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Effects of Low and Moderate Fat Diets on Lipids, Inflammation and Vascular Reactivity in the Metabolic Syndrome

Primary Purpose

Metabolic Syndrome X, Dyslipidemias

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Moderate Fat and Moderate Carbohydrate Diet
Low Fat and High Carbohydrate Diet
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome X focused on measuring Obesity, Hypertension, Insulin Resistance

Eligibility Criteria

30 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Metabolic Syndrome: individuals must have at least three of the following five criteria: Abdominal obesity greater than 90 cm in Asian men, greater than 102 cm in all other men, greater than 80 cm in Asian women, and greater than 88 cm in all other women Triglycerides greater than or equal to 150 mg/dL at two screening visits (Required for the purposes of this study, which focuses on the dyslipidemic phenotype) HDL cholesterol levels less than 40 mg/dL in men and less than 50 mg/dL in women Blood pressure levels greater than 130/85 mmHg or taking an allowed blood pressure medication at Visit 1 (see definition in exclusions below) Fasting glucose greater than or equal to 100mg/dL at Visit 1 Exclusion Criteria: LDL greater than or equal to 190 mg/dL Triglycerides greater than 500mg/dL at Visit 1 Blood pressure over a mean of 150/95 at the two first visits Body mass index greater than 40 kg/m² Currently taking any lipid lowering medication other than statins Currently taking high doses of thiazide diuretics (greater than 50mg/day), or any other blood pressure medication in the past 4 weeks Use of plant sterols from sources such as Benecol or Take Control margarines in the past 4 weeks Use of any fish oil supplements in the week prior to screening Blood glucose greater than 140 mg/dL or use of diabetes medications Hospitalization for coronary disease in the last 6 months Use of nitroglycerin or other nitrates Unstable liver, renal, gastrointestinal or pulmonary disease or mental disease, or medically unstable for other reasons Alcohol intake greater than 2 drinks/day, any illegal drug use, smoking, chronic NSAID use or NSAID use within 5 days before the BAR study Pregnancy intended within one year or one year prior or currently lactating In reproductive age women, an irregular menstrual cycle (must have consistent menstrual cycle between 24 to 32 days) Use or expectation of use of oral or patch contraceptive Unable or unlikely to be able to comply with study requirements

Sites / Locations

  • Northwest Lipid Research Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Group 1

Group 2

Arm Description

Subjects consume study diets in the following order: Diet 1 (20% fat diet) for 1 month with all food provided, American Heart Association Step I Diet for 1 month at home, and Diet 2 (40% fat diet) for 1 month with all food provided and then continue to follow this diet for an additional 4 months at home.

Subjects consume study diets in the following order: Diet 2 (40% fat diet) for 1 month with all food provided, American Heart Association Step I Diet for 1 month at home, and Diet 1 (20% fat diet) for 1 month with all food provided and then continue to follow this diet for an additional 4 months at home.

Outcomes

Primary Outcome Measures

Non-HDL cholesterol
C-reactive protein
Brachial artery reactivity

Secondary Outcome Measures

Full Information

First Posted
August 10, 2006
Last Updated
October 27, 2010
Sponsor
University of Washington
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00362908
Brief Title
Effects of Low and Moderate Fat Diets on Lipids, Inflammation and Vascular Reactivity in the Metabolic Syndrome
Official Title
Diets for Dyslipidemia in the Metabolic Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
October 2010
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Washington
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The metabolic syndrome consists of five concurrent conditions which increase risk of heart disease, stroke, and diabetes. Persons with the metabolic syndrome usually have high triglyceride and low HDL levels and are overweight. Low fat, high carbohydrate diets may not provide the same cholesterol-lowering benefits to obese individuals as they do to non-obese individuals. The purpose of this study is to compare the effects of a low fat, high carbohydrate diet versus a moderate fat, moderate carbohydrate diet on the heart, blood vessels, and cholesterol levels in individuals with metabolic syndrome.
Detailed Description
The Metabolic Syndrome is characterized by elevated insulin levels, excess body fat in the waist, and elevated levels of glucose and blood pressure, and dyslipidemia. Dyslipidemia in the Metabolic Syndrome is characterized by high levels of triglycerides, low levels of HDL cholesterol, and above average LDL and non-HDL cholesterol. Individuals with elevated LDL cholesterol have traditionally been advised to follow a low fat, high carbohydrate diet. However, research has shown that this diet does not adequately regulate cholesterol levels in individuals with dyslipidemia. A diet consisting of more moderate amounts of fats and carbohydrates may be more beneficial for individuals with the dyslipidemia of the metabolic syndrome. The purpose of this study is to compare the effects of a diet moderate in fat and carbohydrate versus a low fat, high carbohydrate diet on the cholesterol levels, inflammatory factors and vascular response in individuals with metabolic syndrome. During the initial screening period, participants follow an American Heart Association (AHA) Step 1 diet and cholesterol levels are tested for eligibility under the criteria of the Metabolic Syndrome. Before being randomized, eligible participants have a frequently sampled intravenous glucose tolerance test (FSIVGTT), an abdominal CT scan to measure fat content in two locations and two brachial artery reactivity tests. The FSIVGTT provides information about whether participants are insulin sensitive or insulin resistant. The CT scan measures the fat content in the abdomen and the liver. The brachial artery reactivity tests measure blood flow through the brachial artery in the arm. This 7-month study consists of two 1-month feeding periods, a rest month between the two feeding periods and a 4-month follow-up diet in a free-living setting. In Month 1, participants are randomly assigned to follow either a moderate fat, moderate carbohydrate diet or a low fat, high carbohydrate diet. Participants receive prepared food at study visits twice a week. Weight and vital signs are measured at each study visit, and blood is collected at baseline, and Weeks 3-1/2 and 4. A brachial artery reactivity test, using an ultrasound to measure artery size and blood flow in the arm, is performed twice in Week 4. In the Month 2 rest period, participants follow an AHA Step 1 diet at home. In Month 3, participants switch to the other diet and all study procedures and evaluations are repeated as in Month 1. During the following Months 4 through 7, participants continue following the second assigned diet, but are responsible for preparing their own food. They meet with a dietician once a week for 1 month to learn how to prepare meals at home. During this 4-month period, blood collection, vital sign measurements, and review of medical history and diet continue at monthly visits. At the end of Month 7, participants again undergo two brachial artery reactivity tests. As of October, 2010, 148 were screened with 71 eligible to be randomized. Seven discontinued prior to completion and 64 completed the 7 month study. The intervention is complete and analyses are ongoing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome X, Dyslipidemias
Keywords
Obesity, Hypertension, Insulin Resistance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
71 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Active Comparator
Arm Description
Subjects consume study diets in the following order: Diet 1 (20% fat diet) for 1 month with all food provided, American Heart Association Step I Diet for 1 month at home, and Diet 2 (40% fat diet) for 1 month with all food provided and then continue to follow this diet for an additional 4 months at home.
Arm Title
Group 2
Arm Type
Active Comparator
Arm Description
Subjects consume study diets in the following order: Diet 2 (40% fat diet) for 1 month with all food provided, American Heart Association Step I Diet for 1 month at home, and Diet 1 (20% fat diet) for 1 month with all food provided and then continue to follow this diet for an additional 4 months at home.
Intervention Type
Behavioral
Intervention Name(s)
Moderate Fat and Moderate Carbohydrate Diet
Intervention Description
40% allowable fat diet (less than or equal to 7% saturated fat) consumed for 1 or 5 months
Intervention Type
Behavioral
Intervention Name(s)
Low Fat and High Carbohydrate Diet
Intervention Description
20% fat diet (less than or equal to 7% saturated fat) consumed for 1 or 5 months
Primary Outcome Measure Information:
Title
Non-HDL cholesterol
Time Frame
Measured at screening, baseline, at the beginning and end of the 1st and 2nd diet periods, and at the end of each month for four months during the diet extension
Title
C-reactive protein
Time Frame
Measured at the beginning and end of the 1st and 2nd diet periods and at the end of the four month diet extension
Title
Brachial artery reactivity
Time Frame
Two measurements are done at the beginning and end the 1st and 2nd diet periods and at the end of the four month diet extension

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Metabolic Syndrome: individuals must have at least three of the following five criteria: Abdominal obesity greater than 90 cm in Asian men, greater than 102 cm in all other men, greater than 80 cm in Asian women, and greater than 88 cm in all other women Triglycerides greater than or equal to 150 mg/dL at two screening visits (Required for the purposes of this study, which focuses on the dyslipidemic phenotype) HDL cholesterol levels less than 40 mg/dL in men and less than 50 mg/dL in women Blood pressure levels greater than 130/85 mmHg or taking an allowed blood pressure medication at Visit 1 (see definition in exclusions below) Fasting glucose greater than or equal to 100mg/dL at Visit 1 Exclusion Criteria: LDL greater than or equal to 190 mg/dL Triglycerides greater than 500mg/dL at Visit 1 Blood pressure over a mean of 150/95 at the two first visits Body mass index greater than 40 kg/m² Currently taking any lipid lowering medication other than statins Currently taking high doses of thiazide diuretics (greater than 50mg/day), or any other blood pressure medication in the past 4 weeks Use of plant sterols from sources such as Benecol or Take Control margarines in the past 4 weeks Use of any fish oil supplements in the week prior to screening Blood glucose greater than 140 mg/dL or use of diabetes medications Hospitalization for coronary disease in the last 6 months Use of nitroglycerin or other nitrates Unstable liver, renal, gastrointestinal or pulmonary disease or mental disease, or medically unstable for other reasons Alcohol intake greater than 2 drinks/day, any illegal drug use, smoking, chronic NSAID use or NSAID use within 5 days before the BAR study Pregnancy intended within one year or one year prior or currently lactating In reproductive age women, an irregular menstrual cycle (must have consistent menstrual cycle between 24 to 32 days) Use or expectation of use of oral or patch contraceptive Unable or unlikely to be able to comply with study requirements
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pathmaja Paramsothy, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwest Lipid Research Clinic
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17045076
Citation
Knopp RH, Fish B, Dowdy A, Retzlaff B, Walden C, Rusanu I, Paramsothy P. A moderate-fat diet for combined hyperlipidemia and metabolic syndrome. Curr Atheroscler Rep. 2006 Nov;8(6):492-500. doi: 10.1007/s11883-006-0025-9.
Results Reference
background
Citation
Paramsothy P, Krieger E, Chan E, Fish B, Dowdy A, Knopp RH. Abstract 1017: Moderate vs Low Fat Diet Effects on Lipids and Inflammation in Metabolic Syndrome. Circulation, Nov 2009; 120: S426. Presented as oral abstract at AHA Annual Scientific Session November, 2009.
Results Reference
result
Citation
Paramsothy P, Kreiger E, Chan E, Preus E, Rusanu I, Prager S, Knopp RH. Effects Of Low Fat Vs. Moderate Fat Diet On Insulin Resistance And Endothelial Function In Metabolic Syndrome. J. Am. Coll. Cardiol., March 9, 2010; 55: A58.E555. Presented as poster at ACC, Atlanta, GA. 3/10.
Results Reference
result

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Effects of Low and Moderate Fat Diets on Lipids, Inflammation and Vascular Reactivity in the Metabolic Syndrome

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