Obesity Clinical Trial
Official title:
Ernährungs-Interventions-Fettleber-Studie (Interventional Study on Nutritional Effects on NAFLD)
Epidemiological data and studies in animal models suggest, that polyunsatured fatty acids
(PUFA) rather than mono-unsatured fatty acids (MUFA) are associated with lower hepatic lipid
content (HCL) and may facilitate a decrease of HCL in case of non-alcoholic fatty liver
disease (NAFLD).
The investigators therefore conduct an interventional trial in subjects with normal glucose
metabolism, but increased HCL, fulfilling criteria for NAFLD.
The study will compare two dietary interventions in parallel design, one containing mainly
PUFA (canola oil), one containing only MUFA (olive oil). The intervention of 8 weeks is
accomodated by dietary counseling. Metabolic outcome variables will be assessed with MR
spectroscopy (liver fat) and euglycemic hepatic clamp (glucose metabolism/insulin
sensitivity).
Epidemiological data and studies in animal models suggest, that polyunsatured fatty acids
(PUFA) rather than mono-unsatured fatty acids (MUFA) are associated with lower hepatic lipid
content (HCL) and may facilitate a decrease of HCL in case of non-alcoholic fatty liver
disease (NAFLD). A typical source for PUFAs are fish and certain plant oils, a source of
almost pure MUFAs is olive oil.
The investigators therefore conduct an interventional trial in subjects with normal glucose
metabolism, but increased HCL, fulfilling criteria for NAFLD. The investigation focusses on
male participants to avoid sex-related differences in the results.
The study will compare two isocaloric dietary interventions in parallel design, one
containing mainly PUFA (canola oil), one containing only MUFA (olive oil). The intervention
of 8 weeks is accomodated by dietary counseling (4 sessions). Metabolic outcome variables
will be assessed with MR spectroscopy (liver fat), anthropometry (to check for stable weight
and body composition) and euglycemic hepatic clamp (glucose metabolism/insulin sensitivity).
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator), Primary Purpose: Treatment
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