Acetylcarnitine and Metabolic Flexibility

NCT ID: NCT02072759

Last Updated: 2016-07-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-03-31
• Study Completion Date: 2016-06-30

Brief Summary

Insulin resistant subjects and type 2 diabetic patients are characterized by a decreased metabolic flexibility: a reduced capability to switch from fat oxidation in the basal state to carbohydrate oxidation in the insulin-stimulated state. This metabolic inflexibility is an early hallmark in the development of diabetes. Recent evidence suggests that a low carnitine availability may limit acetylcarnitine formation, thereby reducing metabolic flexibility. We propose to test the hypothesis that metabolic inflexibility in pre-diabetic subjects and diabetic patients is due to a reduced capacity to form acetylcarnitines.

Detailed Description

Background: Insulin resistant subjects and type 2 diabetic patients are characterized by a decreased metabolic flexibility: a reduced capability to switch from fat oxidation in the basal state to carbohydrate oxidation in the insulin-stimulated state. This metabolic inflexibility is an early hallmark in the development of diabetes. Recent evidence suggests that low carnitine availability may limit acetylcarnitine formation, thereby reducing metabolic flexibility.

Objectives: We will investigate whether subjects with impaired glucose tolerance (IGT) show a diminished capacity to form acetylcarnitine in the face of high substrate availability. Therefore, we will use a novel non-invasive 1H-Magnetic Resonance Spectroscopy (1H-MRS) protocol to determine in vivo, and in time, the formation of acetylcarnitine in skeletal muscle. Additionally, we will examine whether carnitine supplementation increases the capacity to form acetylcarnitine and improves metabolic flexibility and insulin sensitivity in IGT subjects.

Study design: 12 subjects with IGT will be included and will be subjected to either placebo- or carnitine treatment (daily capsules with 2g of L-carnitine or placebo) in a randomized, placebo-controlled, double blind crossover design. After both interventions, acetylcarnitine formation after a mixed meal will be determined by 1H-MRS and meal-induced changes in fat and glucose oxidation by indirect calorimetry. The maximal acetylcarnitine formation will be measured after a cycling test via 1H-MRS. A hyperinsulinemic-euglycemic clamp will be performed to determine insulin sensitivity. Biopsies will be taken to measure free carnitine and carnitine acetyltransferase (CrAT) activity. To investigate whether differences in acetylcarnitine formation may be involved in variations in glucose tolerance, twelve control subjects, matched for BMI and age but glucose tolerant (based on oral glucose tolerance test, according to WHO criteria) will also be included and will undergo all measurements once without any intervention.

Conditions

Glucose Intolerance

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

Carnitine supplement

Carnitine supplement

Group Type: EXPERIMENTAL

Carnitine supplement

Intervention Type: DIETARY_SUPPLEMENT

Carnitine supplement (oral ingestion with meals)

Total dosage of 2g carnitine per day for 36 days.

• 1 carnitine supplement at breakfast (500mg)
• 1 carnitine supplement at lunch (500mg)
• 2 carnitine supplements at diner (2x 500mg=1000mg)

Placebo

Placebo supplement

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DIETARY_SUPPLEMENT

Healthy control

Healthy control group

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Carnitine supplement

Carnitine supplement (oral ingestion with meals)

Total dosage of 2g carnitine per day for 36 days.

• 1 carnitine supplement at breakfast (500mg)
• 1 carnitine supplement at lunch (500mg)
• 2 carnitine supplements at diner (2x 500mg=1000mg)

Intervention Type: DIETARY_SUPPLEMENT

Placebo

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• Age 40-70 years
• Overweight/obese, BMI 25-35 kg/m2
• Stable dietary habits
• Generally healthy with no medication use that interferes with metabolism

Exclusion Criteria

• Fasting plasma glucose >7.1 mmol/l
• Haemoglobin <7.8 mmol/l
• Hypertension: blood pressure > 140 mmHg systolic or 90 mmHg diastolic
• Cardiac problems, such as angina pectoris, cardiac infarction and arrhythmias
• Plasma creatinine concentration higher than 115 micromol/l (in men) en 100 micromol (in women).
• Any medical condition requiring treatment and/or medication that interferes with investigated parameters
• Unstable body weight (weight gain or loss > 3 kg in the past three months)
• Participation in another biomedical study within 1 month prior to the screening visit
• Subjects with contra-indication for MRI
• Subjects, who do not want to be informed about unexpected medical findings, or do not wish that their treating physician is informed, cannot participate in the study.
• Subject are not allowed to donate blood three months prior to the start of the study and three months after finishing the study.

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

European Foundation for the Study of Diabetes

OTHER

Sponsor Role: collaborator

Maastricht University Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Vera B Schrauwen, PhD

Role: PRINCIPAL_INVESTIGATOR

Maastricht University Medical Center

Locations

Maastricht University Medical Center

Maastricht, Limburg, Netherlands

Countries

Netherlands

Other Identifiers

NL44572.068.13

Identifier Type: -

Identifier Source: org_study_id