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Clinical Trials/NCT02705560
NCT02705560
Unknown
Not Applicable

Randomized, Controlled, Cross-Over Study to Assess Dietary Biomarkers and Metabolic Effects After a Single Dose of Milk and Cheese in Healthy Subjects

Centre Hospitalier Universitaire Vaudois1 site in 1 country12 target enrollmentAugust 2015
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Centre Hospitalier Universitaire Vaudois
Enrollment
12
Locations
1
Primary Endpoint
Identification of dietary biomarkers of cheese and milk intake
Last Updated
10 years ago

Overview

Brief Summary

Dietary biomarkers are compounds in biofluids that directly reflect the intake of specific foods or food groups. Their exploration and use in the field of dietary assessments could provide an objective measure of actual intake complementing classical assessment methods (e.g. food frequency questionnaire, 24h recalls). To date, only a limited number of foods have been covered by validated biomarkers.

The study is part of the international project "The Food Biomarker Alliance (FOODBALL)". The study described here has been assigned to assess biomarkers of the intake of milk and cheese. Up to now, there is an evident lack of data on specific and validated biomarkers of milk and cheese (dairy products), which belong to the most relevant public health related foods in Europe. This study will further provide novel insights into the influence of fermentation of milk-based foods on metabolic effects and postprandial adaptations, which has not yet been studied in depth before using cheese as fermented product. Outcomes will support and expand earlier findings on correlation between the intake of fermented dairy products intake and human health.

Detailed Description

This is an acute, randomized, controlled, cross-over study designed to identify dietary biomarkers of milk and cheese intake and to asses metabolic effects after the ingestion of a non-fermented product (milk) and a fermented product (cheese) in healthy subjects. Twelve healthy participants (six women, six men) in fasted state will consume three different foods in a randomized order on three different study days. Two days prior to each dietary intervention, the run-in period is initiated, during which participants have to follow a restricted diet. Participants will receive a standardised meal for the last dinner during run-in phase. The same meal will be served on the day of the dietary intervention for lunch and for dinner (period of controlled diet). Before and after ingestion of the test foods, blood samples and urine samples will be collected (up to 6 hours). Additionally, 24h-samples will be collected. Primary outcomes (metabolites) will be measured in blood serum and plasma collected at 6 different time points and in urine collected at 7 different time points. Transcriptomics analysis will be performed on whole blood samples collected at 4 time points while clinical chemistry parameters will be assessed in blood samples withdrawn at 6 different time points.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
May 2018
Last Updated
10 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Francois Pralong

Prof, MD

Centre Hospitalier Universitaire Vaudois

Eligibility Criteria

Inclusion Criteria

  • Healthy males and females
  • Aged 18 - 40 years
  • BMI \> 18.5 and \< 30 kg/m2
  • Daily consumption of milk
  • No adverse effects after intake of 600 ml of milk

Exclusion Criteria

  • Diagnosed health condition (chronic or infectious disease)
  • Taking medication (oral contraceptive pill is allowed)
  • Taking nutritional supplements (e.g. vitamins, minerals)
  • Pregnant, lactating
  • Antibiotics treatment 6 months prior to intervention
  • Allergy to milk
  • Allergy to soy
  • Known intolerance to lactose
  • Other food allergies or intolerances (e.g. histamine)
  • Anemia (hemoglobin \< 120 g/l) at the screening visit

Outcomes

Primary Outcomes

Identification of dietary biomarkers of cheese and milk intake

Time Frame: 24 hours

Secondary Outcomes

  • LDL cholesterol(24 hours)
  • Glucose(24 hours)
  • Triacylglycerides(24 hours)
  • HDL cholesterol(24 hours)
  • Transcriptomics analyses / gene expression(6 hours)
  • Blood cell count and cell type determination(6 hours)
  • Insulin(24 hours)
  • Total cholesterol(24 hours)

Study Sites (1)

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