunteers indicate that higher ozone (03) hourly average concentrations elicit a greater effect on hour-by-hour physiologic response (i.e., forced expiratory volume in I s [FEV1]) than lower hourly average values, which implies a nonlinear dose-response relationship. The current 8-h average human-health 03 standard is not adequate for describing this nonlinear FEV(1) hour-by-hour pattern of response. Consequently, it is recommended that physiologically consistent sigmoidally shaped dose-response models based on controlled human laboratory data be integrated into the air quality standard-setting process. The sigmoidally shaped model is continuous, does not require the identification of a population threshold concentration, and deals with plateau considerations at the high end of the distribution of exposures. For developing a consistent standard to protect human health, it is important to identify those ambient-type concentration patterns that elicit adverse human health effects. Such a standard should be ultimately based not only on spirometric response but other potentially important health impairment endpoints. Because of the paucity of experimental results that utilize ambient-type concentration regimes, additional studies are needed to create a database that uses realistic ambient-type exposures (i.e., variable concentration regimes) for human laboratory studies. The ambient-type concentration patterns that elicit an adverse health effect can be subsequently integrated into a form and level of a protective standard. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4559 / 4570
页数:12
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