Heart rate variability during sleep onset in patients with insomnia with or without comorbid sleep apnea
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Ma, Yan
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Brigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
Harvard Med Sch, 75 Francis St, Boston, MA USABrigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
Ma, Yan
[1
,2
]
Mullington, Janet M.
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Harvard Med Sch, 75 Francis St, Boston, MA USA
Beth Israel Deaconess Med Ctr, Dept Neurol, Sleep & Inflammatory Syst Lab, Boston, MA USABrigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
Mullington, Janet M.
[2
,3
]
Wayne, Peter M.
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机构:
Brigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
Harvard Med Sch, 75 Francis St, Boston, MA USABrigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
Wayne, Peter M.
[1
,2
]
Yeh, Gloria Y.
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机构:
Brigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
Harvard Med Sch, 75 Francis St, Boston, MA USA
Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gen Med, Boston, MA USABrigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
Yeh, Gloria Y.
[1
,2
,4
]
机构:
[1] Brigham & Womens Hosp, Osher Ctr Integrat Hlth, Div Prevent Med, Boston, MA USA
[2] Harvard Med Sch, 75 Francis St, Boston, MA USA
[3] Beth Israel Deaconess Med Ctr, Dept Neurol, Sleep & Inflammatory Syst Lab, Boston, MA USA
[4] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gen Med, Boston, MA USA
Objectives: Pre-sleep stress or hyperarousal is a known key etiological component in insomnia disorder. Despite this, physiological alterations during the sleep onset are not well-understood. In particular, insomnia and obstructive sleep apnea (OSA) are highly prevalent co-morbid conditions, where autonomic regulation may be altered. We aimed to characterize heart rate variability (HRV) during sleep onset as a potential measure of presleep hyperarousal. Methods: We described the profile of pre-sleep HRV measures and explore autonomic differences in participants with self-reported insomnia disorder (with no OSA, n = 69; with mild OSA, n = 70; with moderate or severe OSA, n = 66), compared to normal sleep controls (n = 123). Heart rate data during the sleep onset process were extracted for HRV analyses. Results: During the sleep onset process, compared to normal sleep controls, participants with insomnia had altered HRV, indicated by higher heart rate (p = 0.004), lower SDNN (p = 0.003), reduced pNN20 (p < 0.001) and pNN50 (p = 0.010) and lower powers (p < 0.001). Participants with insomnia and moderate/severe OSA may have further deteriorated HRV outcomes compared to no/mild OSA patients with insomnia but differences were not significant. Insomnia itself was associated with significantly higher heart rate, lower pNN20, and lower high frequency power even after adjustment for age, gender, BMI and OSA severity. Conclusions: Participants with insomnia had lower vagal activity during the sleep onset period, which may be compounded by OSA, reflected in higher heart rates and lower HRV. These altered heart rate dynamics may serve as a physiological biomarker for insomnia during bedtime wakefulness, or as a potential tool to evaluate the efficacy of behavioral interventions which target bedtime stress.