Sleep duration regularity, but not sleep duration, is associated with microvascular function in college students

Abstract Study Objectives Vascular dysfunction is a hypothesized mechanism linking poor sleep habits to an increased incidence of cardiovascular diseases (CVDs). However, the vascular profile associated with free-living sleep duration and sleep regularity has not been well elucidated, particularly i...

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Veröffentlicht in:Sleep (New York, N.Y.) N.Y.), 2021-02, Vol.44 (2), p.1, Article 175
Hauptverfasser: Hoopes, Elissa K, Berube, Felicia R, D’Agata, Michele N, Patterson, Freda, Farquhar, William B, Edwards, David G, Witman, Melissa A H
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container_start_page 1
container_title Sleep (New York, N.Y.)
container_volume 44
creator Hoopes, Elissa K
Berube, Felicia R
D’Agata, Michele N
Patterson, Freda
Farquhar, William B
Edwards, David G
Witman, Melissa A H
description Abstract Study Objectives Vascular dysfunction is a hypothesized mechanism linking poor sleep habits to an increased incidence of cardiovascular diseases (CVDs). However, the vascular profile associated with free-living sleep duration and sleep regularity has not been well elucidated, particularly in young adults. Thus, this study aimed to evaluate the associations between mean sleep duration, regularity in sleep duration, and peripheral vascular function in young adult college students. Methods Fifty-one healthy undergraduate students (20 ± 1 years) completed 14 days of 24-hour wrist actigraphy and subsequent vascular assessments. Macrovascular function was measured using brachial artery flow-mediated dilation (FMD) while microvascular function was measured via passive leg movement (PLM). Results Mean sleep duration was unrelated to FMD and PLM. Conversely, more irregular sleep duration (14-day sleep duration standard deviation [SD]) was unfavorably associated with all three measures of PLM-induced hyperemia (peak leg blood flow [LBF], p = 0.01; change in LBF from baseline to peak, p < 0.01; LBF area under the curve, p < 0.01), and remained significant in regression models which adjusted for sex, body mass index, blood pressure, physical activity, alcohol and caffeine consumption, and sleep duration (all p < 0.05). When using a median split to dichotomize “low” and “high” sleep duration SD groups, those demonstrating high variability in sleep duration exhibited ~45% lower PLM responses compared with those demonstrating low variability. Conclusions Irregular sleep duration is associated with poorer microvascular function as early as young adulthood. These findings support the growing body of evidence that irregular sleep patterns may be an independent and modifiable risk factor for CVD.
doi_str_mv 10.1093/sleep/zsaa175
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However, the vascular profile associated with free-living sleep duration and sleep regularity has not been well elucidated, particularly in young adults. Thus, this study aimed to evaluate the associations between mean sleep duration, regularity in sleep duration, and peripheral vascular function in young adult college students. Methods Fifty-one healthy undergraduate students (20 ± 1 years) completed 14 days of 24-hour wrist actigraphy and subsequent vascular assessments. Macrovascular function was measured using brachial artery flow-mediated dilation (FMD) while microvascular function was measured via passive leg movement (PLM). Results Mean sleep duration was unrelated to FMD and PLM. Conversely, more irregular sleep duration (14-day sleep duration standard deviation [SD]) was unfavorably associated with all three measures of PLM-induced hyperemia (peak leg blood flow [LBF], p = 0.01; change in LBF from baseline to peak, p &lt; 0.01; LBF area under the curve, p &lt; 0.01), and remained significant in regression models which adjusted for sex, body mass index, blood pressure, physical activity, alcohol and caffeine consumption, and sleep duration (all p &lt; 0.05). When using a median split to dichotomize “low” and “high” sleep duration SD groups, those demonstrating high variability in sleep duration exhibited ~45% lower PLM responses compared with those demonstrating low variability. Conclusions Irregular sleep duration is associated with poorer microvascular function as early as young adulthood. These findings support the growing body of evidence that irregular sleep patterns may be an independent and modifiable risk factor for CVD.</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsaa175</identifier><identifier>PMID: 32905591</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adult ; Cardiovascular diseases ; Clinical Neurology ; College students ; Exercise ; Humans ; Life Sciences &amp; Biomedicine ; Movement ; Neurosciences ; Neurosciences &amp; Neurology ; Regional Blood Flow ; Risk factors ; Science &amp; Technology ; Sleep ; Sleep, Health and Disease ; Students ; Type 2 diabetes ; Vasodilation ; Young Adult ; Young adults</subject><ispartof>Sleep (New York, N.Y.), 2021-02, Vol.44 (2), p.1, Article 175</ispartof><rights>Sleep Research Society 2020. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com. 2020</rights><rights>Sleep Research Society 2020. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com.</rights><rights>COPYRIGHT 2021 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>21</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000649380000017</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c515t-b08beff2ff159bfd413e05dac4298e2fed5032f9ffb1583b26dc340084cfb7963</citedby><cites>FETCH-LOGICAL-c515t-b08beff2ff159bfd413e05dac4298e2fed5032f9ffb1583b26dc340084cfb7963</cites><orcidid>0000-0001-6561-3092</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,1585,27929,27930,39262,39263</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32905591$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoopes, Elissa K</creatorcontrib><creatorcontrib>Berube, Felicia R</creatorcontrib><creatorcontrib>D’Agata, Michele N</creatorcontrib><creatorcontrib>Patterson, Freda</creatorcontrib><creatorcontrib>Farquhar, William B</creatorcontrib><creatorcontrib>Edwards, David G</creatorcontrib><creatorcontrib>Witman, Melissa A H</creatorcontrib><title>Sleep duration regularity, but not sleep duration, is associated with microvascular function in college students</title><title>Sleep (New York, N.Y.)</title><addtitle>SLEEP</addtitle><addtitle>Sleep</addtitle><description>Abstract Study Objectives Vascular dysfunction is a hypothesized mechanism linking poor sleep habits to an increased incidence of cardiovascular diseases (CVDs). However, the vascular profile associated with free-living sleep duration and sleep regularity has not been well elucidated, particularly in young adults. Thus, this study aimed to evaluate the associations between mean sleep duration, regularity in sleep duration, and peripheral vascular function in young adult college students. Methods Fifty-one healthy undergraduate students (20 ± 1 years) completed 14 days of 24-hour wrist actigraphy and subsequent vascular assessments. Macrovascular function was measured using brachial artery flow-mediated dilation (FMD) while microvascular function was measured via passive leg movement (PLM). Results Mean sleep duration was unrelated to FMD and PLM. Conversely, more irregular sleep duration (14-day sleep duration standard deviation [SD]) was unfavorably associated with all three measures of PLM-induced hyperemia (peak leg blood flow [LBF], p = 0.01; change in LBF from baseline to peak, p &lt; 0.01; LBF area under the curve, p &lt; 0.01), and remained significant in regression models which adjusted for sex, body mass index, blood pressure, physical activity, alcohol and caffeine consumption, and sleep duration (all p &lt; 0.05). When using a median split to dichotomize “low” and “high” sleep duration SD groups, those demonstrating high variability in sleep duration exhibited ~45% lower PLM responses compared with those demonstrating low variability. Conclusions Irregular sleep duration is associated with poorer microvascular function as early as young adulthood. 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However, the vascular profile associated with free-living sleep duration and sleep regularity has not been well elucidated, particularly in young adults. Thus, this study aimed to evaluate the associations between mean sleep duration, regularity in sleep duration, and peripheral vascular function in young adult college students. Methods Fifty-one healthy undergraduate students (20 ± 1 years) completed 14 days of 24-hour wrist actigraphy and subsequent vascular assessments. Macrovascular function was measured using brachial artery flow-mediated dilation (FMD) while microvascular function was measured via passive leg movement (PLM). Results Mean sleep duration was unrelated to FMD and PLM. Conversely, more irregular sleep duration (14-day sleep duration standard deviation [SD]) was unfavorably associated with all three measures of PLM-induced hyperemia (peak leg blood flow [LBF], p = 0.01; change in LBF from baseline to peak, p &lt; 0.01; LBF area under the curve, p &lt; 0.01), and remained significant in regression models which adjusted for sex, body mass index, blood pressure, physical activity, alcohol and caffeine consumption, and sleep duration (all p &lt; 0.05). When using a median split to dichotomize “low” and “high” sleep duration SD groups, those demonstrating high variability in sleep duration exhibited ~45% lower PLM responses compared with those demonstrating low variability. Conclusions Irregular sleep duration is associated with poorer microvascular function as early as young adulthood. These findings support the growing body of evidence that irregular sleep patterns may be an independent and modifiable risk factor for CVD.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>32905591</pmid><doi>10.1093/sleep/zsaa175</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-6561-3092</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Cardiovascular diseases
Clinical Neurology
College students
Exercise
Humans
Life Sciences & Biomedicine
Movement
Neurosciences
Neurosciences & Neurology
Regional Blood Flow
Risk factors
Science & Technology
Sleep
Sleep, Health and Disease
Students
Type 2 diabetes
Vasodilation
Young Adult
Young adults
title Sleep duration regularity, but not sleep duration, is associated with microvascular function in college students
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