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Metabolic Consequences of Moderate Weight Gain - Role of Dietary Fat Composition (LIPOGAIN)

Not Applicable
Completed
Conditions
Healthy
Interventions
Other: Saturated fatty acid group
Other: 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
Inclusion Criteria
  • Healthy,
  • Body Mass Index 18-27
Exclusion Criteria
  • 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
GroupInterventionDescription
Saturated fatty acid groupSaturated fatty acid groupAddition of saturated fatty acids to the diet inte the form of pastries
Polyunsaturated fatty acid groupPolyunsaturated fatty acid groupAddition of polyunsaturated fatty acids to the diet in the form of pastries
Primary Outcome Measures
NameTimeMethod
Hepatic steatosis by magnetic resonance tomography (MRT)6 weeks
Secondary Outcome Measures
NameTimeMethod
Triglycerides6 weeks
Cholesterol6 weeks
Apolipoprotein B (ApoB)6 weeks
Apolipoprotein A1 (ApoA1)6 weeks
Glucose6 weeks
high density lipoprotein (HDL)6 weeks
low density lipoprotein (LDL)6 weeks
Insulin6 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
Proinsulin6 weeks
Endostatin6 weeks
Pentraxin-3 (PTX-3)6 weeks
Endothelin-1 (ET-1)6 weeks
E-selectin6 weeks
Cathepsin-S6 weeks
Cystatin C6 weeks

Trial Locations

Locations (1)

Uppsala University Hospital, Uppsala Science Park

🇸🇪

Uppsala, Sweden

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