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Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders

Considering the marked changes in sleep and circadian rhythms across the lifespan, age may contribute to the heterogeneity in sleep-wake profiles linked to mood disorders. This study aimed to investigate the contributions of age and depression severity to sleep-wake disturbances. The Hamilton Depres...

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Autores principales: Robillard, Rébecca, Naismith, Sharon L., Smith, Kristie Leigh, Rogers, Naomi L., White, Django, Terpening, Zoe, Ip, Tony K. C., Hermens, Daniel F., Whitwell, Bradley, Scott, Elizabeth M., Hickie, Ian B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934865/
https://www.ncbi.nlm.nih.gov/pubmed/24586290
http://dx.doi.org/10.1371/journal.pone.0087763
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author Robillard, Rébecca
Naismith, Sharon L.
Smith, Kristie Leigh
Rogers, Naomi L.
White, Django
Terpening, Zoe
Ip, Tony K. C.
Hermens, Daniel F.
Whitwell, Bradley
Scott, Elizabeth M.
Hickie, Ian B.
author_facet Robillard, Rébecca
Naismith, Sharon L.
Smith, Kristie Leigh
Rogers, Naomi L.
White, Django
Terpening, Zoe
Ip, Tony K. C.
Hermens, Daniel F.
Whitwell, Bradley
Scott, Elizabeth M.
Hickie, Ian B.
author_sort Robillard, Rébecca
collection PubMed
description Considering the marked changes in sleep and circadian rhythms across the lifespan, age may contribute to the heterogeneity in sleep-wake profiles linked to mood disorders. This study aimed to investigate the contributions of age and depression severity to sleep-wake disturbances. The Hamilton Depression Rating Scale (HDRS) was administered to assess current symptoms severity in 238 persons with a history of a mood disorder between 12 and 90 years of age (y.o.). Actigraphy was recorded over five to 22 days. Regression analyses and analyses of variance [age (12–19 y.o., 20–39 y.o., 40–59 y.o., and ≥60 y.o.) by depression severity (HDRS< and ≥8)] were conducted. The 12–19 y.o. and 20–39 y.o. groups had a delayed sleep schedule and acrophase compared to all other groups. The ≥60 y.o. group had a lower rhythmicity and amplitude (p≤.006) than the 12–19 y.o. group (p≤.046). Participants with a HDRS≥8 spent longer time in bed, had later sleep offset times and had lower circadian rhythmicity than those with a HDRS<8 (p≤.036). Younger age and higher HDRS score correlated with later sleep onset and offset times, longer time in bed, higher WASO, lower sleep efficiency and later acrophase (p≤.023). Age was a significant predictor of delayed sleep and activity schedules (p≤.001). The profile of sleep-wake cycle disturbances associated with mood disorders changes with age, with prominent sleep phase delay during youth and reduced circadian strength in older persons. Conversely, disruptions in sleep consolidation seem more stable across age.
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spelling pubmed-39348652014-03-04 Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders Robillard, Rébecca Naismith, Sharon L. Smith, Kristie Leigh Rogers, Naomi L. White, Django Terpening, Zoe Ip, Tony K. C. Hermens, Daniel F. Whitwell, Bradley Scott, Elizabeth M. Hickie, Ian B. PLoS One Research Article Considering the marked changes in sleep and circadian rhythms across the lifespan, age may contribute to the heterogeneity in sleep-wake profiles linked to mood disorders. This study aimed to investigate the contributions of age and depression severity to sleep-wake disturbances. The Hamilton Depression Rating Scale (HDRS) was administered to assess current symptoms severity in 238 persons with a history of a mood disorder between 12 and 90 years of age (y.o.). Actigraphy was recorded over five to 22 days. Regression analyses and analyses of variance [age (12–19 y.o., 20–39 y.o., 40–59 y.o., and ≥60 y.o.) by depression severity (HDRS< and ≥8)] were conducted. The 12–19 y.o. and 20–39 y.o. groups had a delayed sleep schedule and acrophase compared to all other groups. The ≥60 y.o. group had a lower rhythmicity and amplitude (p≤.006) than the 12–19 y.o. group (p≤.046). Participants with a HDRS≥8 spent longer time in bed, had later sleep offset times and had lower circadian rhythmicity than those with a HDRS<8 (p≤.036). Younger age and higher HDRS score correlated with later sleep onset and offset times, longer time in bed, higher WASO, lower sleep efficiency and later acrophase (p≤.023). Age was a significant predictor of delayed sleep and activity schedules (p≤.001). The profile of sleep-wake cycle disturbances associated with mood disorders changes with age, with prominent sleep phase delay during youth and reduced circadian strength in older persons. Conversely, disruptions in sleep consolidation seem more stable across age. Public Library of Science 2014-02-25 /pmc/articles/PMC3934865/ /pubmed/24586290 http://dx.doi.org/10.1371/journal.pone.0087763 Text en © 2014 Robillard et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Robillard, Rébecca
Naismith, Sharon L.
Smith, Kristie Leigh
Rogers, Naomi L.
White, Django
Terpening, Zoe
Ip, Tony K. C.
Hermens, Daniel F.
Whitwell, Bradley
Scott, Elizabeth M.
Hickie, Ian B.
Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders
title Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders
title_full Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders
title_fullStr Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders
title_full_unstemmed Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders
title_short Sleep-Wake Cycle in Young and Older Persons with a Lifetime History of Mood Disorders
title_sort sleep-wake cycle in young and older persons with a lifetime history of mood disorders
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934865/
https://www.ncbi.nlm.nih.gov/pubmed/24586290
http://dx.doi.org/10.1371/journal.pone.0087763
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