a low concentration of the protective ('good') cholesterol Low HDL cholesterol
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • aged between 45 and 70 years • HDL-C
Exclusion criteria
Exclusion criteria: • unstable body weight (weight gain or loss >3 kg in the past 3 months) • indication for treatment with cholesterol-lowering drugs according to the Dutch Cholesterol Consensus • use of medication or a medically-prescribed diet known to affect serum lipid or glucose metabolism. Oral anti-contraceptives and paracetamol are allowed. • Active cardiovascular disease (for instance congestive heart failure) or recent (21 glasses of alcohol-containing drinks per week women: consumption of >14 glasses of alcohol-containing drinks per week • abuse of drugs • pregnant or breastfeeding women • participation in another biomedical study within 1 month prior to the screening visit • having donated blood (as blood donor) within 1 month prior to the screening visit or planning to do so during the study • impossible or difficult to puncture as evidenced during the screening visits
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the change in serum apoA-I concentrations and serum HDL-C. | — |
Secondary
| Measure | Time frame |
|---|---|
| -flow-mediated dilation -pulse wave velocity -glucose- en insulineconcentration -ApoB -Total cholesterol -LDL-C -Triglycerides -hdCRP -IL-6 -sICAM-1 -VCAM-1 -MCP-1 -sE Selectin - Blood chemistry: phosphorus, sodium, potassium, chloride, calcium, creatinine, blood urea nitrogen (BUN), protein, albumin, gammaGT, aspartate-aminotransferase (AST), alanine-aminotransferase (ALT), alkaline phosphatase (ALP), bilirubin - Haematology: White cell count, red cell count, platelet count, hemoglobin, hematocrit, mean cell volume, and mean cell hemoglobin concentration, red cell distribution - Blood coagulation: Prothrombin time (PT) and aPT | — |
Countries
Netherlands