Associations between long-term exposure to PM2.5 component species and blood DNA methylation age in the elderly: The VA normative aging study

Environ Int. 2017 May:102:57-65. doi: 10.1016/j.envint.2016.12.024. Epub 2017 Mar 9.

Abstract

Background: Long-term PM2.5 exposure and aging have been implicated in multiple shared diseases; studying their relationship is a promising strategy to further understand the adverse impact of PM2.5 on human health.

Objective: We assessed the relationship of major PM2.5 component species (ammonium, elemental carbon, organic carbon, nitrate, and sulfate) with Horvath and Hannum DNA methylation (DNAm) age, two DNA methylation-based predictors of chronological age.

Methods: This analysis included 552 participants from the Normative Aging Study with multiple visits between 2000 and 2011 (n=940 visits). We estimated 1-year PM2.5 species levels at participants' addresses using the GEOS-chem transport model. Blood DNAm-age was calculated using CpG sites on the Illumina HumanMethylation450 BeadChip. We fit linear mixed-effects models, controlling for PM2.5 mass and lifestyle/environmental factors as fixed effects, with the adaptive LASSO penalty to identify PM2.5 species associated with DNAm-age.

Results: Sulfate and ammonium were selected by the LASSO in the Horvath DNAm-age models. In a fully-adjusted multiple-species model, interquartile range increases in both 1-year sulfate (95%CI: 0.28, 0.74, P<0.0001) and ammonium (95%CI: 0.02, 0.70, P=0.04) levels were associated with at least a 0.36-year increase in Horvath DNAm-age. No PM2.5 species were selected by the LASSO in the Hannum DNAm-age models. Our findings persisted in sensitivity analyses including only visits with 1-year PM2.5 levels within US EPA national ambient air quality standards.

Conclusion: Our results demonstrate that sulfate and ammonium were most associated with Horvath DNAm-age and suggest that DNAm-age measures differ in their sensitivity to ambient particle exposures and potentially disease.

Keywords: DNA methylation age; Epigenetics; Long-term exposure; Particulate matter 2.5.

MeSH terms

  • Aged
  • Aging / blood*
  • Aging / genetics
  • Air Pollutants / analysis*
  • Air Pollutants / toxicity
  • DNA / blood*
  • DNA Methylation / drug effects*
  • Environmental Monitoring / methods*
  • Female
  • Humans
  • Inhalation Exposure / analysis
  • Male
  • Particle Size
  • Particulate Matter / analysis*
  • Particulate Matter / toxicity
  • United States
  • United States Environmental Protection Agency

Substances

  • Air Pollutants
  • Particulate Matter
  • DNA