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Northwest Center for Particulate Air Pollution and Health

Jane Q. Koenig, Director
University of Washington, Seattle, WA

EPA Grant Number: R827355

2001 Progress Report
2002 Progress Report
Center sub-projects

Center Overview:

The theme of our EPA NW Center is combustion-derived fine particulate composition exposure and health effects. We are conducting research on the unique properties of fine particles in the Western states where vegetative burning dominates compared to Eastern states where sulfates dominate. Our center is conducting studies in exposure assessment and health effects, epidemiology, and toxicology. It is our hope that the Center will be a resource to be used by the citizens of the Pacific Northwest and the Western states in general. Some highlights of our EPA NW Center are: (1) increased understanding of the correlation among indoor, outdoor, personal, and center site exposures to PM; (2) establishment of the apolipoprotein-E deficient (apoE [-/-]) mouse as an appropriate model of susceptibility for air pollution studies; (3) investigation of acute and chronic effects of PM on cardiovascular health; (4) documentation of the use of exhaled breath nitric oxide as an non-invasive measure of airway inflammation in air pollution studies; and (5) development of new statistical methods regarding case crossover studies and use of source apportionment in health effects studies. Specific findings from exposure assessment show that the correlation between personal exposures and central site monitors does not vary significantly by subject population. Our studies show that an average of 74% of outdoor particles infiltrate indoors. We used a recursive model to estimate infiltration efficiency to separate personal exposure to fine PM into its indoor and ambient (outdoor) components. Our panel study in children with asthma found that outdoor-generated particles were associated with increased exhaled nitric oxide but that indoor-generated particles were not. Using a polynomial distributed lag model we calculated that PM2.5 expo-sure up to 11 hours prior to measurement of exhaled nitric oxide (eNO) was associated with increased eNO levels. Our toxicology studies using the apoE deficient mouse show a difference in toxicity among geographically spaced PM monitors within the Seattle area. The strongest association between PM2.5 and inflammatory cytokines in the lungs was with a monitor in a wood smoke impacted area. Statistical method development includes refinement of case-crossover referent assignment and use of source apportionment in health studies.







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