Impact of Acute Exercise on Vascular Insulin Sensitivity in Metabolic Syndrome
1 other identifier
interventional
16
1 country
1
Brief Summary
Obesity is an independent risk factor for type 2 diabetes and cardiovascular disease. The increased prevalence of obesity worldwide is a major concern among the scientific and medical communities. Insulin resistance is a common factor associated with obesity, metabolic syndrome, hypertension, and type 2 diabetes. Individuals affected by these conditions often experience endothelial dysfunction as well. Insulin resistance provides a key link between metabolic syndrome risk factors and vascular disease. Development of strategies aimed at preventing vascular dysfunction and future disease caused by metabolic disturbances is needed. Although the relationship between obesity and various diseases is well known, the acute effects of insulin on vascular function in obese individuals have yet to be fully determined. Additionally, the effects of acute exercise on insulin-stimulated endothelial function are unknown. Exercise may be an effective and potent treatment that protects against endothelial dysfunction, insulin resistance, and future cardiometabolic disease commonly present with obesity. However, less attention has been placed on vascular insulin sensitivity. The purpose of this study is to test the hypothesis that a single bout of exercise increases insulin-stimulated blood flow at the macro- and micro-vasculature level in obese individuals with metabolic syndrome to similar levels as healthy obese control. Our laboratory has available non-invasive methods to quantify vascular function and the gold-standard technique for assessing insulin sensitivity (euglycemic-hyperinsulinemic clamp). The investigators will assess vascular function (flow-mediated dilation, post-ischemic flow velocity and contrast-enhanced ultrasound) as well as arterial stiffness (augmentation index and pulse wave velocity) before and at the end of the clamp protocol performed the morning following a bout of exercise and a control (no-exercise) condition in 1) metabolic syndrome and 2) obese adults. If our hypothesis is sustained, it will suggest that a key role of the vasculature exists in regulating insulin following exercise and will provide insight into the link between the vasculature, obesity, metabolic syndrome and cardiovascular disease and may confer decreased risk for cardiometabolic disease.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2019
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 18, 2019
CompletedFirst Submitted
Initial submission to the registry
March 5, 2019
CompletedFirst Posted
Study publicly available on registry
March 28, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2020
CompletedMarch 28, 2019
March 1, 2019
7 months
March 5, 2019
March 26, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Effect of single bout of exercise on FMD
Flow Mediated Dilation (FMD) as a percentage
Baseline clamp study
Effect of single bout of exercise on CEU
Contrast Enhanced Ultrasound (CEU) as a percentage
Baseline Clamp Study
Comparison of insulin stimulated FMD response
Flow mediated dilation as a percentage of fasting values
Through study completion, up to about 4 weeks
Comparison of insulin stimulated CEU response
Contrast Enhanced Ultrasound (CEU) as a percentage of fasting values
Through study completion, up to about 4 weeks
Secondary Outcomes (7)
Systemic Arterial stiffness
Through study completion, up to about 4 weeks
Central Arterial Stiffness
Through study completion, up to about 4 weeks
Metabolic Flexibility
Through study completion, up to about 4 weeks
Fasting glucose
Through study completion, up to about 4 weeks
Fasting insulin
Through study completion, up to about 4 weeks
- +2 more secondary outcomes
Study Arms (2)
Control
ACTIVE COMPARATORSubjects with simple obesity will complete 2 different testing conditions in a counterbalanced order with at least one week between conditions. 10-12 hrs post test condition the subject will report for a Euglycemic-Hyperinsulinemic clamp study, where Flow Mediated Dilation (FMD) and Contrast Enhanced Ultrasound (CEU) will be performed.
Metabolic Syndrome
ACTIVE COMPARATORSubjects with metabolic syndrome will complete 2 different testing conditions in a counterbalanced order with at least one week between conditions. 10-12 hrs post test condition the subject will report for a Euglycemic-Hyperinsulinemic clamp study, where Flow Mediated Dilation (FMD) and Contrast Enhanced Ultrasound (CEU) will be performed.
Interventions
An exercise condition, which will be walking at a moderate intensity (\~70% VO2peak). Time will vary based upon individual fitness levels to burn \~400kcals (estimated 0.5 - 1hr). Oxygen consumption will be measured during exercise via a metabolic cart to confirm energy expenditure. Participants will then rest following the exercise procedure for 20 minutes. Between 20 and 45 minutes following exercise, oxygen consumption will be measured to understand and capture excess post-exercise oxygen consumption (EPOC). Following this, participants will be provided with a standardize dinner and snack to consume in the AMP lab.
A control (no-exercise) condition. Participants will report to the AMP lab to rest for the same duration as the exercise bout and consume the standardized dinner and snack.
Eligibility Criteria
You may qualify if:
- Males and females, ages 40-70 years
- Never diagnosed with type 2 diabetes and/or cardiovascular disease
- Not currently engaged in \> 60 min/wk of exercise
- Healthy Obese: (BMI ≥ 30 kg/m2 but ≤ 45 kg/m2) and no other metabolic syndrome risk factors, excluding waist circumference.
- Metabolic Syndrome: (BMI ≥ 30 kg/m2 but ≤ 45 kg/m2) and must meet at least 3 out of 5 National Cholesterol Education Adult Treatment Panel III Metabolic Syndrome Criteria:
- Increased waist circumference (≥102 cm in men; ≥88 cm in women) Elevated triglycerides (≥150 mg/dl) or currently taking medication (Rx) Reduced HDL-cholesterol (\<40mg/dl in men, \<50 mg/dl in women) or currently taking medication (Rx) High blood pressure (≥130 mmHg systolic or ≥85mmHg diastolic) or currently taking medication (Rx) Elevated fasting glucose (≥100 mg/dl)
- Subject may participate if on the following drugs:
- Diuretics, ace-inhibitors and ARBs for treatment of hypertension
- Statins
You may not qualify if:
- Morbidly obese patients (BMI \>45 kg/m2) and overweight/lean patients (BMI \<30 kg/m2).
- Subjects who have not been weight stable (\>2kg weight change in past 3 months).
- Currently participating in a regular exercise training program ( \>30 min. of physical activity per day, \>2 days/week)
- Medication or food supplement that is known to affect insulin sensitivity or endothelial function (TZDs, sulfonylureas, biguanides, alpha-glucosidase inhibitors, phosphodiesterase inhibitors, beta-blockers, alpha-blockers, fibrates, glucocorticoids, fish oil, allopurinol)
- Subjects with abnormal estimated glomerular filtration rate (eGFR).
- Hypertriglyceridemic (\>400 mg/dl) subjects.
- Hypertensive (\>160/100 mmHg)
- Subjects taking vasoactive medications also known to affect heart rate and rhythm (i.e. Ca++ channel blockers, nitrates, alpha- or beta-blockers).
- Subjects with a history of significant metabolic, cardiac, congestive heart failure, cerebrovascular, hematological, pulmonary, gastrointestinal, liver, renal, or endocrine disease or cancer that in the investigator's opinion would interfere with or alter the outcome measures, or impact subject safety.
- Smoking presently or in the past 1 year.
- HbA1c ≥ 6.5
- Subjects currently taking Metformin or any active weight suppression medication (e.g. phentermine, orlistat, lorcaserin, naltrexone-bupropion in combination, liraglutide, benzphetamine, diethylpropion, phendimetrazine)
- Pregnant (as evidenced by positive pregnancy test) or breastfeeding
- Subjects with contraindications to participation in an exercise program
- Known hypersensitivity to perflutren (contained in Definity)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Virginialead
- American College of Sports Medicinecollaborator
Study Sites (1)
University of Virginia
Charlottesville, Virginia, 22904, United States
Related Publications (27)
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PMID: 23757424BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Steve Malin, PhD
University of Virginia
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assitant Professor
Study Record Dates
First Submitted
March 5, 2019
First Posted
March 28, 2019
Study Start
February 18, 2019
Primary Completion
September 30, 2019
Study Completion
January 31, 2020
Last Updated
March 28, 2019
Record last verified: 2019-03
Data Sharing
- IPD Sharing
- Will not share