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Article: The effect of sleep duration on hemoglobin and hematocrit: observational and Mendelian randomization study

TitleThe effect of sleep duration on hemoglobin and hematocrit: observational and Mendelian randomization study
Authors
Keywordssleep duration
hemoglobin
hematocrit
Mendelian randomization
Issue Date2020
PublisherOxford University Press. The Journal's web site is located at http://www.journalsleep.org
Citation
Sleep, 2020, v. 43 n. 7, article no. zsz325 How to Cite?
AbstractStudy Objective: Observationally sleep duration is positively associated with hemoglobin (Hgb), whether this association is causal and consistent by sex remains unclear. Here, we assessed the association of sleep duration with Hgb and hematocrit (Hct) observationally in late adolescence in a population-representative Chinese birth cohort “Children of 1997” with validation using Mendelian randomization (MR) in adults. Methods: In the “Children of 1997” birth cohort (recruited = 8327, included = 3144), we used multivariable linear regression to assess the adjusted associations of sleep duration (measured as time in bed) with Hgb and Hct at 17.5 years and any sex differences. Using two-sample MR, we assessed the effect of sleep duration on Hgb and Hct, based on 61 single nucleotide polymorphisms (SNPs) applied to genome-wide association studies of Hgb and Hct in adults (n = 361 194). Results: Observationally, self-reported sleep duration was positively associated with Hct (0.034 standard deviations [SDs] per hour, 95% confidence interval [CI] 0.019 to 0.049), but not with Hgb. Using MR longer sleep increased Hct (0.077 SD per hour, 95% CI 0.035 to 0.119) and Hgb (0.065 SD per hour, 95% CI 0.020 to 0.109) using Mendelian randomization pleiotropy residual sum and outlier (MR PRESSO), with more pronounced associations in men. Conclusions: Our novel findings indicate sleep increases both Hgb and Hct, particularly in men, perhaps contributing to its restorative qualities. Potential difference by sex and the implications of these findings warrant investigation.
Persistent Identifierhttp://hdl.handle.net/10722/282471
ISSN
2021 Impact Factor: 6.313
2020 SCImago Journal Rankings: 2.222
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWANG, J-
dc.contributor.authorKwok, MK-
dc.contributor.authorAu Yeung, SL-
dc.contributor.authorLi, AM-
dc.contributor.authorLam, S-
dc.contributor.authorLeung, GM-
dc.contributor.authorSchooling, CM-
dc.date.accessioned2020-05-15T05:28:33Z-
dc.date.available2020-05-15T05:28:33Z-
dc.date.issued2020-
dc.identifier.citationSleep, 2020, v. 43 n. 7, article no. zsz325-
dc.identifier.issn0161-8105-
dc.identifier.urihttp://hdl.handle.net/10722/282471-
dc.description.abstractStudy Objective: Observationally sleep duration is positively associated with hemoglobin (Hgb), whether this association is causal and consistent by sex remains unclear. Here, we assessed the association of sleep duration with Hgb and hematocrit (Hct) observationally in late adolescence in a population-representative Chinese birth cohort “Children of 1997” with validation using Mendelian randomization (MR) in adults. Methods: In the “Children of 1997” birth cohort (recruited = 8327, included = 3144), we used multivariable linear regression to assess the adjusted associations of sleep duration (measured as time in bed) with Hgb and Hct at 17.5 years and any sex differences. Using two-sample MR, we assessed the effect of sleep duration on Hgb and Hct, based on 61 single nucleotide polymorphisms (SNPs) applied to genome-wide association studies of Hgb and Hct in adults (n = 361 194). Results: Observationally, self-reported sleep duration was positively associated with Hct (0.034 standard deviations [SDs] per hour, 95% confidence interval [CI] 0.019 to 0.049), but not with Hgb. Using MR longer sleep increased Hct (0.077 SD per hour, 95% CI 0.035 to 0.119) and Hgb (0.065 SD per hour, 95% CI 0.020 to 0.109) using Mendelian randomization pleiotropy residual sum and outlier (MR PRESSO), with more pronounced associations in men. Conclusions: Our novel findings indicate sleep increases both Hgb and Hct, particularly in men, perhaps contributing to its restorative qualities. Potential difference by sex and the implications of these findings warrant investigation.-
dc.languageeng-
dc.publisherOxford University Press. The Journal's web site is located at http://www.journalsleep.org-
dc.relation.ispartofSleep-
dc.rightsPre-print: Journal Title] ©: [year] [owner as specified on the article] Published by Oxford University Press [on behalf of xxxxxx]. All rights reserved. Pre-print (Once an article is published, preprint notice should be amended to): This is an electronic version of an article published in [include the complete citation information for the final version of the Article as published in the print edition of the Journal.] Post-print: This is a pre-copy-editing, author-produced PDF of an article accepted for publication in [insert journal title] following peer review. The definitive publisher-authenticated version [insert complete citation information here] is available online at: xxxxxxx [insert URL that the author will receive upon publication here].-
dc.subjectsleep duration-
dc.subjecthemoglobin-
dc.subjecthematocrit-
dc.subjectMendelian randomization-
dc.titleThe effect of sleep duration on hemoglobin and hematocrit: observational and Mendelian randomization study-
dc.typeArticle-
dc.identifier.emailKwok, MK: maggiek@hku.hk-
dc.identifier.emailAu Yeung, SL: ayslryan@hku.hk-
dc.identifier.emailLeung, GM: gmleung@hku.hk-
dc.identifier.emailSchooling, CM: cms1@hkucc.hku.hk-
dc.identifier.authorityKwok, MK=rp02051-
dc.identifier.authorityAu Yeung, SL=rp02224-
dc.identifier.authorityLeung, GM=rp00460-
dc.identifier.authoritySchooling, CM=rp00504-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1093/sleep/zsz325-
dc.identifier.pmid31956914-
dc.identifier.scopuseid_2-s2.0-85088201209-
dc.identifier.hkuros309900-
dc.identifier.volume43-
dc.identifier.issue7-
dc.identifier.spagearticle no. zsz325-
dc.identifier.epagearticle no. zsz325-
dc.identifier.isiWOS:000608145900024-
dc.publisher.placeUnited States-
dc.identifier.issnl0161-8105-

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