Inter-individual differences in habitual sleep timing and entrained phase of endogenous circadian rhythms of BMAL1, PER2 and PER3 mRNA in human leukocytes.

Full Abstract

STUDY

OBJECTIVES:
Individual sleep timing differs and is governed partly by circadian oscillators, which may be assessed by hormonal markers, or by clock gene expression. Clock gene expression oscillates in peripheral tissues, including leukocytes. The study objective was to determine whether the endogenous phase of these rhythms, assessed in the absence of the sleep-wake and light-dark cycle, correlates with habitual sleep-wake timing.

DESIGN:
Observational, cross-sectional.

SETTING:
Home environment and Clinical Research Center.

PARTICIPANTS:
24 healthy subjects aged 25.0 +/- 3.5 (SD) years.

MEASUREMENTS:
Actigraphy and sleep diaries were used to characterize sleep timing. Circadian rhythm phase and amplitude of plasma melatonin, cortisol, and BMAL1, PER2, and PER3 expression were assessed during a constant routine.

RESULTS:
Circadian oscillations were more robust for PER3 than for BMAL1 or PER2. Average peak timings were 6:05 for PER3, 8:06 for PER2, 15:06 for BMAL1, 4:20 for melatonin, and 10:49 for cortisol. Individual sleep-wake timing correlated with the phases of melatonin and cortisol. Individual PER3 rhythms correlated significantly with sleep-wake timing and the timing of melatonin and cortisol, but those of PER2 and BMAL1 did not reach significance. The correlation between sleep timing and PER3 expression was stronger in individuals homozygous for the variant of the PER3 polymorphism that is associated with morningness.

CONCLUSIONS:
Individual phase differences in PER3 expression during a constant routine correlate with sleep timing during entrainment. PER3 expression in leukocytes represents a useful molecular marker of the circadian processes governing sleep-wake timing.

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Author information

Author/s: Archer, Simon N (SN); Viola, Antoine U (AU); Kyriakopoulou, Vanessa (V); von Schantz, Malcolm (M); Dijk, Derk-Jan (DJ);

Affiliation: Surrey Sleep Research Centre, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK. simon.archer(-atsign-)surrey.ac.uk

Grants: BBS/B/08523 (Agency:United Kingdom Biotechnology and Biological Sciences Research Council)

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal: Sleep (Sleep), published in United States. (Language: eng)

Reference: 2008-May; vol 31 (issue 5) : pp 608-17

Dates: Created 2008/06/03; Completed 2008/07/17;

PMID: 18517031, status: MEDLINE (last retrieval date: 11/6/2008)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Adult
Circadian Rhythm - genetics
Cross-Sectional Studies
Female
Genetic Markers - genetics
Habits
Humans
Hydrocortisone - blood
Individuality

Individuality
Leukocytes - metabolism
Male
Melatonin - blood
Phenotype
Polysomnography
RNA, Messenger - genetics
Sleep - genetics
Wakefulness - genetics

Associated Chemicals: Genetic Markers (0) ; RNA, Messenger (0) ; Hydrocortisone (50-23-7) ; Melatonin (73-31-4)

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