Key result
Air pollution and bio-aerosol exposure are linked to impaired microvascular function and increased systemic inflammation.
Observational (n=48)
To explore associations of exposure to ambient and indoor air particulate and bio-aerosol pollutants with cardiovascular and respiratory disease markers, we utilized seven repeated measurements from 48 elderly subjects participating in a 4-week home air filtration study. Microvascular function (MVF), lung function, blood leukocyte counts, monocyte adhesion molecule expression, C-reactive protein, Clara cell protein (CC16) and surfactant protein-D (SPD) were examined in relation to exposure preceding each measurement. Exposure assessment included 48-h urban background monitoring of PM10, PM2.5 and particle number concentration (PNC), weekly measurements of PM2.5 in living- and bedroom, 24-h measurements of indoor PNC three times, and bio-aerosol components in settled dust on a 2-week basis. Statistically significant inverse associations included: MVF with outdoor PNC; granulocyte counts with PM2.5; CD31 expression with dust fungi; SPD with dust endotoxin. Significant positive associations included: MVF with dust bacteria; monocyte expression of CD11 with PM2.5 in the bedroom and dust bacteria and endotoxin, CD31 expression with dust serine protease; serum CC16 with dust NAGase. Multiple comparisons demand cautious interpretation of results, which suggest that outdoor PNC have adverse effects on MVF, and outdoor and indoor PM2.5 and bio-aerosols are associated with markers of inflammation and lung cell integrity.
No takes yet. Share an insight, caveat, or question.
Karottki et al. (2015) reported an observational. Exposure to ambient and indoor air particulate and bio-aerosol pollutants was evaluated on Cardiovascular and respiratory disease markers (MVF, lung function, blood leukocyte counts, monocyte adhesion molecule expression, C-reactive protein, CC16, SPD). Exposure to outdoor particle number concentrations, PM2.5, and bio-aerosols were significantly associated with adverse microvascular function and markers of inflammation and lung cell integrity.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: