Association between urinary excretion of cortisol and markers of oxidatively damaged DNA and RNA in humans

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Abstract

Chronic psychological stress is associated with accelerated aging, but the underlying biological mechanisms are not known. Prolonged elevations of the stress hormone cortisol is suspected to play a critical role. Through its actions, cortisol may potentially induce oxidatively generated damage to cellular constituents such as DNA and RNA, a phenomenon which has been implicated in aging processes. We investigated the relationship between 24 h excretion of urinary cortisol and markers of oxidatively generated DNA and RNA damage, 8-oxo-7,8-dihydro-2′-deoxyguanosine and 8-oxo-7,8-dihydroguanosine, in a sample of 220 elderly men and women (age 65 - 83 years). We found a robust association between the excretion of cortisol and the oxidation markers (R2 = 0.15, P<0.001 for both markers). Individuals in the highest quartile of cortisol excretion had a 57% and 61% higher median excretion of the DNA and RNA oxidation marker, respectively, than individuals in the lowest quartile. The finding adds support to the hypothesis that cortisol-induced damage to DNA/RNA is an explanatory factor in the complex relation between stress, aging and disease. © 2011 Joergensen et al.

Figures

  • Table 1. Demographical, clinical and biochemical characteristics of the cohort.
  • Figure 1. 24 h urinary excretion of cortisol vs markers of nucleic acid oxidation. A: Scatterplot of log-transformed 8-oxodG and 8-oxoGuo values vs 24 h cortisol excretion. B: Median nucleic acid excretion vs quartiles of cortisol excretion. Median 8-oxodG and 8-oxoGuo is 57% and 61% percent higher, respectively, in individuals in the highest vs individuals in the lowest cortisol excretion quartile. doi:10.1371/journal.pone.0020795.g001
  • Table 2. Multivariate regression analysis.

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CITATION STYLE

APA

Joergensen, A., Broedbaek, K., Weimann, A., Semba, R. D., Ferrucci, L., Joergensen, M. B., & Poulsen, H. E. (2011). Association between urinary excretion of cortisol and markers of oxidatively damaged DNA and RNA in humans. PLoS ONE, 6(6). https://doi.org/10.1371/journal.pone.0020795

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