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Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study

OBJECTIVES: To examine the associations between self‐reported nighttime sleep duration and daytime sleep and incident heart failure (HF) in men with and without preexisting cardiovascular disease (CVD). DESIGN: Population‐based prospective study. SETTING: General practices in 24 British towns. PARTI...

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Autores principales: Wannamethee, S. Goya, Papacosta, Olia, Lennon, Lucy, Whincup, Peter H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031211/
https://www.ncbi.nlm.nih.gov/pubmed/27351127
http://dx.doi.org/10.1111/jgs.14255
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author Wannamethee, S. Goya
Papacosta, Olia
Lennon, Lucy
Whincup, Peter H.
author_facet Wannamethee, S. Goya
Papacosta, Olia
Lennon, Lucy
Whincup, Peter H.
author_sort Wannamethee, S. Goya
collection PubMed
description OBJECTIVES: To examine the associations between self‐reported nighttime sleep duration and daytime sleep and incident heart failure (HF) in men with and without preexisting cardiovascular disease (CVD). DESIGN: Population‐based prospective study. SETTING: General practices in 24 British towns. PARTICIPANTS: Men aged 60–79 without prevalent HF followed for 9 years (N = 3,723). MEASUREMENTS: Information on incident HF cases was obtained from primary care records. Assessment of sleep was based on self‐reported sleep duration at night and daytime napping. RESULTS: Self‐reported short nighttime sleep duration and daytime sleep of longer than 1 hour were associated with preexisting CVD, breathlessness, depression, poor health, physical inactivity, and manual social class. In all men, self‐reported daytime sleep of longer than 1 hour duration was associated with significantly greater risk of HF after adjustment for potential confounders (adjusted hazard ratio (aHR) = 1.69, 95% CI = 1.06–2.71) than in those who reported no daytime napping. Self‐reported nighttime sleep duration was not associated with HF risk except in men with preexisting CVD (<6 hours: aHR = 2.91, 95% CI = 1.31–6.45; 6 hours: aHR = 1.89, 95% CI = 0.89–4.03; 8 hours: aHR = 1.29, 95% CI = 0.61–2.71; ≥9 hours: aHR = 1.80, 905% CI = 0.71–4.61 vs nighttime sleep of 7 hours). Snoring was not associated with HF risk. CONCLUSION: Self‐reported daytime napping of longer than 1 hour is associated with greater risk of HF in older men. Self‐reported short sleep (<6 hours) in men with CVD is associated with particularly high risk of developing HF.
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spelling pubmed-50312112016-10-03 Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study Wannamethee, S. Goya Papacosta, Olia Lennon, Lucy Whincup, Peter H. J Am Geriatr Soc Brief Reports OBJECTIVES: To examine the associations between self‐reported nighttime sleep duration and daytime sleep and incident heart failure (HF) in men with and without preexisting cardiovascular disease (CVD). DESIGN: Population‐based prospective study. SETTING: General practices in 24 British towns. PARTICIPANTS: Men aged 60–79 without prevalent HF followed for 9 years (N = 3,723). MEASUREMENTS: Information on incident HF cases was obtained from primary care records. Assessment of sleep was based on self‐reported sleep duration at night and daytime napping. RESULTS: Self‐reported short nighttime sleep duration and daytime sleep of longer than 1 hour were associated with preexisting CVD, breathlessness, depression, poor health, physical inactivity, and manual social class. In all men, self‐reported daytime sleep of longer than 1 hour duration was associated with significantly greater risk of HF after adjustment for potential confounders (adjusted hazard ratio (aHR) = 1.69, 95% CI = 1.06–2.71) than in those who reported no daytime napping. Self‐reported nighttime sleep duration was not associated with HF risk except in men with preexisting CVD (<6 hours: aHR = 2.91, 95% CI = 1.31–6.45; 6 hours: aHR = 1.89, 95% CI = 0.89–4.03; 8 hours: aHR = 1.29, 95% CI = 0.61–2.71; ≥9 hours: aHR = 1.80, 905% CI = 0.71–4.61 vs nighttime sleep of 7 hours). Snoring was not associated with HF risk. CONCLUSION: Self‐reported daytime napping of longer than 1 hour is associated with greater risk of HF in older men. Self‐reported short sleep (<6 hours) in men with CVD is associated with particularly high risk of developing HF. John Wiley and Sons Inc. 2016-06-28 2016-09 /pmc/articles/PMC5031211/ /pubmed/27351127 http://dx.doi.org/10.1111/jgs.14255 Text en © 2016 The Authors. The Journal of the American Geriatrics Society published by Wiley Periodicals, Inc. on behalf of The American Geriatrics Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Reports
Wannamethee, S. Goya
Papacosta, Olia
Lennon, Lucy
Whincup, Peter H.
Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study
title Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study
title_full Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study
title_fullStr Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study
title_full_unstemmed Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study
title_short Self‐Reported Sleep Duration, Napping, and Incident Heart Failure: Prospective Associations in the British Regional Heart Study
title_sort self‐reported sleep duration, napping, and incident heart failure: prospective associations in the british regional heart study
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031211/
https://www.ncbi.nlm.nih.gov/pubmed/27351127
http://dx.doi.org/10.1111/jgs.14255
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