TY - JOUR
T1 - Middle-aged men show higher sensitivity of sleep to the arousing effects of corticotropin-releasing hormone than young men
T2 - Clinical implications
AU - Vgontzas, Alexandros N.
AU - Bixler, Edward O.
AU - Wittman, Annmarie M.
AU - Zachman, Keith
AU - Lin, Hung Mo
AU - Vela-Bueno, Antonio
AU - Kales, Anthony
AU - Chrousos, George P.
PY - 2001
Y1 - 2001
N2 - The prevalence of insomnia associated with emotional stress increases markedly in middle-age. Both the top and end hormones of the hypothalamic-pituitary-adrenal axis, i.e. CRH and glucocorticoids, stimulate arousal/wakefulness and inhibit slow wave (deep) sleep in experimental animals and man. The objective of this study was to test the hypothesis that middle-age is characterized by increased sensitivity to the sleep-disturbing effects of the hypothalamic-pituitary-adrenal axis. We studied 12 healthy middle-aged (45.1 ± 4.9) and 12 healthy young (22.7 ± 2.8) men by monitoring their sleep by polysomnography for 4 consecutive nights, including in tandem i adaptation and 2 baseline nights and a night during which we administered equipotent doses of ovine CRH (1 μg/kg, iv bolus) 10 min after sleep onset. Analyses included comparisons within and between groups using multiple ANOVA and regression analysis. Although both middle-aged and young men responded to CRH with similar elevations of ACTH and cortisol, the former had significantly more wakefulness and suppression of slow wave sleep compared with baseline sleep; in contrast, the latter showed no change. Also, comparison of the change in sleep patterns from baseline to the CRH night in the young men to the respective change observed in middle-aged men showed that middle-age was associated with significantly higher wakefulness and significantly greater decrease in slow wave sleep than in young age. We conclude that middle-aged men show increased vulnerability of sleep to stress hormones, possibly resulting in impairments in the quality of sleep during periods of stress. We suggest that changes in sleep physiology associated with middle-age play a significant role in the marked increase of prevalence of insomnia in middle-age.
AB - The prevalence of insomnia associated with emotional stress increases markedly in middle-age. Both the top and end hormones of the hypothalamic-pituitary-adrenal axis, i.e. CRH and glucocorticoids, stimulate arousal/wakefulness and inhibit slow wave (deep) sleep in experimental animals and man. The objective of this study was to test the hypothesis that middle-age is characterized by increased sensitivity to the sleep-disturbing effects of the hypothalamic-pituitary-adrenal axis. We studied 12 healthy middle-aged (45.1 ± 4.9) and 12 healthy young (22.7 ± 2.8) men by monitoring their sleep by polysomnography for 4 consecutive nights, including in tandem i adaptation and 2 baseline nights and a night during which we administered equipotent doses of ovine CRH (1 μg/kg, iv bolus) 10 min after sleep onset. Analyses included comparisons within and between groups using multiple ANOVA and regression analysis. Although both middle-aged and young men responded to CRH with similar elevations of ACTH and cortisol, the former had significantly more wakefulness and suppression of slow wave sleep compared with baseline sleep; in contrast, the latter showed no change. Also, comparison of the change in sleep patterns from baseline to the CRH night in the young men to the respective change observed in middle-aged men showed that middle-age was associated with significantly higher wakefulness and significantly greater decrease in slow wave sleep than in young age. We conclude that middle-aged men show increased vulnerability of sleep to stress hormones, possibly resulting in impairments in the quality of sleep during periods of stress. We suggest that changes in sleep physiology associated with middle-age play a significant role in the marked increase of prevalence of insomnia in middle-age.
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U2 - 10.1210/jcem.86.4.7370
DO - 10.1210/jcem.86.4.7370
M3 - Article
C2 - 11297573
AN - SCOPUS:0035035002
SN - 0021-972X
VL - 86
SP - 1489
EP - 1495
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 4
ER -