SLEEP 2011 Abstract Supplement
SLEEP 2011 Abstract Supplement
SLEEP 2011 Abstract Supplement
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B. Clinical Sleep Science X. Normal Physiology of Sleep and Normal Variants<br />
0769<br />
TRACKING THE DYNAMICS OF THE EFFECTIVENESS OF<br />
<strong>SLEEP</strong><br />
Thomas RJ, Wood C<br />
Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA<br />
Introduction: Sleep physiology and pathology can be tracked by several<br />
methods-such as multiple nights of polysomnography, oximetry,<br />
and actigraphy. A new method of estimating sleep quality is the ECGspectrogram,<br />
where high frequency cardiopulmonary coupling is the<br />
biomarker of effective and restorative sleep. This biomarker associates<br />
strongly with relative rather than absolute delta power, periods of stable<br />
breathing, strong sinus arrhythmia, and blood pressure dipping. The M1<br />
(Embla) is a device with multi-night recording capability for actigraphy,<br />
ECG and body position.<br />
Methods: 2 weeks of nightly recordings with the M1 were obtained<br />
from 5 healthy adult subjects (age range 22-32, 2 female) screened with<br />
polysomnography to exclude sleep apnea, and one 58-year old male<br />
with sleep apnea. Summary metrics and intra-class coefficients (ICC)<br />
were calculated. Data from 10 subjects (each) with and without sleep<br />
apnea are expected to be available for the meeting. Sleep periods were<br />
estimated from actigraphy.<br />
Results: Analysis of variance showed that within individual night-tonight<br />
variability was not, but variability between subjects were, statistically<br />
significant. With just 6 subjects, the ICC for high, low and very low<br />
frequency % (of estimated sleep period) and duration were, respectively:<br />
0.41, 0.44, 0.13, 0.32, 0.08, and 0.18<br />
Conclusion: Sleep quality can be readily tracked across multiple nights<br />
using the ECG-spectrogram. Intra-individual variability of high frequency<br />
coupling is relatively low, and may represent a stable phenotype.<br />
Effects of sleep therapies could be assessed in a non-intrusive and costeffective<br />
manner.<br />
Support (If Any): NIH/NHLBI RC1 HL099749-01<br />
0770<br />
STABILITY AND REPRODUCIBILITY OF <strong>SLEEP</strong>INESS AND<br />
<strong>SLEEP</strong> PROBLEM PHENOTYPES OVER 4-YEAR INTERVALS<br />
IN THE WISCONSIN <strong>SLEEP</strong> COHORT STUDY<br />
Finn L 1 , Stubbs M 1 , Mignot E 2 , Peppard PE 1<br />
1<br />
Population Health Sciences, University of Wisconsin, Madison, WI,<br />
USA, 2 Stanford University, Palo Alto, CA, USA<br />
Introduction: It is not clear whether sleep-related characteristics—including<br />
objective and subjective sleepiness, insomnia symptoms, and<br />
symptoms associated with narcolepsy—represent “stable phenotypes”<br />
in generally healthy populations unselected on clinical features. To investigate<br />
stability of these sleep-related phenotypes, we examine longerterm<br />
(4-year) consistency of these characteristics in Wisconsin Sleep<br />
Cohort Study participants.<br />
Methods: The Wisconsin Sleep Cohort sample comprises 1524 subjects<br />
(45% female, 33-71 years old) who had baseline in-laboratory sleep<br />
evaluations and sleep-health interviews. Subjects have repeat studies at<br />
4-year intervals. To examine propensity to fall asleep, we used a subset<br />
of 440 subjects who underwent Multiple Sleep Latency Tests (MSLT)<br />
and completed the Epworth Sleepiness Scales (ESS) twice in a 4-year<br />
period. In addition, an overlapping subset of 841 subjects completed<br />
sleep-health interviews assessing narcolepsy and insomnia symptoms,<br />
also at 4-year intervals. We created binary categorizations of the sleep<br />
variables according to standard criteria (e.g., MSLT