Research Article: Obstructive Sleep Apnea Alters Sleep Stage Transition Dynamics

Date Published: June 28, 2010

Publisher: Public Library of Science

Author(s): Matt T. Bianchi, Sydney S. Cash, Joseph Mietus, Chung-Kang Peng, Robert Thomas, Pedro Antonio Valdes-Sosa. http://doi.org/10.1371/journal.pone.0011356

Abstract: Enhanced characterization of sleep architecture, compared with routine polysomnographic metrics such as stage percentages and sleep efficiency, may improve the predictive phenotyping of fragmented sleep. One approach involves using stage transition analysis to characterize sleep continuity.

We analyzed hypnograms from Sleep Heart Health Study (SHHS) participants using the following stage designations: wake after sleep onset (WASO), non-rapid eye movement (NREM) sleep, and REM sleep. We show that individual patient hypnograms contain insufficient number of bouts to adequately describe the transition kinetics, necessitating pooling of data. We compared a control group of individuals free of medications, obstructive sleep apnea (OSA), medical co-morbidities, or sleepiness (n = 374) with mild (n = 496) or severe OSA (n = 338). WASO, REM sleep, and NREM sleep bout durations exhibited multi-exponential temporal dynamics. The presence of OSA accelerated the “decay” rate of NREM and REM sleep bouts, resulting in instability manifesting as shorter bouts and increased number of stage transitions. For WASO bouts, previously attributed to a power law process, a multi-exponential decay described the data well. Simulations demonstrated that a multi-exponential process can mimic a power law distribution.

OSA alters sleep architecture dynamics by decreasing the temporal stability of NREM and REM sleep bouts. Multi-exponential fitting is superior to routine mono-exponential fitting, and may thus provide improved predictive metrics of sleep continuity. However, because a single night of sleep contains insufficient transitions to characterize these dynamics, extended monitoring of sleep, probably at home, would be necessary for individualized clinical application.

Partial Text: Numerous endogenous and exogenous factors influence whether sleep or wake is achieved, how long a given state is maintained, and the reasons sleep architecture may become fragmented [1], [2], [3], [4]. Much effort has been invested in attempts to correlate various polysomnogram (PSG) metrics with daytime symptoms, with the goal of understanding (and promoting) those aspects of sleep that contribute most to its recuperative properties. However, correlations between daytime sleepiness and PSG metrics are not always straightforward, due in part to inter-subject variability, the subjective nature of the clinical complaints, and variations in an individual’s tolerance to sleep disruption. The commonly employed Epworth Sleepiness Scale (ESS), for example, correlates with subjective complaints of sleepiness but not with objective measures obtained from Multiple Sleep Latency Tests [5], [6].

This study complements and extends previous work on the sleep-wake dynamics in several respects. First, sleep-wake state transition probabilities are more complex than previously recognized. The temporal stability of NREM and REM sleep clearly requires more than a single-exponential function to describe the bout distributions [19], [20], [23]. Second, our simulations show that multi-exponential distributions may mimic a power law distribution, the typical function used to describe wake bout durations[19], [20], [22]. Third, we demonstrate that one night of data is not an adequate sample of sleep-wake transitions to assess transition dynamics statistically using this distribution fitting method. Finally, we show that sleep fragmentation seen in OSA involves accelerating the rate of “decay” of NREM and REM sleep bout durations.

Source:

http://doi.org/10.1371/journal.pone.0011356