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Effects of Buttermilk on Serum LDL Cholesterol Concentrations

Primary Purpose

Hypercholesterolemia, Buttermilk, Dietary Modification

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Buttermilk without added egg-yolk
Buttermilk with added egg yolk
Skimmed milk with added egg-yolk
Skimmed milk without added egg yolk
Sponsored by
Maastricht University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypercholesterolemia

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged between 18 and 70 years
  • Fasting serum total cholesterol between 5.5 - 8.0 mmol/l
  • Fasting plasma glucose < 7.0 mmol/l
  • BMI between 25-30 kg/m2
  • non-smoking
  • Willingness to abstain for the duration of the study from egg consumption

Exclusion Criteria:

  • unstable body weight (weight gain or loss >3 kg in the past 3 months)
  • allergic for eggs or egg-rich products
  • allergic or intolerant for cow-milk (lactose) based products
  • indication for treatment with cholesterol-lowering drugs according to the Dutch Cholesterol Consensus
  • use of medication or a diet known to affect serum lipid or glucose metabolism - active cardiovascular disease (for instance congestive heart failure) or recent (<6 months) event, such as acute myocardial infarction or cerebro-vascular accident
  • not willing to stop the consumption of vitamin supplements, fish oil capsules or products rich in plant stanol or sterol esters 3 weeks before the start of the study
  • men: consumption of >21 alcohol consumptions a week
  • women: consumption of >14 alcohol consumptions a week
  • abuse of drugs
  • pregnant or breastfeeding women
  • participation in another biomedical study within 1 month prior to the screening visit
  • having donated blood (as blood donor) within 1 month prior to the screening visit or planning to do so during the study
  • impossible or difficult venipuncture as evidenced during the screening visits

Sites / Locations

  • Maastricht University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

Buttermilk with added egg yolk

Buttermilk without added egg-yolk

Skimmed milk with added egg-yolk

Skimmed milk without added egg yolk

Arm Description

Outcomes

Primary Outcome Measures

Change in serum LDL cholesterol concentrations

Secondary Outcome Measures

Changes in serum total and HDL cholesterol, triacylglycerol, apoA-I, apoB and hsCRP concentrations

Full Information

First Posted
March 27, 2012
Last Updated
September 4, 2018
Sponsor
Maastricht University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01566305
Brief Title
Effects of Buttermilk on Serum LDL Cholesterol Concentrations
Official Title
The Effects of Buttermilk With or Without Lutein-enriched Egg Yolk on the Serum LDL Cholesterol Concentration of Slightly Hypercholesterolaemic Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
October 2010 (Actual)
Primary Completion Date
May 1, 2012 (Actual)
Study Completion Date
December 1, 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Rationale and objective: Based on the results of a pilot study, the objective of the present study is to evaluate whether buttermilk lower serum LDL cholesterol concentrations and can prevent the serum LDL cholesterol raising effects of eggs. Study Design: The study has a randomized placebo-controlled factorial 2x2 design. The total study duration is 14 weeks, consisting of a 2 weeks run-in period and a 12 weeks experimental period. Subjects will be stratified for age, gender and BMI over the experimental groups. Study population: One hundred and eight healthy male and female subjects, aged 18-70 years, with slightly elevated serum total cholesterol concentrations (5.5-8.0 mmol/l). Intervention: During the entire study period, volunteers are instructed to consume a diet according to the Dutch dietary guidelines (35 en% fat (10 en% saturated fat), 50-55 en% carbohydrates). During the two weeks run-in period all subjects will drink daily at lunch 100 mL skimmed milk. During the 12 weeks experimental period, a first group of subjects will continue drinking the skimmed milk (control group), while a second group will consume a low-fat buttermilk, a third group skimmed milk enriched with egg-yolk, and a fourth group egg-yolk incorporated into a low-fat buttermilk based beverage. The egg-yolk will be enriched in lutein. Whole egg consumption (others than provided by us) is not allowed during the entire study. Main study parameters/endpoints: Measurements will be performed during the run-in period (days 0, 11 and 14) and during the experimental period (days 56, 95 and 98). The main effects (egg-yolk and buttermilk consumption) will be calculated as the absolute differences between values obtained at the end of the experimental (average days 95 and 98) and run-in (average days 11 and 14) periods. The primary endpoint is the change in serum LDL cholesterol concentrations. Secondary endpoints are changes in serum total and HDL cholesterol, triacylglycerol, apoA-I, apoB and hsCRP concentrations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypercholesterolemia, Buttermilk, Dietary Modification, Cardiovascular Disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
108 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Buttermilk with added egg yolk
Arm Type
Experimental
Arm Title
Buttermilk without added egg-yolk
Arm Type
Experimental
Arm Title
Skimmed milk with added egg-yolk
Arm Type
Experimental
Arm Title
Skimmed milk without added egg yolk
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Buttermilk without added egg-yolk
Intervention Description
Buttermilk without added egg-yolk
Intervention Type
Dietary Supplement
Intervention Name(s)
Buttermilk with added egg yolk
Intervention Description
Buttermilk with added egg yolk
Intervention Type
Dietary Supplement
Intervention Name(s)
Skimmed milk with added egg-yolk
Intervention Description
Skimmed milk with added egg-yolk
Intervention Type
Dietary Supplement
Intervention Name(s)
Skimmed milk without added egg yolk
Intervention Description
Skimmed milk without added egg yolk
Primary Outcome Measure Information:
Title
Change in serum LDL cholesterol concentrations
Time Frame
LDL cholesterol will be measured at day 0, 11, 14, 56, 95 and 98 during the study
Secondary Outcome Measure Information:
Title
Changes in serum total and HDL cholesterol, triacylglycerol, apoA-I, apoB and hsCRP concentrations
Time Frame
Serum total and HDL cholesterol, triacylglycerol, apoA-I and ApoB will be measured at day 0, 11, 14, 56, 95 and 98 during the study. hsCRP concentrations will be measured at day 11, 14, 95 and 98.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged between 18 and 70 years Fasting serum total cholesterol between 5.5 - 8.0 mmol/l Fasting plasma glucose < 7.0 mmol/l BMI between 25-30 kg/m2 non-smoking Willingness to abstain for the duration of the study from egg consumption Exclusion Criteria: unstable body weight (weight gain or loss >3 kg in the past 3 months) allergic for eggs or egg-rich products allergic or intolerant for cow-milk (lactose) based products indication for treatment with cholesterol-lowering drugs according to the Dutch Cholesterol Consensus use of medication or a diet known to affect serum lipid or glucose metabolism - active cardiovascular disease (for instance congestive heart failure) or recent (<6 months) event, such as acute myocardial infarction or cerebro-vascular accident not willing to stop the consumption of vitamin supplements, fish oil capsules or products rich in plant stanol or sterol esters 3 weeks before the start of the study men: consumption of >21 alcohol consumptions a week women: consumption of >14 alcohol consumptions a week abuse of drugs pregnant or breastfeeding women participation in another biomedical study within 1 month prior to the screening visit having donated blood (as blood donor) within 1 month prior to the screening visit or planning to do so during the study impossible or difficult venipuncture as evidenced during the screening visits
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jogchum Plat, Dr.
Organizational Affiliation
Maastricht University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maastricht University
City
Maastricht
State/Province
Limburg
ZIP/Postal Code
6200
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
25456153
Citation
Severins N, Mensink RP, Plat J. Effects of lutein-enriched egg yolk in buttermilk or skimmed milk on serum lipids & lipoproteins of mildly hypercholesterolemic subjects. Nutr Metab Cardiovasc Dis. 2015 Feb;25(2):210-7. doi: 10.1016/j.numecd.2014.10.003. Epub 2014 Oct 13.
Results Reference
derived
Links:
URL
https://doi.org/10.1016/j.numecd.2014.10.003
Description
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Effects of Buttermilk on Serum LDL Cholesterol Concentrations

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