Metabolic Syndrome, Syndrome X, Insulin Resistance Syndrome Metabolic Syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Men and women, aged between 45-75 years- Women postmenopausal: two or more years after last menstruation- Fasting plasma glucose < 7.0 mmol/L- Fasting serum total cholesterol < 8.0 mmol/L- Fasting serum triacylglycerol < 4.5 mmol/L- Systolic blood pressure < 160 mmHg and diastolic blood pressure < 100 mmHg- Stable body weight (weight gain or loss < 3 kg in the past three months)- Willingness to give up being a blood donor from 8 weeks before the start of the study, during the study and for 4 weeksafter completion of the study- No difficult venipuncture as evidenced during the screening visit
Exclusion criteria
Exclusion criteria: - Allergy or intolerance to peanuts- Left-handedness (effects on brain health differ between left- and right-handed adults)- Current smoker, or smoking cessation < 12 months- Diabetic patients - Familial hypercholesterolemia- Abuse of drugs- More than 3 alcoholic consumptions per day- Use of products or dietary supplements known to interfere with the main outcomes as judged by the principal investigators- Use of medication to treat blood pressure, lipid, or glucose metabolism - Use of an investigational product within another biomedical intervention trial within the previous 1-month- Severe medical conditions that might interfere with the study, such as epilepsy, asthma, kidney failure or renal insufficiency, chronic obstructive pulmonary disease, inflammatory bowel diseases, auto inflammatory diseases, and rheumatoid arthritis- Active cardiovascular disease like congestive heart failure or cardiovascular event, such as an acute myocardial infarction or cerebrovascular accident- Contra-indications for MRI imaging (e.g., pacemaker, surgical clips/material in body, metal splinter in eye, claustrophobia)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the difference at follow-up in the cerebral blood flow response between peanut butter intervention and control periods. | — |
Secondary
| Measure | Time frame |
|---|---|
| Cognitive performance will be assessed, while we will also focus on appetite-related brain reward activity. | — |
Countries
Netherlands
Contacts
Universiteit Maastricht