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Acute Fatty Acid Intervention Study (AFAST)

Acute Fatty Acid Intervention Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01000194
Acronym
AFAST
Enrollment
21
Registered
2009-10-22
Start date
2008-01-31
Completion date
2008-03-31
Last updated
2009-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease, The Metabolic Syndrome

Keywords

postprandial, gene expression profiles, microarray

Brief summary

The main objective of this study is to elucidate whether different dietary fatty acids (SFA, PUFA, butter fat and margarine fat) in a high fat load will have different effects on PBMC gene expression profiles. Secondary objectives are to elucidate the effects of these fat loads on individual plasma free fatty acid profiles, triglycerides and cholesterol levels.

Detailed description

Nutrition plays a key role in the development of metabolic disorders like cardiovascular disease and the metabolic syndrome. Nutrients that can contribute to the risk of developing such diseases are fatty acids (FAs). It is known that fatty acids mediate their metabolic effects via changes in gene expression, through binding and subsequent activation of the transcription factor peroxisome proliferator-activated receptor (PPAR). In addition, it is known that unsaturated fatty acids are better ligands for PPAR than saturated fatty acids. Peripheral blood mononuclear cells (PBMC) express PPARalpha and are relatively easy to isolate from whole blood. We previously showed that the gene expression profiles of these cells can reflect free fatty acid increases during fasting. The question still remains whether dietary FA can influence gene expression in a similar way and, if so, whether different dietary FA result in different gene expression changes and subsequent activation of other pathways.

Interventions

DIETARY_SUPPLEMENTHigh fat meal

A high fat milkshake containing 55g of fat

Sponsors

Dutch Dairy Organization (NZO)
CollaboratorOTHER
Wageningen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy Caucasian men * age between 18 and 30 years

Exclusion criteria

* Allergic to fish oil * Allergic to margarine * Allergic to cow milk or dairy products * Current or recent (\<4 weeks) use of fish oil supplements or more then four times fish/week; 24.35 g of EPA-DHA of fish per month (800 mg/day) as judged by the questionnaire. * Body mass index (BMI) \< 18 or \> 25 kg/m2 * Urine glucose concentrations outside normal ranges (low to non-detectable) * Fasting blood glucose outside the normal range (3 - 5.5 mmol/L) * Tobacco smoking * Taking medication that may influence the study results * Received inoculations within 2 months of starting the study or planned to during the study * Donated or intended to donate blood from 2 months before the study till two months after the study * Diagnosed with any long-term medical condition (eg., diabetes, hemophilia, cardiovascular disease, anemia, gastrointestinal disease) * Vegetarian

Design outcomes

Primary

MeasureTime frame
Peripheral blood mononuclear cells (PBMC) gene expression profiles0, 2, 4, 6, 8 hours

Secondary

MeasureTime frame
Plasma free fatty acid profiles0, 6 hours
Plasma free fatty acids0, 2, 4, 6, 8 hours
Plasma cholesterol0, 2, 4, 6, 8 hours
Plasma triglycerides0, 2, 4, 6, 8 hours

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026