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J Am Coll Cardiol, 2005; 46:344-350, doi:10.1016/j.jacc.2005.03.068
(Published online 5 July 2005). © 2005 by the American College of Cardiology Foundation |




,*
* Heart and Lung Unit, Torbay Hospital, Torquay, United Kingdom
Barts and the London Queen Mary College of Medicine and Dentistry, London, United Kingdom
Department of Cardiovascular Medicine, University of Birmingham Medical School, Birmingham, United Kingdom
Department of Physiology, University of Birmingham Medical School, Birmingham, United Kingdom
|| Department of Psychological Medicine, University of Wales College of Medicine, Cardiff, Wales, United Kingdom
¶ Department of Cardiology, University of Wales College of Medicine, Cardiff, Wales, United Kingdom
# Department of Cardiology, Great Ormond Street Hospital for Children, London, United Kingdom
Manuscript received January 24, 2005; revised manuscript received March 21, 2005, accepted March 29, 2005.
* Reprint requests and correspondence: Prof. Michael P. Frenneaux, Department of Cardiovascular Medicine, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom (Email: M.P.Frenneaux{at}bham.ac.uk).
OBJECTIVES: This study was designed to investigate the role of cortisol in stress-induced endothelial dysfunction and impaired baroreflex sensitivity (BRS) by blocking cortisol production with metyrapone before subjecting healthy volunteers to mental stress.
BACKGROUND: Mental stress raises cortisol levels and is associated with increased coronary heart disease (CHD) morbidity and mortality, especially from sudden cardiac death. It also causes endothelial dysfunction and impaired BRS.
METHODS: We measured brachial artery flow-mediated dilation (FMD), a measure of endothelial function, and BRS in 36 subjects without CHD risk factors who were then randomized in a double-blind fashion to oral metyrapone 750 mg x 2 or placebo. Five hours later we subjected subjects to mental stress and then remeasured endothelial function and BRS.
RESULTS: Prestress cortisol levels were significantly higher in the placebo group at 270.5 (30.9) nmol/l versus 89.1 (11.8) nmol/l (p = 0.01), and the increase with stress was higher at 57.9 (17.9) nmol/l versus 11.2 (2.2) nmol/l (p < 0.001). In the placebo group, compared to baseline, FMD and BRS fell significantly from 4.5% (0.7%) to 1.4% (1.1%) (p = 0.02) and 21.4 (2.3) ms/mm Hg to 16.3 (1.5) ms/mm Hg (p = 0.04), respectively. In the metyrapone group, FMD and BRS were unchanged from baseline: 4.3% (0.9%) versus 5.1% (0.8%) (p = 0.48) and 26.4 (2.9) ms/mm Hg versus 24.9 (2.6) ms/mm Hg (p = 0.62), respectively. Analysis of covariation showed a significant effect of metyrapone on change in both FMD (p = 0.009) and BRS (p = 0.024).
CONCLUSIONS: Stress-related endothelial dysfunction and BRS impairment can be prevented by blocking cortisol production with metyrapone, demonstrating a direct or facilitative role for cortisol in these phenomena and suggesting mechanisms by which stress contributes to CHD and sudden cardiac death.
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