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The Effect of Dairy Fat and Inulin on Fasting Induced Adipose Factor (FIAF) Blood Concentrations

Not Applicable
Completed
Conditions
Obesity
Interventions
Other: Inulin
Other: Complete diet
Other: Whole milk
Registration Number
NCT01913678
Lead Sponsor
University of Copenhagen
Brief Summary

The objective of this study is to investigate whether intake of a diet with a high content of butyrate (from dairy fat) can affect blood FIAF concentration compared to a control diet. Further to examine whether high intake of inulin (a prebiotic) can increase the proportion of butyrate-producing bacteria in the gut and thereby affect blood FIAF concentration. In addition, the correlation between FIAF blood concentrations and resting energy expenditure, blood lipid profile and gut microbiota composition will be investigated.

Furthermore, this study will investigate whether the source of FIAF can be determined. To this end, adipose tissue biopsies will be analyzed and an in vitro experiment with fecal water samples will be carried out.

The study is a crossover randomized controlled trials with 3 arms. Each arm has a duration of 3 weeks. 20 overweight/obese subjects will be enrolled into the study and randomized to the order of interventions. Before and after each intervention period, blood samples will be collected and the participants will have their resting metabolic rate measured. At the end of each intervention period, the participants will collect feces for 5 consecutive days. In addition, adipose tissue biopsies will be taken after each intervention period.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
21
Inclusion Criteria
  • Healthy males
  • Age: 23-45
  • BMI: 25-32 kg/m2
  • Body fat percentage (BFP) > 25
Exclusion Criteria
  • Chronic diseases (known diabetes, cardiovascular disease (CVD), Intestinal Bowel Disease and other chronic diseases likely to affect the results of the present study)
  • Milk allergy/lactose intolerance
  • Intolerance towards inulin
  • Fasting glucose ≥7.0 mmol/l or non-fasting glucose ≥ 11 mmol/l*
  • Use of antibiotics 2 months before commencement of study
  • Use of dietary supplements incl. multivitamins during run-in and the entire study period
  • Smoking
  • Elite athletes (>10 hours of strenuous physical activity per week)
  • Use of prescription medicine which could affect the results of the present study, including systemic glucocorticoids
  • Use of lipid-lowering agents or medication with contraindications for a high fat diet
  • Blood pressure > 140/90 mmHg
  • Blood donation <1 month before study commencement and during study period
  • Simultaneous participation in other clinical studies
  • Inability, physically or mentally, to comply with the procedures required by the study protocol, as evaluated by the study staff

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
InulinInulinThe participants will be given all dietary items in their diet. In the inulin arm, approximately 15 grams of inulin will be included in the diet.
InulinComplete dietThe participants will be given all dietary items in their diet. In the inulin arm, approximately 15 grams of inulin will be included in the diet.
Complete dietComplete dietThe participants will be given all dietary items in their diet.
Whole milkComplete dietThe participants will be given all dietary items in their diet. In the whole milk arm, approximately 1 liter of whole milk will be included in the diet.
Whole milkWhole milkThe participants will be given all dietary items in their diet. In the whole milk arm, approximately 1 liter of whole milk will be included in the diet.
Primary Outcome Measures
NameTimeMethod
Changes in FIAF blood concentration21 days
Secondary Outcome Measures
NameTimeMethod
Changes in gene expression and protein concentration of genes/proteins related to obesity, lipid metabolism, adipocyte differentiation, hypoxia and FIAF signaling in adipose tissue21 days
Changes in blood lipid profile including triglyceride, free fatty acid, low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glycerol, butyrate21 days
Changes in microbiotic composition and characterization of gut microbiota, including metabolites21 days
Changes in resting energy expenditure/lipid oxidation21 days
Changes in short-chain fatty acid content of feces (butyrate, propionate and acetate)21 days
Changes in parameters involved in glucose metabolism21 days
Changes in FIAF adipose tissue messenger ribonucleic acid (mRNA) levels21 days
Changes in FIAF mRNA/protein expressed in or secreted from human intestinal cell lines21 days

Trial Locations

Locations (1)

Department of Nutrition, Exercise and Sports

🇩🇰

Frederiksberg, Copenhagen, Denmark

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