4.7 Article

Emulating causal dose-response relations between air pollutants and mortality in the Medicare population

期刊

ENVIRONMENTAL HEALTH
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12940-021-00742-x

关键词

Air pollution; Chronic exposures; Mortality; Causal modeling; Does-response relations

资金

  1. United States Environmental Protection Agency (US EPA) [RD-8358720, RD-83587201-0]
  2. National Institutes of Health (NIH) [ES-000002, R01 ES024332-01, R01 MD012769, R01 ES028033, R21 ES024012, 1R01AG060232-01A1, 1R01ES030616, 1R01AG066793-01R01]
  3. Health Effects Institute (HEI) [4953-RFA14-3/16-4]
  4. Alfred P. Sloan Foundation [G-2020-13946]
  5. Harvard University Climate Change Solutions Fund

向作者/读者索取更多资源

This study explored the causal dose-response relations between chronic exposures to PM2.5, O3, NO2 and all-cause mortality using national Medicare cohort data from 2000 to 2016. The study found that higher levels of PM2.5, O3, and NO2 were causally associated with greater risk of mortality, with PM2.5 posing the greatest risk. A decile binning approach was proposed to make the inverse probability weights robust against outliers and provide more accurate estimates for continuous exposures. The study's findings have significant implications for reviewing national air quality standards and estimating the potential impact of reducing air pollution on early deaths.
Background Fine particulate matter (PM2.5), ozone (O-3), 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. Methods Using national Medicare cohort during 2000-2016, we simultaneously emulated causal D-R relations between chronic exposures to fine particulate matter (PM2.5), ozone (O-3), 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. Results Assuming the causal framework was valid, we found that higher levels of PM2.5, O-3, 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 O-3, 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). Conclusions This 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.

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