Looking for Personalized Nutrition for Obesity/Type 2 Diabetes Mellitus Prevention
- Conditions
- Diet ModificationGenetic PredispositionDiabetes Mellitus, Type 2Overweight and ObesityMetabolic Syndrome
- Interventions
- Other: Normo-carbohydrate meal intakeOther: High-carbohydrate meal intakeOther: High-fat meal intakeOther: High-protein meal intake
- Registration Number
- NCT03792685
- Lead Sponsor
- Medical University of Bialystok
- Brief Summary
The objectives of this trial are to assess the effects of interactions between genetic factors and diet with various macronutrient intake on the metabolic disorders, obesity and type 2 diabetes risk, prevention, development and progress.
- Detailed Description
This is a randomized, crossover study that includes 1 screening visit and four meal challenge test visits, separated by a 1-2-weeks washout period. The screening will include 2000 people, males and females, to evaluate the genotype frequencies in studied population, and to find carriers of the rare genetic single nucleotide polymorphisms (SNPs), who will fulfill all the other inclusion criteria. An oral glucose tolerance test (OGTT) will be completed at screening visit. Moreover, the fasting blood samples will be collected for genetic analysis, and measurements of blood glucose and lipid metabolism profile, high-sensitivity C-reactive protein (hs-CRP), hormones/peptides and other factors involved in energy balance regulation. Subjects will be asked to record their daily food intake for 3 days. Assessments of vital signs and body height and weight, waist and hip circumferences, body fat content and body fat distribution, review of concomitant medication/supplement use and inclusion and exclusion criteria, and evaluation of adverse effects will be performed throughout the study. To meal challenge test only men will be included, since the sex hormones may influence the study endpoints. Subjects will be encouraged to maintain their habitual diet during wash-out periods. During the each meal challenge test subjects will consume one of the study meals in random order. The blood will be collected at fasting state and 30, 60, 120, 180 and 240 minutes after meal intake. The energy expenditure and substrate utilization will be measured by indirect calorimetry method at the fasting and postprandially.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 150
- healthy men with normal body weight and with overweight/obesity
- men with metabolic syndrome, hypertension, type 2 diabetes newly diagnosed, or not treated with any medicines
- maintaining the usual diet and lifestyle throughout the study
- infectious or acute diseases in the last 4 weeks before the study visits
- any medicines/dietary supplements consumption in the last 4 weeks before the study visits
- high level of daily physical activity
- the following any special diet or dietary patterns (vegetarian, high-fat etc.)
- the presence of any other significant disease which may affect the results (hormonal disorders, history of any surgeries on gastrointestinal tract, allergies known or suspected, heart failure, history of cancer, any kidney, pancrea and liver diseases, except non-alcoholic fatty liver)
- abusive alcohol consumption
- abusive coffee or energy drinks consumption
- drug consumption
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Normal weight High-protein meal intake Normal weight men. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Normal weight High-fat meal intake Normal weight men. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Normal weight Normo-carbohydrate meal intake Normal weight men. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Diabetes High-carbohydrate meal intake Men with prediabetes or type 2 diabetes mellitus. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Overweight/obesity High-carbohydrate meal intake Men with overweight or obesity. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Normal weight High-carbohydrate meal intake Normal weight men. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Overweight/obesity High-protein meal intake Men with overweight or obesity. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Diabetes Normo-carbohydrate meal intake Men with prediabetes or type 2 diabetes mellitus. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Overweight/obesity Normo-carbohydrate meal intake Men with overweight or obesity. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Diabetes High-protein meal intake Men with prediabetes or type 2 diabetes mellitus. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Overweight/obesity High-fat meal intake Men with overweight or obesity. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake. Diabetes High-fat meal intake Men with prediabetes or type 2 diabetes mellitus. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake.
- Primary Outcome Measures
Name Time Method The postprandial change and differences in serum insulin concentrations associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in serum insulin concentrations (IU/mL) will be evaluated, dependently on the meal type, genetic and metabolic (body weight, body fat content)
The change and differences in postprandial Free Fatty Acids (FFAs) concentrations associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in blood FFAs (umol/L) concentrations will be evaluated, dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The change and differences in postprandial energy expenditure levels associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in energy expenditure levels (kcal/min) will be evaluated by indirect calorimetry method, dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The change and differences in postprandial substrates (carbohydrate, fat and protein) utilization levels associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in substrates (carbohydrate, fat and protein) utilization (mg/min) will be evaluated by indirect calorimetry method, dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The change and differences in postprandial Triglycerides (TGs) concentrations associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in blood TGs (mg/dL) concentrations will be evaluated, dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The postprandial change and differences in blood glucose levels associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in blood glucose concentrations (mg/dL) will be evaluated, dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
- Secondary Outcome Measures
Name Time Method The change and differences in postprandial leptin concentrations associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in blood leptin concentrations (ng/mL) will be evaluated dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The change and differences in postprandial plasma metabolites profiles associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180 minutes after meal intake. The postprandial change and differences in plasma metabolites profiles (metabolomic fingerprinting) will be evaluated dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The change and differences in postprandial peptide YY (PYY) concentrations associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180 minutes after meal intake. The postprandial change and differences in blood PYY (pg/mL) concentrations will be evaluated dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The change and differences in postprandial ghrelin concentrations associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in blood ghrelin concentrations (pg/mL) will be evaluated dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
The change and differences in postprandial adiponectin concentrations associated with investigated single nucleotide polymorphisms. Fasting (time 0) and 30, 60, 120, 180, 240 minutes after meal intake. The postprandial change and differences in blood adiponectin concentrations (ng/mL) will be evaluated dependently on the meal type, genetic and metabolic (body weight, body fat content) factors.
Trial Locations
- Locations (1)
Clinical Research Centre, Medical University of Bialystok
🇵🇱Bialystok, Polska, Poland