Biomarkers are cellular, biochemical, or molecular alterations that can be easily and non-invasively measured in human tissues and are directly or indirectly involved in the pathway of disease. Cardiovascular disease (CVD) is the leading cause of death in the United States accounting for 800,000 deaths every year. Both short- and long-term exposure to air pollution/toxic metals has been consistently associated with CVD morbidity and death in epidemiologic studies. Platelets contribute to the development of both atherosclerosis and arterial thrombosis, which are primary contributing events leading to CVD. Increased platelet counts have been suggested to mediate particulate matter (PM) effects. Platelets are anucleate, but mitochondrial DNA (mtDNA) can be easily isolated from plasma platelets. Mitochondria are highly sensitive to PM-related oxidation and, most importantly, platelets are critically dependent on energy production in mitochondria. We hypothesize that air pollutants and metals exposure may cause alteration in platelet mitochondrial DNA methylation (mtDNA) in response to exposure-induced systemic oxidation/inflammation. Platelet mtDNA methylation changes may lead to, or at a minimum reflect mitochondrial dysfunction participating directly or indirectly to the paths linking toxic exposures to CVD risk. We propose t test these hypotheses using data and biospecimens from the Normative Aging Study (NAS), a large prospective cohort of aging individuals. We have modified and adapted protocols to isolate mtDNA from plasma platelets, and successfully tested our highly time- and cost-effective approach. Plasma platelets from 700 participants will be measured at two time points separated by 4 years for mtDNA oxidative damage (8-oxo-dG), mitochondrial global content of both standard DNA methylation (5-mC) and the emerging hydroxymethylation (5-OH-mC) mark, and locus-specific methylation in a comprehensive panel of mtDNA sequences. We will determine the effects of air pollution and metals on mtDNA biomarkers (Aim 1);evaluate further association of mtDNA biomarkers with CVD risk (Aim 2);and conduct an exploratory aim (Aim 3) to determine via mediation analysis whether platelet mtDNA changes are directly or indirectly on the paths linking toxic exposures to oxidation/inflammation markers, and ultimately to CVD risk. The proposed study will be the first to characterize mechanisms in platelet mtDNA methylation related to CVD risk. The project's focus on platelets, a single pure cell population with critical roles in CVD etiology will provide ease of interpretation of epigenetic findings and thus overcome the major limitation of current epigenetic studies in large human population, which have been hampered by the use of mixed cell populations such as white blood cells or buccal cells. Because platelets can be inexpensively and non- invasively isolated from plasma, our study has high potential to generate novel risk and diagnostic biomarkers of future CVD. If we observed the hypothesized associations, we will seek funding to expand this line of research in large-scale studies in diverse populations with high risk of CVD.

Public Health Relevance

As the age of the US population increases, the number of persons dying from cardiovascular disease (CVD) is expected to rise dramatically in the coming years. Our study will be the first to prospectively characterize mechanisms of air pollution and heavy metal impact on platelet mitochondrial DNA (mtDNA) and their relation to CVD risk. By studying CVD in a large number of pre-diagnostic samples from elderly participants with two decades of follow up, our research may provide new tools to develop targeted prevention when it is most effective, i.e. in early stages or even before any subclinical symptoms are detected.

National Institute of Health (NIH)
National Institute of Environmental Health Sciences (NIEHS)
Exploratory/Developmental Grants (R21)
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Cardiovascular and Sleep Epidemiology (CASE)
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Mcallister, Kimberly A
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Harvard University
Public Health & Prev Medicine
Schools of Public Health
United States
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Janssen, Bram G; Gyselaers, Wilfried; Byun, Hyang-Min et al. (2017) Placental mitochondrial DNA and CYP1A1 gene methylation as molecular signatures for tobacco smoke exposure in pregnant women and the relevance for birth weight. J Transl Med 15:5
Janssen, Bram G; Byun, Hyang-Min; Roels, Harry A et al. (2017) Regulating role of fetal thyroid hormones on placental mitochondrial DNA methylation: epidemiological evidence from the ENVIRONAGE birth cohort study. Clin Epigenetics 9:66
Byun, Hyang-Min; Colicino, Elena; Trevisi, Letizia et al. (2016) Effects of Air Pollution and Blood Mitochondrial DNA Methylation on Markers of Heart Rate Variability. J Am Heart Assoc 5:
Byun, Hyang-Min; Benachour, Nora; Zalko, Daniel et al. (2015) Epigenetic effects of low perinatal doses of flame retardant BDE-47 on mitochondrial and nuclear genes in rat offspring. Toxicology 328:152-9
Janssen, Bram G; Byun, Hyang-Min; Gyselaers, Wilfried et al. (2015) Placental mitochondrial methylation and exposure to airborne particulate matter in the early life environment: An ENVIRONAGE birth cohort study. Epigenetics 10:536-44
Byun, Hyang-Min; Barrow, Timothy M (2015) Analysis of pollutant-induced changes in mitochondrial DNA methylation. Methods Mol Biol 1265:271-83
Baccarelli, Andrea A; Byun, Hyang-Min (2015) Platelet mitochondrial DNA methylation: a potential new marker of cardiovascular disease. Clin Epigenetics 7:44
Byun, Hyang-Min; Baccarelli, Andrea A (2014) Environmental exposure and mitochondrial epigenetics: study design and analytical challenges. Hum Genet 133:247-57