Sleep disruptions and bone health: what do we know so far?


Journal

Current opinion in endocrinology, diabetes, and obesity
ISSN: 1752-2978
Titre abrégé: Curr Opin Endocrinol Diabetes Obes
Pays: England
ID NLM: 101308636

Informations de publication

Date de publication:
01 08 2021
Historique:
pubmed: 10 5 2021
medline: 16 10 2021
entrez: 9 5 2021
Statut: ppublish

Résumé

This review briefly summarizes the growing body of literature addressing the skeletal consequences of sleep and circadian disruption. The most recent data in the field suggest that the diurnal variation in bone turnover markers are because of endogenous circadian rhythmicity linked to clock genes in all bone cells; in a small human intervention study, cumulative sleep restriction with concurrent circadian disruption negatively alter bone turnover markers in a way that could explain the lower BMD and increased fracture risk identified in some prior night shift work studies; abnormal sleep duration and obstructive sleep apnea are associated with low BMD and increased fracture risk in some but not all studies. Normal physiology and some animal and human intervention studies suggest that sleep and circadian disruptions, such as night shift work, abnormal sleep durations and obstructive sleep apnea are detrimental to skeletal health. However, additional research in this area is needed to determine which sleep/circadian disturbances are most detrimental to skeletal health, the reversibility of such impairments, and underlying mechanisms.

Identifiants

pubmed: 33965968
doi: 10.1097/MED.0000000000000639
pii: 01266029-202108000-00004
pmc: PMC8244577
mid: NIHMS1698728
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

348-353

Subventions

Organisme : NIAMS NIH HHS
ID : L30 AR070515
Pays : United States
Organisme : NIAMS NIH HHS
ID : K23 AR070275
Pays : United States
Organisme : NIAMS NIH HHS
ID : R03 AR074509
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL151332
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK048520
Pays : United States

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

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Auteurs

Christine M Swanson (CM)

Division of Endocrinology, Metabolism and Diabetes, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.

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Classifications MeSH