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. 2020 Aug 12;15(8):e0237235.
doi: 10.1371/journal.pone.0237235. eCollection 2020.

Lifestyle and behavioral factors and mitochondrial DNA copy number in a diverse cohort of mid-life and older adults

Affiliations

Lifestyle and behavioral factors and mitochondrial DNA copy number in a diverse cohort of mid-life and older adults

Chirag M Vyas et al. PLoS One. .

Abstract

Mitochondrial DNA copy number (mtDNAcn) is a putative biomarker of oxidative stress and biological aging. Modifiable factors, including physical activity (PA), avoidance of heavy alcohol use and smoking, and maintaining good mental health, may reduce oxidative stress and promote healthy aging. Yet, limited data exist regarding how these factors are associated with mtDNAcn or whether age, sex or race/ethnicity moderate associations. In this cross-sectional study, we selected 391 adults (183 non-Hispanic White, 110 Black and 98 Hispanic; mean = 67 years) from the VITAL-DEP (VITamin D and OmegA-3 TriaL-Depression Endpoint Prevention) ancillary to the VITAL trial. We estimated associations between lifestyle and behavioral factors (PA, alcohol consumption, cigarette smoking and depression) and log-transformed mtDNAcn using multivariable linear regression models. MtDNAcn was not correlated with chronological age; women had ~17% higher mtDNAcn compared to men. There were no significant associations between PA measures (frequency, amount or intensity) or alcohol consumption with mtDNAcn. Cigarette smoking (per 5 pack-years) was significantly associated with mtDNAcn (percent difference = -2.9% (95% confidence interval (CI) = -5.4%, -0.4%)); a large contrast was observed among heavy vs. non-smokers (≥30 vs. 0 pack-years): percent difference = -28.5% (95% CI = -44.2%, -8.3%). The estimate of mtDNAcn was suggestively different for past vs. no depression history (percent difference = -15.1% 95% CI = -30.8%, 4.1%), but this difference was not statistically significant. The association between smoking and log-mtDNAcn varied by sex and race/ethnicity; it was stronger in men and Black participants. While chance findings cannot be excluded, results from this study support associations of smoking, but not chronological age, with mtDNAcn and suggest nuanced considerations of mtDNAcn as indicative of varying oxidative stress states vs. biological aging itself.

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Conflict of interest statement

The authors have read the journal’s policy and have the following potential competing interests: DM has received research support from Nordic Naturals. He has received honoraria for speaking from the Massachusetts General Hospital Psychiatry Academy, Harvard Blog and Peer-point Medical Education Institute, LLC. He also works with the MGH Clinical Trials Network and Institute (CTNI), which has received research funding from multiple pharmaceutical companies and NIMH. OIO receives royalties from Springer Publishing for a book on late-life depression prevention. CFR receives payment from the American Association of Geriatric Psychiatry as Editor-in-Chief of the American Journal of Geriatric Psychiatry, royalty income for intellectual property as co-inventor of the Pittsburgh Sleep Quality Index and honorarium from Merck for consultation on care pathways for insomnia. CG receives royalties from Up-to-Date. This does not alter our adherence to PLOS ONE policies on sharing data and materials. There are no patents, products in development or marketed products associated with this research to declare.

Figures

Fig 1
Fig 1. Association between cigarette smoking (per 5 pack-years) and percent differences (95% CI) in mitochondrial DNA copy number (log-transformed N/S ratio), stratified by sex and race/ethnicity.
* Estimates were calculated based on model adjusted for age (years), sex, race, education (post-college vs college or under), income (<$50,000 vs ≥ $50,000), body mass index categories (18.5–24.9, 25.0–29.9, ≥ 30 kg/m2), total physical activity (<5, 5–29.99, ≥ 30 MET-hours/week), alcohol consumption (daily vs less than frequent daily), smoking use (<30 or ≥ 30 smoking pack-years) and depression category (past but not current history of depression or prevalent depression vs no prior history of depression), multivitamin use, comorbid conditions (hypertension, diabetes and use of cholesterol lowering medication).

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