Metabolic Syndrome Clinical Trial
— MUFA PUFAOfficial title:
Comparative Effects of Two Popular Diets in Veterans With the Metabolic Syndrome
Verified date | July 2014 |
Source | VA Office of Research and Development |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
The purpose of the study is to examine the effects of 2 commonly used diets, a Mediterranean
monounsaturated fatty acid enriched (MUFA) or AHA polyunsaturated (PUFA) enriched diet
combined with the VA Managing Overweight/Obesity for Veterans Everywhere (MOVE!) program so
as to determine which one is superior in reducing cardiometabolic risk factors associated
with Metabolic Syndrome. The risk factors considered include lipids and lipoproteins,
inflammatory markers such as CRP and adiponectin, endothelium-dependent flow-mediated
vasodilatation (FMD) and the postprandial lipid responses to a meal.
Cardiometabolic risk factors will be determined by measuring several cardiovascular risk
associated parameters including:
Biochemical measurements of lipids and inflammatory markers, body composition and VO2max
(Specific Objective 1, Descriptive).
Postprandial response to a meal challenge and endothelial vasoreactivity (FMD) assessed by
BART (Specific Objective 2, Physiological).
Determination of the effects on postheparin lipases and transfer protein activity, visceral
adipose tissue (VAT) and homeostasis model assessment-estimated insulin resistance (HOMA-IR)
(Specific Objective 3, Mechanistic)
Status | Completed |
Enrollment | 70 |
Est. completion date | April 2014 |
Est. primary completion date | April 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: Presence of 3 or more of the following): - Waist circumference >102 cm in men or >88 cm women - Treated Hypertension or Untreated Blood pressure >130/85 and < 160/100 mm Hg - Treated Hyperglycemia or Untreated Fasting blood glucose (FBG) >100 mg/dL (based on 2006 guidelines) - Treated Hyperlipidemia or Untreated Triglycerides > 150 mg/dL - HDL-C < 40 mg/dL men < 50 mg/dL women Exclusion Criteria: - Decompensated heart failure (NYHA Class IV); - Severe Pulmonary disease (Unable to walk on a treadmill at 2.5 mph or greater); - Chronic renal insufficiency (Cr > 2.5 mg/dL) - Treated diabetes mellitus with FBG > 180 mg/dL or HbA1C >9g % - Hematologic or malignant disorders - Treated SBP >160 mmHg and/or DBP > 95 mmHg ; - Treated TG > 250 mg/dL - Use of systemic vasodilators (e.g., nitrates) - Morbid Obesity (BMI > 50 kg/m2) - Endocrine (thyroid) or metabolic disorders (unless treated and under control) - Alcohol consumption greater than (2) 4-ounce glasses of table wine, (2) 12-oz bottles of beer or 2 shots of spirits in men or women - Active IV drug abuse within the past 6 months |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | VA Maryland Health Care System, Baltimore | Baltimore | Maryland |
Lead Sponsor | Collaborator |
---|---|
VA Office of Research and Development | University of Maryland |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Metabolic (lipid, glucose, insulin resistance), body composition (assessed via dual energy absorptiometry DXA and CT-scan), and CV fitness (assessed as maximal aerobic capacity, VO2max) abnormalities in Veterans with MetS. | 2 years | No | |
Secondary | Endothelium-dependent FMD assessed by the brachial artery reactivity test (BART) at rest and after postprandial meal challenge (lipid and glucose) responses. | 2 years | No | |
Secondary | (1) lipolytic enzymes and transfer proteins that mediate the lipid changes, (2) insulin resistance for glucose, (3) visceral adipose tissue area for lipids and glucose and (4) BART for vascular endothelial function and atherosclerosis. | 2 years | No |
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