4.6 Article

Biomarkers representing key aging-related biological pathways are associated with subclinical atherosclerosis and all-cause mortality: The Framingham Study

Journal

PLOS ONE
Volume 16, Issue 5, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0251308

Keywords

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Funding

  1. National Heart, Lung and Blood Institute [NO1-HC25195, HHSN268201500001I, 75N92019D00031, 2K24 HL04334, 6R01-NS 17950, R01 AG021593, 1RO1-HL64753, R01HL076784, RO1HL080124, 1R38HL143584]
  2. NIH Boston University Cardiovascular Center [N01-HV-28178]
  3. NIH [HL71039]
  4. National Institute on Aging [1R01-AG028321]
  5. Evans Medical Foundation
  6. Jay and Louis Coffman Endowment from the Department of Medicine, Boston University School of Medicine
  7. Multidisciplinary Training Program (T32) in Cardiovascular Epidemiology [5T32HL125232]

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The study findings suggest that biomarkers related to oxidative stress, telomere length shortening, endothelial dysfunction, and lower IGF-1 concentrations are associated with subclinical atherosclerosis and all-cause mortality, indicating their potential role in reflecting the aging process in community-dwelling adults.
Background Increased oxidative stress, leukocyte telomere length (LTL) shortening, endothelial dysfunction, and lower insulin-like growth factor (IGF)-1 concentrations reflect key molecular mechanisms of aging. We hypothesized that biomarkers representing these pathways are associated with measures of subclinical atherosclerosis and all-cause mortality. Methods and results We evaluated up to 2,314 Framingham Offspring Study participants (mean age 61 years, 55% women) with available biomarkers of aging: LTL, circulating concentrations of IGF-1, asymmetrical dimethylarginine (ADMA), and urinary F2-Isoprostanes indexed to urinary creatinine. We evaluated the association of each biomarker with coronary artery calcium [ln (CAC+1)] and carotid intima-media thickness (IMT). In multivariable-adjusted linear regression models, higher ADMA levels were associated with higher CAC values (beta (ADMA) per 1-SD increase 0.25; 95% confidence interval [CI] [0.11, 0.39]). Additionally, shorter LTL and lower IGF-1 values were associated with higher IMT values (beta (LTL) -0.08, 95%CI -0.14, -0.02, and beta (IGF-1) -0.04, 95%CI -0.08, -0.01, respectively). During a median follow-up of 15.5 years, 593 subjects died. In multivariable-adjusted Cox regression models, LTL and IGF-1 values were inversely associated with all-cause mortality (hazard ratios [HR] per SD increase in biomarker, 0.85, 95% CI 0.74-0.99, and 0.90, 95% CI 0.82-0.98 for LTL and IGF-1, respectively). F2-Isoprostanes and ADMA values were positively associated with all-cause mortality (HR per SD increase in biomarker, 1.15, 95% CI, 1.10-1.22, and 1.10, 95% CI, 1.02-1.20, respectively). Conclusion In our prospective community-based study, aging-related biomarkers were associated with measures of subclinical atherosclerosis cross-sectionally and with all-cause mortality prospectively, supporting the concept that these biomarkers may reflect the aging process in community-dwelling adults.

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