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Delayed sleep phase cases and controls
BACKGROUND: Delayed sleep phase disorder (DSPD) is a condition in which patients have difficulty falling asleep before the early morning hours and commonly have trouble awakening before late morning or even early afternoon. Several studies have suggested that variations in habitual bedtime are 40–50...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391143/ https://www.ncbi.nlm.nih.gov/pubmed/18445295 http://dx.doi.org/10.1186/1740-3391-6-6 |
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author | Kripke, Daniel F Rex, Katharine M Ancoli-Israel, Sonia Nievergelt, Caroline M Klimecki, Walt Kelsoe, John R |
author_facet | Kripke, Daniel F Rex, Katharine M Ancoli-Israel, Sonia Nievergelt, Caroline M Klimecki, Walt Kelsoe, John R |
author_sort | Kripke, Daniel F |
collection | PubMed |
description | BACKGROUND: Delayed sleep phase disorder (DSPD) is a condition in which patients have difficulty falling asleep before the early morning hours and commonly have trouble awakening before late morning or even early afternoon. Several studies have suggested that variations in habitual bedtime are 40–50% heritable. METHODS: We recruited a case series of 205 participants, along with 221 controls (DSPD-C) with normal sleep, roughly matched for age, gender, and ancestry. A representative sample of San Diego adults recruited some years before was already available to confirm the control group. Both DSPD and DSPD-C provided blood or saliva samples for DNA and completed extensive questionnaires about sleep habits, sleep history, family history, sleep quality, morningness-eveningness traits, depression, mania, and seasonality of symptoms. The DSPD group wore wrist actigraphs for a median of 13.2 days. The representative sample collected previously had undergone actigraphic recordings, from which 48 hours of data were generally available. RESULTS: The DSPD and DSPD-C samples showed almost no overlap on morningness-eveningness scores. DSPD cases went to bed and arose about 3 hours later than the DSPD-C and the representative sample. DSPD cases reported more difficulties with sleep, poorer sleep quality, and more depression, but there was no significant difference in a history of mania. DSPD cases reported more family history of late bedtimes, but female DSPD reported that their fathers' bedtimes were later than the fathers of male DSPD. CONCLUSION: These results indicate a DSPD phenotype is familial and associated with unipolar depression. |
format | Text |
id | pubmed-2391143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23911432008-05-22 Delayed sleep phase cases and controls Kripke, Daniel F Rex, Katharine M Ancoli-Israel, Sonia Nievergelt, Caroline M Klimecki, Walt Kelsoe, John R J Circadian Rhythms Research BACKGROUND: Delayed sleep phase disorder (DSPD) is a condition in which patients have difficulty falling asleep before the early morning hours and commonly have trouble awakening before late morning or even early afternoon. Several studies have suggested that variations in habitual bedtime are 40–50% heritable. METHODS: We recruited a case series of 205 participants, along with 221 controls (DSPD-C) with normal sleep, roughly matched for age, gender, and ancestry. A representative sample of San Diego adults recruited some years before was already available to confirm the control group. Both DSPD and DSPD-C provided blood or saliva samples for DNA and completed extensive questionnaires about sleep habits, sleep history, family history, sleep quality, morningness-eveningness traits, depression, mania, and seasonality of symptoms. The DSPD group wore wrist actigraphs for a median of 13.2 days. The representative sample collected previously had undergone actigraphic recordings, from which 48 hours of data were generally available. RESULTS: The DSPD and DSPD-C samples showed almost no overlap on morningness-eveningness scores. DSPD cases went to bed and arose about 3 hours later than the DSPD-C and the representative sample. DSPD cases reported more difficulties with sleep, poorer sleep quality, and more depression, but there was no significant difference in a history of mania. DSPD cases reported more family history of late bedtimes, but female DSPD reported that their fathers' bedtimes were later than the fathers of male DSPD. CONCLUSION: These results indicate a DSPD phenotype is familial and associated with unipolar depression. BioMed Central 2008-04-29 /pmc/articles/PMC2391143/ /pubmed/18445295 http://dx.doi.org/10.1186/1740-3391-6-6 Text en Copyright © 2008 Kripke et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kripke, Daniel F Rex, Katharine M Ancoli-Israel, Sonia Nievergelt, Caroline M Klimecki, Walt Kelsoe, John R Delayed sleep phase cases and controls |
title | Delayed sleep phase cases and controls |
title_full | Delayed sleep phase cases and controls |
title_fullStr | Delayed sleep phase cases and controls |
title_full_unstemmed | Delayed sleep phase cases and controls |
title_short | Delayed sleep phase cases and controls |
title_sort | delayed sleep phase cases and controls |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391143/ https://www.ncbi.nlm.nih.gov/pubmed/18445295 http://dx.doi.org/10.1186/1740-3391-6-6 |
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