Markers of Appetite Regulation During Exogenous Ketosis - a Placebo Controlled Randomized Study of Appetite Regulatory and Metabolic Markers After Intake of a Keto- or Glucogenic Drink.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Ketosis
- Sponsor
- Central Jutland Regional Hospital
- Enrollment
- 10
- Locations
- 1
- Primary Endpoint
- GLP-1 concentration
- Last Updated
- 6 years ago
Overview
Brief Summary
The aim of this study is to investigate the relationship, if any, between markers of satiety, desire to eat, hunger, and metabolic markers of the regulation hereof during ketosis as compared with a Glucose-containing and a Placebo drink adjusted for taste.
Detailed Description
All subjects are, in random order, tested on three separate occasions with intake of weight adjusted and taste matched drink of i) a ketone ester, and ii) an isocaloric and -volumetric glucose drink, or iii) an isovolumetric tap water drink. Subjects are studied for five hours with baseline and blood sampling on multiple occasions. A satiety questionaire are included. Subjects are recruited through notice on website for this purpose. Sample size calculations were performed prior to inclusion (n=10). According to protocolized statistical plan, missing data will not be replaced and no imputation will occur. Data will be analyzed by applying a repeated measurements multilevel model with intervention, time and their interactions as categorical factors. Effects size are adjusted for small sample size.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Males aged 18-65 years
- •BMI 20-35 kg/m2
- •Expected ease of catheter insertion
- •Oral and written informed consent
Exclusion Criteria
- •Inability to fully understand the consent including consent forms
- •Inability to cooperate to the trial
- •Any electrolyte disorders, kidney disease or otherwise compromised renal function including excess risk hereof, e.g. hypertension, albuminuria, autoimmune disease, family history of kidney disease
- •Any liver or bile disease including excess risk hereof, e.g. hepatotoxic drugs, alcohol abuse disorder, gallstones, pancreatitis, autoimmune disease, family history of liver disease
- •Diabetes mellitus or any metabolic and/or hormonal disease including diagnosed/undiagnosed reactive hypoglycemia or similar disorders. This includes treatment with drugs, dietary supplement with inference on key metabolic or hormonal markers, e.g. insulin, glukagon, lipids, and GLP-1
- •Any use of illegal or otherwise use of medicinal products without prescription
- •Anemia or other know disease of the hematopoietic system
- •Previous bariatric surgery
- •Previous myocardial infarction or uncontrolled myocardial ischemia
- •Recent intended/unintended weight loss
Outcomes
Primary Outcomes
GLP-1 concentration
Time Frame: 5 hours
Development of GLP-1 concentration during ketosis as compared after intake of a ketogenic vs a glucogenic drink vs a control drink, respectively.
Acyl ghrelin concentration
Time Frame: 5 hours
Development of acyl ghrelin concentration during ketosis as compared after intake of a ketogenic vs a glucogenic drink vs a control drink, respectively.
Secondary Outcomes
- Satiety, desire to eat, and perceived hunger sensation(5 hours)
- Insulin concentration(5 hours)
- Glucose concentration(5 hours)
- Free fatty acids concentration(5 hours)