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Effects of late‐night short‐sleep on in‐home polysomnography: relation to adult age and sex
Author(s) -
Åkerstedt Torbjörn,
Lekander Mats,
Nilsonne Gustav,
Tamm Sandra,
D'onofrio Paolo,
Kecklund Göran,
Fischer Håkan,
Schwarz Johanna
Publication year - 2018
Publication title -
journal of sleep research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.297
H-Index - 117
eISSN - 1365-2869
pISSN - 0962-1105
DOI - 10.1111/jsr.12626
Subject(s) - sleep (system call) , bedtime , polysomnography , rapid eye movement sleep , psychology , slow wave sleep , medicine , sleep onset , audiology , eye movement , insomnia , electroencephalography , ophthalmology , psychiatry , apnea , computer science , operating system
Summary Bedtime is frequently delayed by many factors in life, and a homeostatic response to the delay may compensate partly for increased time awake and shortened sleep. Because sleep becomes shorter with age and women complain of disturbed sleep more often than men, age and sex differences in the homeostatic response to a delayed bedtime may modify the homeostatic response. The purpose of the present study was to investigate the effect of late‐night short‐sleep (3 h with awakening at about 07:00 hours) on in‐home recorded sleep in men and women in two age groups (20–30 and 65–75 years). Results ( N  = 59) showed that late‐night short‐sleep was associated with an increase in percentage of N3 sleep and a decrease in percentage of rapid eye movement sleep, as well as decreases in several measures of sleep discontinuity and rapid eye movement density. Men showed a smaller decrease in percentage of rapid eye movement sleep than women in response to late‐night short‐sleep, as did older individuals of both sexes compared with younger. Older men showed a weaker percentage of N3 sleep in response to late‐night short‐sleep than younger men. In general, men showed a greater percentage of rapid eye movement sleep and a lower percentage of N3 sleep than women, and older individuals showed a lower percentage of N3 sleep than younger. In particular, older men showed very low levels of percentage of N3 sleep. We conclude that older males show less of a homeostatic response to late‐night short‐sleep. This may be an indication of impaired capacity for recovery in older men. Future studies should investigate if this pattern can be linked to gender‐associated differences in morbidity and mortality.

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