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Circadian Rhythm of Vascular Function in Midlife Adults
Saurabh S Thosar1, Alec M Berman1, Maya X Herzig1
1From the Oregon Institute of Occupational Health Sciences (S.S.T., A.M.B., M.X.H., A.W.M., N.P.B., N.A.C., M.P.B., J.S.E., S.A.S.), Oregon Health & Science University, Portland.
Insights
The body's internal clock (circadian system) impairs vascular endothelial function (VEF) and increases cardiovascular risk markers in the morning. This circadian rhythm contributes to the higher incidence of adverse cardiovascular events during morning hours.
Area of Science:
- Cardiovascular Physiology
- Chronobiology
- Endocrinology
Background:
- Adverse cardiovascular events disproportionately occur in the morning.
- Vascular endothelial function (VEF), a key cardiovascular risk marker, is impaired during this morning period.
- Previous research ruled out sleep or inactivity as causes for morning VEF impairment.
Purpose of the Study:
- To determine if the endogenous circadian system is responsible for morning VEF impairment.
- To assess the circadian system's effect on mechanistic biomarkers: oxidative stress (malondialdehyde adducts), endothelin-1, blood pressure, and heart rate.
Main Methods:
- Twenty-one healthy participants underwent a 5-day laboratory protocol with behaviors and measurements evenly distributed across 24 hours.
- Participants experienced recurring cycles of sleep and standardized waking episodes under dim light.
- Vascular endothelial function (VEF), blood pressure, heart rate, and blood biomarkers were measured during wake episodes.
Main Results:
- VEF was significantly attenuated during subjective night and morning hours, independent of behavior.
- Circadian rhythms were observed for malondialdehyde adducts and endothelin-1, peaking around noon.
- Systolic and diastolic blood pressure exhibited rhythmic patterns, peaking in the late afternoon.
Conclusions:
- The endogenous circadian system impairs VEF and elevates oxidative stress and endothelin-1 during morning hours.
- These circadian-driven changes may increase the risk of morning adverse cardiovascular events in susceptible individuals.
- This study highlights the critical role of the internal body clock in cardiovascular health vulnerabilities.
Abstract:
Objective- Adverse cardiovascular events occur more frequently in the morning than at other times of the day. Vascular endothelial function (VEF)-a robust cardiovascular risk marker-is impaired during this morning period. We recently discovered that this morning impairment in VEF is not caused by either overnight sleep or the inactivity that accompanies sleep. We determined whether the endogenous circadian system is responsible for this morning impairment in VEF. We also assessed whether the circadian system affects mechanistic biomarkers, that is, oxidative stress (malondialdehyde adducts), endothelin-1, blood pressure, and heart rate. Approach and Results- Twenty-one (11 women) middle-aged healthy participants completed a 5-day laboratory protocol in dim light where all behaviors, including sleep and activity, and all physiological measurements were evenly distributed across the 24-hour period. After baseline testing, participants underwent 10 recurring 5-hour 20-minute behavioral cycles of 2-hour 40-minute sleep opportunities and 2 hours and 40 minutes of standardized waking episodes. VEF, blood pressure, and heart rate were measured, and venous blood was sampled immediately after awakening during each wake episode. Independent of behaviors, VEF was significantly attenuated during the subjective night and across the morning ( P=0.04). Malondialdehyde adducts and endothelin-1 exhibited circadian rhythms with increases across the morning vulnerable period and peaks around noon ( P≤0.01). Both systolic ( P=0.005) and diastolic blood pressure ( P=0.04) were rhythmic with peaks in the late afternoon. Conclusions- The endogenous circadian system impairs VEF and increases malondialdehyde adducts and endothelin-1 in the morning vulnerable hours and may increase the risk of morning adverse cardiovascular events in susceptible individuals. Clinical Trial Registration- URL: http://www.clinicaltrials.gov . Unique identifier: NCT02202811.
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