Abstract

Context:Chronic psychological stress has been associated with shorter telomeres, but the underlying mechanisms are poorly understood. One possibility is that the neuroendocrine responses to stress exposure are involved.Objective:To test the hypothesis that greater cortisol responsivity to acute stressors predicts more rapid telomere attrition.Design:We measured salivary cortisol responses to 2 challenging behavioral tasks. Leukocyte telomere length was measured at the time of mental stress testing and 3 years later.Participants:We studied 411 initially healthy men and women aged 54 to 76 years.Main outcome measure:Leukocyte telomere length.Results:Cortisol responses to this protocol were small; we divided participants into cortisol responders (n = 156) and nonresponders (n = 255) using a criterion (≥20% increase in cortisol concentration) previously shown to predict increases in cardiovascular disease risk. There was no significant association between cortisol responsivity and baseline telomere length, although cortisol responders tended to have somewhat shorter telomeres (β = −0.061; standard error, 0.049). But cortisol responders had shorter telomeres and more rapid telomere attrition than nonresponders on follow-up, after controlling statistically for age, sex, socioeconomic status, smoking, time of day of stress , and baseline telomere length (β = −0.10; standard error, 0.046; P = 0.029). The association was maintained after additional control for cardiovascular risk factors (β = −0.11; P = 0.031). The difference between cortisol responders and nonresponders was equivalent to approximately 2 years in aging.Conclusions:These findings suggest that cortisol responsivity may mediate, in part, the relationship between psychological stress and cellular aging.

Highlights

  • MethodsParticipants We analyzed data from the Heart Scan Study, a sample of 543 men and women of white European origin of the Whitehall II epidemiological cohort recruited between 2006 and 2008 to investigate physiological responsivity to mental stress testing and subclinical coronary artery disease [21]

  • Main outcome measure: Leukocyte telomere length. Cortisol responses to this protocol were small; we divided participants into cortisol responders (n = 156) and nonresponders (n = 255) using a criterion ($20% increase in cortisol concentration) previously shown to predict increases in cardiovascular disease risk

  • There was no significant association between cortisol responsivity and baseline telomere length, cortisol responders tended to have somewhat shorter telomeres (b = 20.061; standard error, 0.049)

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Summary

Methods

Participants We analyzed data from the Heart Scan Study, a sample of 543 men and women of white European origin of the Whitehall II epidemiological cohort recruited between 2006 and 2008 to investigate physiological responsivity to mental stress testing and subclinical coronary artery disease [21]. Participants were selected as having no history of coronary heart disease and no previous diagnoses or treatment of hypertension, diabetes, inflammatory diseases, or allergies. We used civil service employment grade as an indicator of socioeconomic status (SES), and recruitment was stratified to include men and women from higher, intermediate, and lower employment grades. Participants were invited for reassessment 3 years after mental stress testing (mean interval, 1087 days). Ethical approval was obtained from the University College London Hospital Committee on the Ethics of Human Research, and all participants gave signed informed consent. All procedures were carried out in accordance with approved guidelines

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