Impact of Dairy Consumption on Inflammation: a Clinical Study (PLI) (PLI)
Primary Purpose
Cardiovascular Disease
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Dairy
Sponsored by

About this trial
This is an interventional prevention trial for Cardiovascular Disease focused on measuring Keywords;, Cardiovascular disease, Dairy, Inflammation, Blood lipids
Eligibility Criteria
Inclusion Criteria:
- Men and women aged between 18 and 70 years
- Presenting a subclinical inflammation (Plasma CRP >2 and <10 mg/l)
- Abdominal obesity, waist girth >94 cm in men and >80 cm in women
- Consumption of dairy products fewer than 2 servings per day
- Pre-menopausal women with regular menstrual cycle for the last 3 months
Exclusion Criteria:
- Plasma CRP <2 or >10 mg/l
- Smokers (>1 cigarette/day)
- Body weight variation >10% for the last 6 months prior to the study baseline
- BMI >35 kg/m2
- Previous history of CVD, type 2 diabetes and monogenic dyslipidemia
- Subjects taking medications for hyperlipidemia, hypertension
- Post menopausal women who have initiated hormone replacement therapy within 6 months of study onset
- Endocrine or gastrointestinal disorders
- Smoking
- Food allergies, milk aversion or intolerant to lactose
- Clinical use of vitamin D or calcium supplements
- Vegetarianism
Sites / Locations
- Institute of Nutraceutical and Functional Foods (INAF), Laval University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Dairy diet
Control diet
Arm Description
Outcomes
Primary Outcome Measures
Change in plasma CRP concentrations
Secondary Outcome Measures
Change in endothelial function
Change in plasma lipid concentrations (LDL-Cholesterol, HDL-C, triglycerides)
Change in insulin levels
Change in anthropometric measures (waist and hip circumferences)
Change in blood pressure
Change in CRP intravascular kinetics (in a subsample of the entire study population)
Full Information
NCT ID
NCT01444326
First Posted
September 28, 2011
Last Updated
April 1, 2014
Sponsor
Laval University
Collaborators
Dairy Farmers of Canada
1. Study Identification
Unique Protocol Identification Number
NCT01444326
Brief Title
Impact of Dairy Consumption on Inflammation: a Clinical Study (PLI)
Acronym
PLI
Official Title
Impact of Dairy Consumption on Inflammation: a Clinical Study
Study Type
Interventional
2. Study Status
Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
March 2010 (undefined)
Primary Completion Date
February 2012 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Laval University
Collaborators
Dairy Farmers of Canada
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Inflammation and endothelial dysfunction are being increasingly recognized as key etiological factors in the development of atherosclerosis and subsequent cardiovascular disease (CVD). These pro-atherogenic states are strongly correlated and often found co-segregating among individuals with obesity and the metabolic syndrome. There is increasing evidence to support the use in clinical practice of these novel markers of atherosclerosis and CVD risk. Recent data from the JUPITER study (Justification for the Use of Statins in Primary Prevention: An Intervention Trial Evaluating Rosuvastatin) has provided undisputable evidence that treating patients with elevated plasma CRP concentrations, a marker of systemic subclinical inflammation, leads to marked reduction in the risk of CHD even in patients with highly desirable LDL-C levels. There is also accumulating evidence associating endothelial dysfunction, which is defined as incapacity of the arteries to vasodilate when required, to an increased risk of CVD. While there are more and more studies on how diet affects inflammation and endothelial function, the impact of dairy consumption per se on these novel risk factors for CVD has not been well characterized.
The purpose of this study was to investigate the impact of dairy consumption on markers of inflammation and other risk factors in men and women with low grade systemic inflammation.
Detailed Description
This research will be undertaken as a multicenter randomized cross-over controlled study. A total of 140 men and women with subclinical inflammation (plasma CRP 2-10 mg/l) but otherwise healthy will consume two diets, one rich in dairy and one without dairy, while consuming a diet low in saturated fat (<10% energy), in trans fat (<1% energy) and in cholesterol (<200 mg/day). During the DAIRY diet, subjects will be asked to incorporate 3 servings of dairy (milk, yogurt, cheese) into their every day diet. During the CONTROL arm of the study, participants will be asked to consume energy equivalent replacement products. Each diet will be undertaken consecutively in random order and will have duration of approximately 28 days each (4 weeks).The primary analysis consists in comparing inflammation markers and related risk factors between the two treatments. The study is designed to detect a 12-16% difference in plasma CRP concentrations (the primary endpoint) between the control and the dairy diet.
A 2-week stabilization run-in period will precede the randomization of participants. During this run-in period, participants will be asked and instructed to adapt their diet to a prudent dietary pattern low in saturated fat (<10% energy), in trans fat (<1% energy) and in cholesterol (<200 mg/day). The total amount of fat in the diet will not be restricted, with recommendations ranging from 25-35% of energy. However, substitution of saturated for unsaturated fat will be advocated. Sodium intake <2300 mg/d will also be recommended. Recommendations will also include advice on how to restrict the consumption of processed and energy dense foods. The run-in diet will not include specific recommendation on dairy products. Participants will have the choice to include/exclude dairy from their prudent diet, as long as they comply with the main dietary recommendations. This 2-week run-in period will allow participants to familiarize themselves with the dietary recommendations used during the intervention per se. The two diets will be separated by a 4-week wash out period and will also consist to the prudent dietary pattern recommended. It must be stressed that foods will not be provided during the run-in and wash-out periods. These periods are imposed to minimize the inter- and intra-individual variability before and between the experimental phases.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Disease
Keywords
Keywords;, Cardiovascular disease, Dairy, Inflammation, Blood lipids
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
140 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Dairy diet
Arm Type
Experimental
Arm Title
Control diet
Arm Type
Placebo Comparator
Intervention Type
Other
Intervention Name(s)
Dairy
Other Intervention Name(s)
Dairy products, milk, cheese, yogourt
Intervention Description
During the DAIRY diet, subjects will be asked to incorporate 3 servings of dairy (375 ml of milk, 175 g of yogurt, 30 g of cheese) into their every day diet.
During the CONTROL arm of the study, participants will be asked to consume energy equivalent replacement products (375 ml of fruit juice, 1 homemade cookie, 20 g of cashew).
Primary Outcome Measure Information:
Title
Change in plasma CRP concentrations
Time Frame
At the beginning of the study and the end of the two 4-week diets
Secondary Outcome Measure Information:
Title
Change in endothelial function
Time Frame
At the end of the two 4-week diets
Title
Change in plasma lipid concentrations (LDL-Cholesterol, HDL-C, triglycerides)
Time Frame
At the beginning of the study and the end of the two 4-week diets
Title
Change in insulin levels
Time Frame
At the beginning of the study and the end of the two 4-week diets
Title
Change in anthropometric measures (waist and hip circumferences)
Time Frame
At the beginning of the study and the end of the two 4-week diets
Title
Change in blood pressure
Time Frame
At the begining of the study and the end of the two 4-week diets
Title
Change in CRP intravascular kinetics (in a subsample of the entire study population)
Time Frame
At the end of the two 4-week diets
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Men and women aged between 18 and 70 years
Presenting a subclinical inflammation (Plasma CRP >2 and <10 mg/l)
Abdominal obesity, waist girth >94 cm in men and >80 cm in women
Consumption of dairy products fewer than 2 servings per day
Pre-menopausal women with regular menstrual cycle for the last 3 months
Exclusion Criteria:
Plasma CRP <2 or >10 mg/l
Smokers (>1 cigarette/day)
Body weight variation >10% for the last 6 months prior to the study baseline
BMI >35 kg/m2
Previous history of CVD, type 2 diabetes and monogenic dyslipidemia
Subjects taking medications for hyperlipidemia, hypertension
Post menopausal women who have initiated hormone replacement therapy within 6 months of study onset
Endocrine or gastrointestinal disorders
Smoking
Food allergies, milk aversion or intolerant to lactose
Clinical use of vitamin D or calcium supplements
Vegetarianism
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benoît Lamarche, PhD
Organizational Affiliation
Laval University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Nutraceutical and Functional Foods (INAF), Laval University
City
Quebec
ZIP/Postal Code
G1V 0A6
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
27052530
Citation
Abdullah MM, Cyr A, Lepine MC, Eck PK, Couture P, Lamarche B, Jones PJ. Common Variants in Cholesterol Synthesis- and Transport-Related Genes Associate with Circulating Cholesterol Responses to Intakes of Conventional Dairy Products in Healthy Individuals. J Nutr. 2016 May;146(5):1008-16. doi: 10.3945/jn.115.222208. Epub 2016 Apr 6.
Results Reference
derived
PubMed Identifier
25332474
Citation
Labonte ME, Cyr A, Abdullah MM, Lepine MC, Vohl MC, Jones P, Couture P, Lamarche B. Dairy product consumption has no impact on biomarkers of inflammation among men and women with low-grade systemic inflammation. J Nutr. 2014 Nov;144(11):1760-7. doi: 10.3945/jn.114.200576. Epub 2014 Sep 3.
Results Reference
derived
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Impact of Dairy Consumption on Inflammation: a Clinical Study (PLI)
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