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Robust stability of melatonin circadian phase, sleep metrics, and chronotype across months in young adults living in real-world settings

  • Andrew W. McHill
  • , Akane Sano
  • , Cassie J. Hilditch
  • , Laura K. Barger
  • , Charles A. Czeisler
  • , Rosalind Picard
  • , Elizabeth B. Klerman

Research output: Contribution to journalArticlepeer-review

Abstract

Appropriate synchronization of the timing of behaviors with the circadian clock and adequate sleep are both important for almost every physiological process. The timing of the circadian clock relative to social (ie, local) clock time and the timing of sleep can vary greatly among individuals. Whether the timing of these processes is stable within an individual is not well-understood. We examined the stability of circadian-controlled melatonin timing, sleep timing, and their interaction across ~ 100 days in 15 students at a single university. At three time points ~ 35-days apart, circadian timing was determined from the dim-light melatonin onset (DLMO). Sleep behaviors (timing and duration) and chronotype (ie, mid-sleep time on free days corrected for sleep loss on school/work days) were determined via actigraphy and analyzed in ~ 1-month bins. Melatonin timing was stable, with an almost perfect relationship strength as determined via intraclass correlation coefficients ([ICC]=0.85); average DLMO timing across all participants only changed from the first month by 21 minutes in month 2 and 5 minutes in month 3. Sleep behaviors also demonstrated high stability, with ICC relationship strengths ranging from substantial to almost perfect (ICCs = 0.65-0.85). Average DLMO was significantly associated with average chronotype (r2 = 0.53, P <.01), with chronotype displaying substantial stability across months (ICC = 0.61). These findings of a robust stability in melatonin timing and sleep behaviors in young adults living in real-world settings holds promise for a better understanding of the reliability of previous cross-sectional reports and for the future individualized strategies to combat circadian-associated disease and impaired safety (ie, “chronomedicine”).

Original languageEnglish (US)
Article numbere12720
JournalJournal of pineal research
Volume70
Issue number3
DOIs
StatePublished - Apr 1 2021

Funding

We thank the participants and Center for Clinical Investigation staff for their support in conducting these studies. This work was funded by the National Institutes of Health (Dr McHill was supported in part by K01HL146992, F32DK107146, and T32HL007901; Drs. Barger and Czeisler were supported in part by R01OH011773 and Dr Barger by R01AG044416; Dr Klerman was supported in part by K24HL105664, R01HL114088, R01GM105018, R01HL128538, and P01AG009975; Drs. Sano and Picard were supported in part by R01GM105018; NIH grant 1UL1 TR001102-01, 8UL1TR000170-05, UL1 RR 025758, Harvard Clinical and Translational Science Center, from the National Center for Advancing Translational Science).

FundersFunder number
Author National Institutes of Health National Institutes of Health National Institutes of Health National Institutes of Health The Bev Hartig Huntington's Disease Foundation National Institutes of HealthF32DK107146, P01AG009975, T32HL007901, R01HL114088, 8UL1TR000170-05, R01AG044416, K24HL105664, R01GM105018, 1UL1 TR001102-01, UL1 RR 025758, R01HL128538, K01HL146992
National Institute for Occupational Safety and HealthR01OH011773
National Center for Advancing Translational Sciences
Harvard Catalyst

    Keywords

    • Circadian rhythm/ physiology
    • Human
    • Melatonin / biosynthesis
    • Melatonin / metabolism
    • Saliva / metabolism
    • Sleep / physiology
    • Time factors

    ASJC Scopus subject areas

    • Endocrinology

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