1
Submitted: 5 March, 2019; Revised: 6 June, 2019
© Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society.
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Original Article
Sleep and wake are shared and transmitted between
individuals with insomnia and their bed-sharing partners
Elizabeth M. Walters
1
, Andrew J. K. Phillips
1
, Alix Mellor
1
, Kellie Hamill
1
,
Melissa M. Jenkins
2
, Peter J. Norton
1
, Donald H. Baucom
3
and
Sean P. A. Drummond
1,
*
,
1
School of Psychological Sciences and Turner Institute for Brain and Mental Health, Monash University, Melbourne, Victoria,
Australia,
2
Center for Stress and Anxiety Management, San Diego, CA and
3
Department of Psychology and Neuroscience,
University of North Carolina, Chapel Hill, NC
*Corresponding author. Sean P. A. Drummond, Monash Institute for Cognitive and Clinical Neurosciences, School of Psychological Sciences, Monash
University, 18 Innovation Walk, Clayton, Victoria 2300, Australia. Email: sean.drummond@monash.edu
Abstract
Patients with insomnia frequently report disturbing, or being disturbed by, their bedpartner. We aimed to (1) characterize how individuals with insomnia and their
bedpartners influence each other’s sleep and (2) identify characteristics predicting vulnerability to wake transmission. Fifty-two couples (aged 19–82 years), where
one individual was diagnosed with insomnia, participated. Sleep/wake patterns were monitored via actigraphy and sleep diaries for seven nights. Minute-by-minute
sleep and wake concordance (simultaneous sleep/wake epochs), number of wake transmissions received (awakenings immediately preceded by wakefulness in the
bedpartner), percent wake transmissions received (percentage of total awakenings that were transmitted), and percent of bedpartner’s wake minutes resistant to
transmission (ability to sleep through bedpartner wakefulness) were calculated. Mixed-effects modeling assessed within-couple bedtime and chronotype differences
as predictors of dyadic sleep. We described rates of sleep concordance (M
Patient
= 63.8%, M
Partner
= 65.6%), wake concordance (M
Patient
= 6.6%, M
Partner
= 6.6%), total
transmissions received (M
Patient
= 5.5, M
Partner
= 6.9 per night), percent transmissions received (M
Patient
= 18.5%, M
Partner
= 23.4% of total awakenings), and percent minutes
resistant (M
Patient
= 56.4%, M
Partner
= 58.6% of bedpartner’s wake time). Partners received wake transmissions at 1.25 times the rate of patients. Percent transmissions
received was increased in couples with concordant bedtimes and individuals with later chronotype than their bedpartner. Patterns of chronotype and bedtime
order predicting percent minutes resistant to transmission differed across the length of the rest interval. Transmission provides a novel characterization of how
bedpartners influence sleep and provide insight into mechanisms of insomnia generation and maintenance. Understanding modifiable risk factors may provide ways
to personalize insomnia treatments.
Clinical Trial: Researching Effective Sleep Treatments (Project REST), ANZCTR Registration: ACTRN12616000586415
Key words: couples; insomnia; concordance; wake transmission; relationships; sleep disorders; dyad
Statement of Significance
Recent research suggest that sleep problems in an individual can precipitate sleep problems in their bedpartner, but ways to systematically
assess this process do not exist. Here, we quantify a novel metric in bed-sharing couples comprising one individual with insomnia and
their partner: transmission of wake between bedpartners (awakenings occurring immediately after wake in the bedpartner). Partners of in-
somnia patients receive more frequent wake transmissions than those with insomnia, indicating that having a bedpartner with insomnia
is disruptive to sleep. Individual sleep timing and chronotype characteristics predict the degree of bedpartner disruption. Understanding
modifiable risk factors related to dyadic sleep has implications for preventing the development of insomnia and improving insomnia
therapies.
SLEEPJ, 2020, 1–12
doi: 10.1093/sleep/zsz206
Advance Access Publication Date: 25 September 2019
Original Article
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