Looking for Personalized Nutrition for Obesity/Type 2 Diabetes Mellitus Prevention

Sponsor
Medical University of Bialystok (Other)
Overall Status
Completed
CT.gov ID
NCT03792685
Collaborator
Ministry of Science and Higher Education, Poland (Other)
150
1
3
135.3
1.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Normo-carbohydrate meal intake
  • Other: High-carbohydrate meal intake
  • Other: High-fat meal intake
  • Other: High-protein meal intake
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
Analysis of Genetic Aspects of Metabolic Response on Diet With Different Content of Carbohydrate and Fat. Searching for Genetic Markers for Individualized Therapy in Patients With Obesity and Type 2 Diabetes
Actual Study Start Date :
Sep 24, 2009
Actual Primary Completion Date :
Jun 1, 2020
Actual Study Completion Date :
Jan 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Normal weight

Normal weight men. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake.

Other: Normo-carbohydrate meal intake
Subjects are going to receive the normo-carbohydrate meal.

Other: High-carbohydrate meal intake
Subjects are going to receive the high-carbohydrate meal.

Other: High-fat meal intake
Subjects are going to receive the high-fat meal.

Other: High-protein meal intake
Subjects are going to receive the high-protein meal.

Experimental: Overweight/obesity

Men with overweight or obesity. Interventions: normo-carbohydrate meal intake, high-carbohydrate meal intake, high-fat meal intake, high-protein meal intake.

Other: Normo-carbohydrate meal intake
Subjects are going to receive the normo-carbohydrate meal.

Other: High-carbohydrate meal intake
Subjects are going to receive the high-carbohydrate meal.

Other: High-fat meal intake
Subjects are going to receive the high-fat meal.

Other: High-protein meal intake
Subjects are going to receive the high-protein meal.

Experimental: Diabetes

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.

Other: Normo-carbohydrate meal intake
Subjects are going to receive the normo-carbohydrate meal.

Other: High-carbohydrate meal intake
Subjects are going to receive the high-carbohydrate meal.

Other: High-fat meal intake
Subjects are going to receive the high-fat meal.

Other: High-protein meal intake
Subjects are going to receive the high-protein meal.

Outcome Measures

Primary Outcome Measures

  1. 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.

  2. 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)

  3. 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.

  4. 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.

  5. 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.

  6. 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.

Secondary Outcome Measures

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 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

Exclusion Criteria:
  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinical Research Centre, Medical University of Bialystok Bialystok Polska Poland 15-276

Sponsors and Collaborators

  • Medical University of Bialystok
  • Ministry of Science and Higher Education, Poland

Investigators

  • Study Director: Edyta Adamska-Patruno, PhD, Clinical Research Centre, Medical University of Bialystok
  • Principal Investigator: Maria Gorska, Prof., Dept of Endocrinology, Diabetology and Internal Medicine
  • Principal Investigator: Adam Kretowski, Prof., Dept of Endocrinology, Diabetology and Internal Medicine; Clinical Research Centre

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical University of Bialystok
ClinicalTrials.gov Identifier:
NCT03792685
Other Study ID Numbers:
  • N N402 477437
First Posted:
Jan 3, 2019
Last Update Posted:
Feb 21, 2021
Last Verified:
Feb 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 21, 2021