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Hepatic Insulin Sensitivity and Very Low Density Lipoprotein Triglyceride (VLDL-TG) Kinetics

Not Applicable
Completed
Conditions
Obesity
Dyslipidemia
Interventions
Other: Glucose clamp
Registration Number
NCT01205750
Lead Sponsor
University of Aarhus
Brief Summary

Obesity is associated with dyslipidemia, which is a major risk factor for coronary heart disease. Triglycerides (TG) and cholesterol are transported in the system of lipoproteins, and the metabolism of these lipids in plasma is closely interrelated. Evidence suggests that increased concentration of very low-density lipoprotein triglyceride (VLDL-TG) is a central pathophysiological feature of the lipid and lipoprotein abnormalities in dyslipidemia.

The primary objective of this study is to investigate VLDL-TG kinetics and hepatic insulin sensitivity in age-matched obese and lean, healthy men in the postabsorptive state and during acute hyperinsulinemia using VLDL-TG and glucose tracers.

Detailed Description

Extensive description not included.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
24
Inclusion Criteria
  • Healthy
  • BMI < 25 kg/m2 or > 30 kg/m2
  • Informed consent
Exclusion Criteria
  • Alcohol misuse
  • Smoking
  • Use of prescription drugs

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Glucose clampGlucose clamp-
Primary Outcome Measures
NameTimeMethod
VLDL-TG kineticsVLDL-TG kinetics are determined postabsorptively (250 minues) and during acute hyperinsulinemia (450 minutes)

VLDL-TG secretion rates(umol/min) and clearance rates (ml/min)are determined during 30 min steady state periods postabsorptively and using acute hyperinsulinemia using primed-constant infusion of ex vivo-labelled 14C-VLDL-TG tracer and traditional tracer dilution technique.

Secondary Outcome Measures
NameTimeMethod
Hepatic insulin sensitivityGlucose kinetics are determined postabsorptively (250 minues) and during acute hyperinsulinemia (450 minutes)

Hepatic glucose production (mg/min) is determined during 30 min steady state periods postabsorptively and during acute hyperinsulinemia using primed constant infusion og 3H-glucose tracer and traditional tracer dilution technique.

Trial Locations

Locations (1)

Department of Endocrinology and Internal Medicine, Aarhus University Hospital

🇩🇰

Aarhus, Denmark

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