Body Weight, Sleep, and Heart Health

Sponsor
Oregon Health and Science University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03388788
Collaborator
(none)
28
1
2
61
0.5

Study Details

Study Description

Brief Summary

A multidisciplinary investigation examining the circadian mechanisms regulating cardiovascular (CV) risk in obesity. Specifically, in a valid circadian protocol, the investigators aim to study resting cardiovascular risk markers and the reactivity of circadian rhythms in these risk markers to standardized stressors in obesity. Furthermore, using an ingenious approach, the investigators propose to explore impairment in pre/post synaptic function in the cardiac left ventricle.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

Overall, these studies will help us answer whether CV rhythms predispose obese individuals to increased CV disease risk - particularly around the vulnerable morning period. The results will serve as a foundation for clinical trials of appropriately timed dosing of medications targeting aspects of the CV system in obesity that increase effectiveness while decreasing side-effects.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
28 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Circadian Mechanisms of Cardiovascular Risk in Obesity
Actual Study Start Date :
May 1, 2018
Anticipated Primary Completion Date :
May 31, 2023
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Normal Weight

Healthy lean controls [18.5<BMI<25 kg/m2 and WC <94/80 (men and women respectively)] will participate in a 5-day circadian study protocol with PET imaging using radiopharmaceuticals (11C-meta-hydroxyephedrine, 11C-CGP12177, and O15-water).

Radiation: PET Imaging
Positron Emission Tomography (PET) imaging for research.

Behavioral: Circadian Study Protocol
5-day circadian study schedule

Drug: 11C-Meta-Hydroxyephedrine (mHED)
11C-meta-hydroxyephedrine will be used during PET imaging to measure cardiac presynaptic norepinephrine transporter function.
Other Names:
  • 11C-mHED
  • Drug: 11C-CGP12177
    Cardiac beta adrenergic receptor density will be measured via PET imaging with infusion of 11C-CGP12177.

    Drug: O15-water
    Blood flow will be measured via PET imaging with infusion of O15-water.

    Experimental: Overweight

    Healthy obese [30≤BMI<40 and waist circumference (WC) ≥94/80 (men and women respectively)] will participate in a 5-day circadian study protocol with PET imaging using radiopharmaceuticals (11C-meta-hydroxyephedrine, 11C-CGP12177, and O15-water).

    Radiation: PET Imaging
    Positron Emission Tomography (PET) imaging for research.

    Behavioral: Circadian Study Protocol
    5-day circadian study schedule

    Drug: 11C-Meta-Hydroxyephedrine (mHED)
    11C-meta-hydroxyephedrine will be used during PET imaging to measure cardiac presynaptic norepinephrine transporter function.
    Other Names:
  • 11C-mHED
  • Drug: 11C-CGP12177
    Cardiac beta adrenergic receptor density will be measured via PET imaging with infusion of 11C-CGP12177.

    Drug: O15-water
    Blood flow will be measured via PET imaging with infusion of O15-water.

    Outcome Measures

    Primary Outcome Measures

    1. Blood Pressure [5 Days]

      Beat-by-beat and ambulatory blood pressure measurements.

    Secondary Outcome Measures

    1. Heart Rate [5 Days]

      Heart rate via 2-channel echocardiogram (ECG)

    2. Epinephrine [5 days]

      Venous Epinephrine to estimate sympathetic output

    3. Norepinephrine [5 days]

      Venous Norepinephrine to estimate sympathetic output

    4. Cortisol [5 days]

      Saliva cortisol to estimate sympathetic output

    5. Aldosterone [5 days]

      Venous Aldosterone to estimate sympathetic output

    6. Endocannabinoid [5 days]

      Plasma endocannabinoid to estimate sympathetic regulation

    7. Heart Rate Variability (HRV) [5 days]

      Analysis of HRV from 12-lead ECG to assess parasympathetic activity

    8. malondialdehyde (MDA) adducts [5 days]

      Plasma MDA to measure oxidative stress and inflammation.

    9. Flow Mediated Dilation (FMD) [5 days]

      FMD to measure endothelial function.

    10. Tumor Necrosis Factor alpha (TNF-alpha) [5 days]

      TNF-alpha to assess inflammation.

    11. Coronary blood flow [5 days.]

      Radiolabeled water (O15-water) to measure coronary blood flow during PET Imaging.

    12. Norepinephrine reuptake transport [5 days.]

      Radiolabeled meta-hydroxyephedrine (11C-mHED) to measure norepinephrine reuptake during PET Imaging.

    13. Beta-adrenergic receptor density [5 days.]

      Radiolabeled agonist (11C-CGP12177) to measure beta-adrenergic receptors during PET Imaging.

    14. Dual Emission X-ray Absorbance (DEXA) Body composition [1 day]

      DEXA imaging to assess body composition.

    15. Coronary Artery Calcium Score [1 scan.]

      Coronary Calcium Computed Tomography (CT) Scan

    16. Coronary Microvascular Blood Flux [3 days]

      1. Determine in lean healthy humans if coronary microvascular function, measured as coronary microvascular blood flux, has an endogenous circadian rhythm with lowest function in the morning. 2. Test the hypothesis that people with obesity have impaired coronary microvascular blood flux compared to lean individuals, with the exaggerated impairment during the morning. Measured using myocardial contrast echocardiography.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Ages 25-65

    • Lean and overweight (BMI 18.5-40kg/m2)

    • Habitually sedentary

    Exclusion Criteria:
    • History of smoking/tobacco use

    • Insomnia

    • Moderate to severe obstructive sleep apnea.

    • Prior shift work within 6 months prior to the study.

    • Prescription medications

    • Drugs of abuse

    • Acute, chronic, or debilitating medical condition (including diabetes, hypertension, and metabolic syndrome)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Oregon Health & Science University Portland Oregon United States 97239

    Sponsors and Collaborators

    • Oregon Health and Science University

    Investigators

    • Principal Investigator: Steven A Shea, PhD, Oregon Institute of Occupational Health Sciences
    • Principal Investigator: Jeanne M Link, PhD, OHSU Center for Radiochemistry Research

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Steven A. Shea, Director, Oregon Health and Science University
    ClinicalTrials.gov Identifier:
    NCT03388788
    Other Study ID Numbers:
    • IRB00017489
    First Posted:
    Jan 3, 2018
    Last Update Posted:
    Feb 7, 2022
    Last Verified:
    Feb 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 7, 2022