Environmental Health | |
Emulating causal dose-response relations between air pollutants and mortality in the Medicare population | |
Francesca Dominici1  Yaguang Wei2  Mahdieh Danesh Yazdi2  Antonella Zanobetti2  Joel Schwartz3  Weeberb J. Requia4  Qian Di5  | |
[1] Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA, USA;Department of Environmental Health, Harvard T. H. Chan School of Public Health, Landmark Center 4th West, 401 Park Drive, 02215, Boston, MA, USA;Department of Environmental Health, Harvard T. H. Chan School of Public Health, Landmark Center 4th West, 401 Park Drive, 02215, Boston, MA, USA;Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, MA, USA;School of Public Policy and Government, Fundação Getúlio Vargas, Brasília, Distrito Federal, Brazil;Vanke School of Public Health, Tsinghua University, Beijing, China; | |
关键词: Air pollution; Chronic exposures; Mortality; Causal modeling; Does-response relations; | |
DOI : 10.1186/s12940-021-00742-x | |
来源: Springer | |
【 摘 要 】
BackgroundFine particulate matter (PM2.5), ozone (O3), and nitrogen dioxide (NO2) are major air pollutants that pose considerable threats to human health. However, what has been mostly missing in air pollution epidemiology is causal dose-response (D-R) relations between those exposures and mortality. Such causal D-R relations can provide profound implications in predicting health impact at a target level of air pollution concentration.MethodsUsing national Medicare cohort during 2000–2016, we simultaneously emulated causal D-R relations between chronic exposures to fine particulate matter (PM2.5), ozone (O3), and nitrogen dioxide (NO2) and all-cause mortality. To relax the contentious assumptions of inverse probability weighting for continuous exposures, including distributional form of the exposure and heteroscedasticity, we proposed a decile binning approach which divided each exposure into ten equal-sized groups by deciles, treated the lowest decile group as reference, and estimated the effects for the other groups. Binning continuous exposures also makes the inverse probability weights robust against outliers.ResultsAssuming the causal framework was valid, we found that higher levels of PM2.5, O3, and NO2 were causally associated with greater risk of mortality and that PM2.5 posed the greatest risk. For PM2.5, the relative risk (RR) of mortality monotonically increased from the 2nd (RR, 1.022; 95% confidence interval [CI], 1.018–1.025) to the 10th decile group (RR, 1.207; 95% CI, 1.203–1.210); for O3, the RR increased from the 2nd (RR, 1.050; 95% CI, 1.047–1.053) to the 9th decile group (RR, 1.107; 95% CI, 1.104–1.110); for NO2, the DR curve wiggled at low levels and started rising from the 6th (RR, 1.005; 95% CI, 1.002–1.018) till the highest decile group (RR, 1.024; 95% CI, 1.021–1.027).ConclusionsThis study provided more robust evidence of the causal relations between air pollution exposures and mortality. The emulated causal D-R relations provided significant implications for reviewing the national air quality standards, as they inferred the number of potential early deaths prevented if air pollutants were reduced to specific levels; for example, lowering each air pollutant concentration from the 70th to 60th percentiles would prevent 65,935 early deaths per year.
【 授权许可】
CC BY
【 预 览 】
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RO202107069235770ZK.pdf | 976KB | download |