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Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers

Primary insomnia is often considered a disorder of 24‐hr hyperarousal. Numerous attempts have been made to investigate nocturnal heart rate (HR) and its variability (HRV) as potential pathophysiological hallmarks of altered arousal levels in insomnia, with mixed results. We have aimed to overcome so...

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Autores principales: Cosgrave, Jan, Phillips, Jessica, Haines, Ross, Foster, Russell G., Steinsaltz, David, Wulff, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577225/
https://www.ncbi.nlm.nih.gov/pubmed/33622029
http://dx.doi.org/10.1111/jsr.13278
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author Cosgrave, Jan
Phillips, Jessica
Haines, Ross
Foster, Russell G.
Steinsaltz, David
Wulff, Katharina
author_facet Cosgrave, Jan
Phillips, Jessica
Haines, Ross
Foster, Russell G.
Steinsaltz, David
Wulff, Katharina
author_sort Cosgrave, Jan
collection PubMed
description Primary insomnia is often considered a disorder of 24‐hr hyperarousal. Numerous attempts have been made to investigate nocturnal heart rate (HR) and its variability (HRV) as potential pathophysiological hallmarks of altered arousal levels in insomnia, with mixed results. We have aimed to overcome some of the pitfalls of previous studies by using a young, medication‐free, age‐ and gender‐matched population consisting of 43 students aged 18–30 years half with a subthreshold insomnia complaint. We employed at‐home ambulatory polysomnography and compared this attenuated insomnia group to a good sleeping group. The poor sleepers had significantly higher wake after sleep onset, arousal count, mean HR in all sleep stages (with the exception of Stage 1) and lower sleep efficiency. Consistent with previous research, we also found a significant group‐by‐sleep stage interaction in the prediction of nocturnal HR, highlighting the insomnia group to have a lower wake–sleep HR reduction compared to good sleepers. When restricting our analyses to insomnia with objectively determined short sleep duration, we found significantly lower standard deviation of RR intervals (SDNN; a measure of HRV) compared to good sleepers. Taken together, this lends credence to the hyperarousal model of insomnia and may at least partially explain the increased prevalence of cardiovascular morbidity and mortality observed in patients with insomnia.
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spelling pubmed-85772252021-11-15 Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers Cosgrave, Jan Phillips, Jessica Haines, Ross Foster, Russell G. Steinsaltz, David Wulff, Katharina J Sleep Res Insomnia Primary insomnia is often considered a disorder of 24‐hr hyperarousal. Numerous attempts have been made to investigate nocturnal heart rate (HR) and its variability (HRV) as potential pathophysiological hallmarks of altered arousal levels in insomnia, with mixed results. We have aimed to overcome some of the pitfalls of previous studies by using a young, medication‐free, age‐ and gender‐matched population consisting of 43 students aged 18–30 years half with a subthreshold insomnia complaint. We employed at‐home ambulatory polysomnography and compared this attenuated insomnia group to a good sleeping group. The poor sleepers had significantly higher wake after sleep onset, arousal count, mean HR in all sleep stages (with the exception of Stage 1) and lower sleep efficiency. Consistent with previous research, we also found a significant group‐by‐sleep stage interaction in the prediction of nocturnal HR, highlighting the insomnia group to have a lower wake–sleep HR reduction compared to good sleepers. When restricting our analyses to insomnia with objectively determined short sleep duration, we found significantly lower standard deviation of RR intervals (SDNN; a measure of HRV) compared to good sleepers. Taken together, this lends credence to the hyperarousal model of insomnia and may at least partially explain the increased prevalence of cardiovascular morbidity and mortality observed in patients with insomnia. John Wiley and Sons Inc. 2021-02-23 2021-08 /pmc/articles/PMC8577225/ /pubmed/33622029 http://dx.doi.org/10.1111/jsr.13278 Text en © 2021 The Authors. Journal of Sleep Research published by John Wiley & Sons Ltd on behalf of European Sleep Research Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Insomnia
Cosgrave, Jan
Phillips, Jessica
Haines, Ross
Foster, Russell G.
Steinsaltz, David
Wulff, Katharina
Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers
title Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers
title_full Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers
title_fullStr Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers
title_full_unstemmed Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers
title_short Revisiting nocturnal heart rate and heart rate variability in insomnia: A polysomnography‐based comparison of young self‐reported good and poor sleepers
title_sort revisiting nocturnal heart rate and heart rate variability in insomnia: a polysomnography‐based comparison of young self‐reported good and poor sleepers
topic Insomnia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577225/
https://www.ncbi.nlm.nih.gov/pubmed/33622029
http://dx.doi.org/10.1111/jsr.13278
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