Diabetes Mellitus, Type 2, Cardiovascular Disease
Conditions
Keywords
Moderate alcohol consumption, Fat and carbohydrate oxidative capacity, Postprandial glycemic response
Brief summary
Moderate alcohol consumption is associated with a decreased risk of diabetes type 2. This association could be mediated by an improvement of insulin sensitivity with moderate alcohol consumption. Patients with diabetes type 2 or impaired glucose tolerance often may have decreased fat oxidative capacity or oxidative phosphorylation in tissue such as muscle. This could lead to accumulation triglyceride storage in muscle, which could interfere with insulin signaling. Whether such mechanism can also play a role with moderate alcohol consumption is unknown and will be investigated in this study. In addition, moderate alcohol consumption with a meal can lead to delayed hypoglycemia in type 1 diabetes patients. How moderate alcohol consumption affects postprandial glycemic response in healthy subjects is unknown. This is a secondary objective of this trial.
Detailed description
To investigate the effect of moderate alcohol consumption on * enzymes involved in fatty acid oxidation, oxidative phosphorylation and glycolysis in skeletal muscle * transporters of fatty acids and glucose in fat tissue * post-prandial glycemic response in healthy, lean or overweight, young men Design : Open, randomized, partially diet-controlled, placebo controlled cross-over design Participants * Description : Healthy, lean and overweight young (18-40 years) men * Number : 20 Study substances * Test substance : 100 ml whiskey (Famous Grouse, 40% v/v alcohol: ≈ 32 g alcohol) * Reference substance : 100 ml mineral water (Spa blauw) Duration: 2 treatment periods of 4 weeks (28 days) Test parameters: * Muscle biopsy for activity of 3-hydroxy fatty-acyl CoA dehydrogenase, citrate synthase, cytochrome c oxidase * Postprandial glycemic response (glucose, insulin, GLP-1, GLP-2, GIP, glucagon, FFA etc.) * Insulin sensitivity and related factors (oral glucose tolerance test, adiponectin, HbA1c) * Liver enzymes (safety) * Body weight * Urinary ethyl glucuronide (compliance)
Sponsors
Dutch Foundation for alcohol research
TNO
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to 40 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy men aged between 18 and 40 years * Lean subjects BMI 18.5-25 kg/m2 and overweight/obese subjects BMI \>27 kg/m2 (including 18.5, 25 and 27) * Alcohol consumption between 7 and 28 units/week (including 7 and 28)
Exclusion criteria
* Smoking * Family history of alcoholism * History of medical or surgical events that may significantly affect the study outcome, particularly metabolic or endocrine disorders and gastrointestinal disorders * Recent blood donation * More than 8 hours/week of intense exercise * Blood haemoglobin concentration below 8.4 mmol/l * Allergic to betadine or lidocaine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| enzymes involved in fatty acid oxidation, oxidative phosphorylation and glycolysis in skeletal muscle | 4 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Post-prandial glycemic response | 4 weeks |
| insulin sensitivity (oral glucose tolerance test) and related factors (adiponectin, HbA1c) | 4 weeks |
Outcome results
None listed