RESUMEN
Little is known about the impacts of specific chemical components on cardiovascular hospitalizations. We examined the relationships of PM2.5 chemical composition and daily hospitalizations for cardiovascular disease in 184 Chinese cities. Acute PM2.5 chemical composition exposures were linked to higher cardiovascular disease hospitalizations on the same day and the percentage change of cardiovascular admission was the highest at 1.76% (95% CI, 1.36-2.16%) per interquartile range increase in BC, followed by 1.07% (0.72-1.43%) for SO42-, 1.04% (0.63-1.46%) for NH4+, 0.99% (0.55-1.43%) for NO3-, 0.83% (0.50-1.17%) for OM, and 0.80% (0.34%-1.26%) for Cl-. Similar findings were observed for all cause-specific major cardiovascular diseases, except for heart rhythm disturbances. Short-term exposures to PM2.5 chemical composition were related to higher admissions and showed diverse impacts on major cardiovascular diseases.
RESUMEN
Ambient fine particulate matter (PM2.5) is associated with numerous health complications, yet the specific PM2.5 chemical components and their emission sources contributing to these health outcomes are understudied. Our study analyzes the chemical composition of PM2.5 collected from five distinct locations at urban, roadside and rural environments in midwestern region of the United States, and associates them with five acellular oxidative potential (OP) endpoints of water-soluble PM2.5. Redox-active metals (i.e., Cu, Fe, and Mn) and carbonaceous species were correlated with most OP endpoints, suggesting their significant role in OP. We conducted a source apportionment analysis using positive matrix factorization (PMF) and found a strong disparity in the contribution of various emission sources to PM2.5 mass vs. OP. Regional secondary sources and combustion-related aerosols contributed significantly (> 75 % in total) to PM2.5 mass, but showed weaker contribution (43-69 %) to OP. Local sources such as parking emissions, industrial emissions, and agricultural activities, though accounting marginally to PM2.5 mass (< 10 % for each), significantly contributed to various OP endpoints (10-50 %). Our results demonstrate that the sources contributing to PM2.5 mass and health effects are not necessarily same, emphasizing the need for an improved air quality management strategy utilizing more health-relevant PM2.5 indicators.
RESUMEN
Paternal exposure to environmental risk factors influences the offspring health. This study aimed to evaluate the association between paternal air pollution exposure mediated by sperm DNA methylation and adverse birth outcomes in offspring. We recruited 1607 fertile men and their partners from 2014 to 2016 and collected semen samples to detect sperm DNA methylation. Multivariate linear regression and weighted quantile sum regression models were used to assess the associations between paternal air pollution exposure and offspring birth outcomes. A critical exposure window was identified. Reduced representation bisulfite sequencing was used to detect sperm DNA methylation. The results demonstrated that high paternal exposure to PM2.5 (ß = -211.31, 95% CI: (-386.37, -36.24)), PM10 (ß = -178.20, 95% CI: (-277.13, -79.27)), and NO2 (ß = -84.22, 95% CI: (-165.86, -2.57)) was negatively associated with offspring's birthweight, especially in boys. Additionally, an early exposure window of 15-69 days before fertilization was recognized to be the key exposure window, which increased the risk of low birth weight and small for gestational age. Furthermore, paternal co-exposure to six air pollutants contributed to lower birthweight (ß = -51.91, 95% CI: (-92.72, -11.10)) and shorter gestational age (ß = -1.72, 95% CI: (-3.26, -0.17)) and PM2.5 was the most weighted pollutant. Paternal air pollution exposure resulted in 10,328 differentially methylated regions and the IGF2R gene was the key gene involved in the epigenetic process. These differentially methylated genes were predominantly associated with protein binding, transcriptional regulation, and DNA templating. These findings indicate that spermatogenesis is a susceptible window during which paternal exposure to air pollution affects sperm DNA methylation and the birth outcomes of offspring.