Metabolic Consequences of Moderate Weight Gain - Role of Dietary Fat Composition (LIPOGAIN)
- Conditions
- Healthy
- Interventions
- Other: Saturated fatty acid groupOther: Polyunsaturated fatty acid group
- Registration Number
- NCT01427140
- Lead Sponsor
- Uppsala University
- Brief Summary
The purpose of this study is to investigate the metabolic consequences of a moderate weight gain and if the type of dietary fat (saturated versus polyunsaturated) can modify the effects in young healthy adults. Hypothesis: the type of dietary fat can modify the effects of weight gain.
- Detailed Description
Specific goals:
* Investigate if dietary fat composition influences liver fat accumulation and metabolic risk factors in response to moderate weight gain
* Investigate if polyunsaturated fat (PUFA) in the diet could counteract any unfavorable metabolic changes that are expected to accompany moderate weight gain
* Investigate effects of weight gain and dietary fat composition on markers of vascular health
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 41
- Healthy,
- Body Mass Index 18-27
- Liver disease,
- Coronary heart disease,
- Diabetes mellitus,
- Malignant diseases,
- Alcohol or drug abuse,
- Magnetic Resonance-incompatibility,
- Abnormal clinical chemistry,
- Use of drugs that significantly effects energy metabolism,
- Heavy exercise,
- Pregnancy or lactation,
- Allergy of gluten, egg or milk protein
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Saturated fatty acid group Saturated fatty acid group Addition of saturated fatty acids to the diet inte the form of pastries Polyunsaturated fatty acid group Polyunsaturated fatty acid group Addition of polyunsaturated fatty acids to the diet in the form of pastries
- Primary Outcome Measures
Name Time Method Hepatic steatosis by magnetic resonance tomography (MRT) 6 weeks
- Secondary Outcome Measures
Name Time Method Triglycerides 6 weeks Cholesterol 6 weeks Apolipoprotein B (ApoB) 6 weeks Apolipoprotein A1 (ApoA1) 6 weeks Glucose 6 weeks high density lipoprotein (HDL) 6 weeks low density lipoprotein (LDL) 6 weeks Insulin 6 weeks Aspartate aminotransferase (ASAT) 6 weeks Alanine aminotransferase (ALAT) 6 weeks Gamma glutamyl transpeptidase (GGT) 6 weeks Homeostasis model of assessment insulin resistance (HOMA-IR) 6 weeks C-reactive protein (CRP) 6 weeks Proinsulin 6 weeks Endostatin 6 weeks Pentraxin-3 (PTX-3) 6 weeks Endothelin-1 (ET-1) 6 weeks E-selectin 6 weeks Cathepsin-S 6 weeks Cystatin C 6 weeks
Trial Locations
- Locations (1)
Uppsala University Hospital, Uppsala Science Park
🇸🇪Uppsala, Sweden