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Magnetic Resonance Imaging-Portfolio Diet Study #7 (MRIPD#7)

Primary Purpose

Cardiovascular Diseases, Hypercholesterolemia, Diabetes

Status
Withdrawn
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Portfolio Plus Diet
DASH-like (high fibre) dietary advice
Sponsored by
Unity Health Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiovascular Diseases focused on measuring Arterial plaque, portfolio diet, dietary modification, dietary trials, Canadian Network, knowledge synthesis and translation, Magnetic resonance imaging

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Eligible participants will be:

  1. Adult males that are within 30% of their target LDL-cholesterol for the low or moderate risk category according to the 2012 Canadian Cardiovascular Society Guidelines.
  2. Postmenopausal women that are within 30% of their target LDL-cholesterol for the low or moderate risk category according to the 2012 Canadian Cardiovascular Society Guidelines.

Participants will have the following characteristics:

  • BMI 25-40 kg/m2 with body weight that has remained constant (within ±2kg) over the last 3 months preceding the onset of the study.
  • Measurable arterial thickening at screening (carotid intima-media thickness of >1.0mm)
  • Plus at least 1 of the following 3 criteria:

    • are treated with statins
    • are statin intolerant
    • have refused statin treatment after consultation with the appropriate physician

Exclusion Criteria:

Individuals with the following conditions will be excluded:

  • major cardiovascular event

    • stroke or
    • myocardial infarction
  • Cardiac conditions that compromise normal function

    • mitral valve disease
    • heart failure
    • angina
  • familial hypercholesterolemia
  • secondary causes of hypercholesterolemia

    • hypothyroidism (unless treated and on a stable dose of L-thyroxine)
    • renal or liver disease
  • diabetes
  • serum triglycerides >4.5 mmol/L
  • uncontrolled blood pressure
  • major disability
  • disorders requiring continuous medical attention and treatment

    • chronic heart failure
    • liver disease
    • renal failure
    • cancer (except non-melanoma skin cancer--basal cell, squamous cell)
  • chronic infections (bacterial or viral)
  • chronic inflammatory diseases ( lupus, ulcerative colitis)
  • other autoimmune diseases (eg celiac disease or gluten sensitivity)
  • major surgery <6 months prior to randomization
  • conditions that make them unsuitable for MRI (e.g. have metal implants or are claustrophobic)
  • alcohol consumption >2 drinks/ day

Sites / Locations

  • Healthy Heart Lipid Clinic, St. Paul's Hospital
  • Richardson Center for Functional Foods and Nutraceuticals and the St. Boniface Hospital Cardiovascular Center, University of Manitoba
  • Risk Factor Modification Centre, St. Michael's Hospital
  • Institute of Nutraceuticals and Functional Foods and the Quebec Heart and Lung Institute, Laval University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Portfolio Plus Diet

DASH-like (high fibre) diet

Arm Description

Participants will be advised to follow a low glycemic index dietary portfolio. Specifically, the advice will be to limit saturated fat (to <7% of total calories and cholesterol to <200 mg/d) plus inclusion of viscous fibres, soy protein, plant sterols and nuts, 5% extra monounsaturated fat and selection of low glycemic index foods; emphasizing current recommendations for fruit and vegetable intakes (5-10 servings/d)

The DASH-like dietary advice will emphasize a diet of whole grains, low-fat dairy and current recommendations for fruit and vegetables (5-10 servings/day)

Outcomes

Primary Outcome Measures

Change from baseline of the maximum vessel wall volume of the carotid arteries
Assessed by MRI

Secondary Outcome Measures

Intra-plaque hemorrhage (IPH)
Assessed by MRI
Intra-plaque lipid (lipid-rich necrotic core)
Assessed by MRI
blood pressure and pulse rate
initiation of statin therapy
According to current CCS guidelines

Full Information

First Posted
February 18, 2014
Last Updated
April 25, 2017
Sponsor
Unity Health Toronto
Collaborators
Canadian Institutes of Health Research (CIHR), University of Toronto, Laval University, University of Manitoba, University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT02078635
Brief Title
Magnetic Resonance Imaging-Portfolio Diet Study #7
Acronym
MRIPD#7
Official Title
The Canada-wide Human Nutrition Trialists' Network
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Withdrawn
Why Stopped
Study was amalgamated with another study to include exercise as another intervention.
Study Start Date
undefined (undefined)
Primary Completion Date
October 7, 2014 (Actual)
Study Completion Date
October 7, 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Unity Health Toronto
Collaborators
Canadian Institutes of Health Research (CIHR), University of Toronto, Laval University, University of Manitoba, University of British Columbia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Presently in Canada, 29% of deaths are due to cardiovascular disease (CVD), costing $20.9 billion annually. The investigators have, therefore, brought together an unique network of investigators at different stages in their careers with a range of disciplines (nutrition, cardiology, diabetes, imaging, physics, clinical trials, statistics, laboratory medicine, primary care, genetics, psychology, knowledge translation (KT), and epidemiology) and with international recognition , experience and connections, to undertake a multi-centre study which will test the ability of the dietary Portfolio PLUS approach over 3 years to reduce the progression of plaque build-up in the carotid artery as assessed by Magnetic Resonance Imaging (MRI) in individuals with hypercholesterolemia. The dietary portfolio of cholesterol-lowering foods (viscous fibres, soy protein, plant sterol and nuts) which has been proven in many of their studies to be an effective cholesterol-lowering diet will be further enhanced by increased levels of monounsaturated fats (MUFA) and low glycemic index foods. Will this enhanced dietary strategy (dietary Portfolio PLUS ) reduce the progression of carotid atheromatous lesions, LDL-C and blood pressure while reducing the number of hyperlipidemic individuals requiring statins?
Detailed Description
As Western populations age and as body weight increases, the need for dietary strategies to reduce Coronary Heart Disease (CHD) risk continues. The investigators are now in a position to put together a dietary approach which will be a significant advance over current dietary advice for CHD risk reduction. The investigators believe this study using imaging and functional techniques is now needed to 1) demonstrate an improvement in estimated CHD risk based on anatomical changes rather than serum risk factors. 2) encourage popular uptake and clinical use of this combination dietary strategy and 3) stimulate a larger longer term trial with CHD events. Participants for this study will be recruited in 4 academic centres across Canada (Quebec, Toronto, Winnipeg and Vancouver). They will be in the low or moderate risk category based on the current Canadian Cardiovascular Society's (CCS) Guidelines 2012 and would normally be considered for initial treatment with lifestyle only. All participants will first be screened by ultrasound for the presence of plaque in the carotid arteries and will then be randomized to one of the 2 treatment arms: Portfolio Plus diet (test) or modified DASH diet (control), both given as routine clinical advice with follow up visits at 3-month intervals for 6 months and then twice yearly for the remainder of the 3 year trial. Prior to starting either diet, participants will undergo screening ultrasound examination of both right and left carotids to enable selection of those individuals whose intima-media thickness would be 5-30% below the cut point considered by the Mannheim Consensus as relevant arterial thickening to ensure a relatively low risk group, yet with some measurable arterial thickening. The main outcome will be MRI assessment of maximum vessel wall volume. This assessment will be repeated at year 3. It will be emphasized at the outset that both the dietary portfolio and the DASH-like diets have been associated with benefits in terms of cholesterol reduction to provide equal encouragement for those randomized to the test and control groups. Portfolio and DASH-like dietary advice will consist of half hour individual sessions with the dietitian at baseline, 3, and 6 months and then at 6-month intervals. Prior to starting each diet, instruction will be given on achieving the dietary goals. At follow-up visits, the participants' completed 7-day diet records will be discussed and the original advice reinforced. Every effort will be made to obtain study blood samples and carotid imaging data from all subjects at the designated times regardless of adherence to the dietary aspects of the study protocol. All subjects will be included in the intention-to-treat analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Hypercholesterolemia, Diabetes, Metabolic Syndrome, Obesity
Keywords
Arterial plaque, portfolio diet, dietary modification, dietary trials, Canadian Network, knowledge synthesis and translation, Magnetic resonance imaging

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Portfolio Plus Diet
Arm Type
Experimental
Arm Description
Participants will be advised to follow a low glycemic index dietary portfolio. Specifically, the advice will be to limit saturated fat (to <7% of total calories and cholesterol to <200 mg/d) plus inclusion of viscous fibres, soy protein, plant sterols and nuts, 5% extra monounsaturated fat and selection of low glycemic index foods; emphasizing current recommendations for fruit and vegetable intakes (5-10 servings/d)
Arm Title
DASH-like (high fibre) diet
Arm Type
Active Comparator
Arm Description
The DASH-like dietary advice will emphasize a diet of whole grains, low-fat dairy and current recommendations for fruit and vegetables (5-10 servings/day)
Intervention Type
Behavioral
Intervention Name(s)
Portfolio Plus Diet
Other Intervention Name(s)
Dietary Portfolio of cholesterol-lowering foods, Enhanced portfolio, Portfolio eating plan
Intervention Description
Foods on the Portfolio Plus plan will contribute 9 g/1000 kcal viscous fibre as β-glucan (oats, barley, oat bran bread and soups) and psyllium (cereal), 1 g plant sterol/1000 kcal diet (in sterol margarine), 22.5 g soy protein/1000 kcal (soy burgers, dogs, links, other soy meat analogues, soy milks, yogurts and cheese) and additional sources of plant proteins from pulses (eg. lentils, chickpeas, beans, etc); and 22.5 g almonds or equivalent of other nuts/1000 kcal and increase MUFA (as olive and canola oils, avocados, nuts, margarine and salad dressings). The glycemic index will be reduced from 83 to 70 GI units (bread scale)
Intervention Type
Behavioral
Intervention Name(s)
DASH-like (high fibre) dietary advice
Other Intervention Name(s)
high fibre diet
Intervention Description
Dietary advice will be given to encourage intake of whole grain foods (brown rice, whole wheat breads, muffins and breakfast cereals); to reduce red meat consumption, choose low fat dairy foods and a control margarine
Primary Outcome Measure Information:
Title
Change from baseline of the maximum vessel wall volume of the carotid arteries
Description
Assessed by MRI
Time Frame
At baseline and year 3
Secondary Outcome Measure Information:
Title
Intra-plaque hemorrhage (IPH)
Description
Assessed by MRI
Time Frame
At baseline and year 3
Title
Intra-plaque lipid (lipid-rich necrotic core)
Description
Assessed by MRI
Time Frame
baseline and year 3
Title
blood pressure and pulse rate
Time Frame
At months 0, 3, 6, 12, 18, 24, 30, 36
Title
initiation of statin therapy
Description
According to current CCS guidelines
Time Frame
baseline and year 3
Other Pre-specified Outcome Measures:
Title
LDL-cholesterol
Time Frame
At months, 0, 3, 6, 12, 18, 24, 30, 36
Title
HDL-cholesterol
Time Frame
months 0, 3, 6, 12, 18, 24, 30, 36
Title
C-reactive protein (CRP)
Time Frame
At months 0, 12, 24, and 36
Title
The Medical Outcomes Study 36-Item Short Form Questionnaire (SF-36)
Description
Survey on quality of life.
Time Frame
Months 0 and 36
Title
Genetic whole genome testing
Description
One time sample collection of buffy coat white cells for future analysis
Time Frame
month 0
Title
satiety of the test and control diet
Description
Participants will assess their level of satiety on the test/control diet at each visit using a 9-point bipolar semantic scale ranging from -4 (being starved/ feeling weak and faint with hunger) to +4 (being Painfully full) with 0 being neutral (ie don't mind eating a little more or less).
Time Frame
Months 0, 3, 6, 12, 18, 24, 30, 36
Title
Palatability of the test / control diets
Description
The palatability of the diet will by measured using a numerical scale of 1 to 10 (1= strongly dislike and 10 = like very much).
Time Frame
Months 3, 6, 12, 18, 24, 30, and 36

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Eligible participants will be: Adult males that are within 30% of their target LDL-cholesterol for the low or moderate risk category according to the 2012 Canadian Cardiovascular Society Guidelines. Postmenopausal women that are within 30% of their target LDL-cholesterol for the low or moderate risk category according to the 2012 Canadian Cardiovascular Society Guidelines. Participants will have the following characteristics: BMI 25-40 kg/m2 with body weight that has remained constant (within ±2kg) over the last 3 months preceding the onset of the study. Measurable arterial thickening at screening (carotid intima-media thickness of >1.0mm) Plus at least 1 of the following 3 criteria: are treated with statins are statin intolerant have refused statin treatment after consultation with the appropriate physician Exclusion Criteria: Individuals with the following conditions will be excluded: major cardiovascular event stroke or myocardial infarction Cardiac conditions that compromise normal function mitral valve disease heart failure angina familial hypercholesterolemia secondary causes of hypercholesterolemia hypothyroidism (unless treated and on a stable dose of L-thyroxine) renal or liver disease diabetes serum triglycerides >4.5 mmol/L uncontrolled blood pressure major disability disorders requiring continuous medical attention and treatment chronic heart failure liver disease renal failure cancer (except non-melanoma skin cancer--basal cell, squamous cell) chronic infections (bacterial or viral) chronic inflammatory diseases ( lupus, ulcerative colitis) other autoimmune diseases (eg celiac disease or gluten sensitivity) major surgery <6 months prior to randomization conditions that make them unsuitable for MRI (e.g. have metal implants or are claustrophobic) alcohol consumption >2 drinks/ day
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David J Jenkins, MD
Organizational Affiliation
St. Michael's Hospital / University of Toronto
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Benoit Lamarche, PhD
Organizational Affiliation
Laval University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Peter Jones, PhD
Organizational Affiliation
University of Manitoba
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jiri Frohlich, MD
Organizational Affiliation
University of British Columbia
Official's Role
Study Director
Facility Information:
Facility Name
Healthy Heart Lipid Clinic, St. Paul's Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6Z 1Y6
Country
Canada
Facility Name
Richardson Center for Functional Foods and Nutraceuticals and the St. Boniface Hospital Cardiovascular Center, University of Manitoba
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3T 6C5
Country
Canada
Facility Name
Risk Factor Modification Centre, St. Michael's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5C 2T2
Country
Canada
Facility Name
Institute of Nutraceuticals and Functional Foods and the Quebec Heart and Lung Institute, Laval University
City
Quebec City
State/Province
Quebec
ZIP/Postal Code
G1V 4G2
Country
Canada

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Magnetic Resonance Imaging-Portfolio Diet Study #7

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