Metabolic Phenotyping in Humans (MetPhe)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2012 by Maastricht University Medical Center.
Recruitment status was  Recruiting
Sponsor:
Information provided by (Responsible Party):
Maastricht University Medical Center
ClinicalTrials.gov Identifier:
NCT01298375
First received: February 16, 2011
Last updated: July 18, 2012
Last verified: July 2012

February 16, 2011
July 18, 2012
March 2011
March 2013   (final data collection date for primary outcome measure)
Euglycemic-hyperinsulinemic clamp for measurement of insulin sensitivity and metabolic flexibility [ Time Frame: 10 hours ] [ Designated as safety issue: Yes ]
After taking fasting blood samples, a primed constant infusion of glucose is initiated. Plasma glucose levels are clamped at ~5 mmol/L by variable co-infusion of 20% glucose. Every 5 minutes, blood is sampled for immediate determination of plasma glucose concentration. Glucose infusion rate is adjusted to obtain plasma glucose levels of ~5 mmol/L (euglycemia). A bolus of insulin is then infused. Before and during steady state, substrate oxidation is measured using an indirect calorimeter, which determines metabolic flexibility.
Same as current
Complete list of historical versions of study NCT01298375 on ClinicalTrials.gov Archive Site
Evaluating mitochondrial function through measurement of phosphocreatine (PCr) recovery by phosphorus magnetic resonance spectroscopy (31P-MRS) within the skeletal muscle [ Time Frame: 1.5 hours ] [ Designated as safety issue: Yes ]
The quantification of energy metabolites (Pi, PCr and ATP) in skeletal muscle will be performed in the v. lateralis at rest, during submaximal knee-extension exercise and during recovery. The rate at which PCr concentration is restored after exercise is an excellent in vivo measure of skeletal muscle mitochondrial oxidative capacity.
Same as current
Not Provided
Not Provided
 
Metabolic Phenotyping in Humans
Metabolic Characterization of Type 2 Diabetic, Obese, Lean Sedentary and Endurance Trained Individuals in Vivo, ex Vivo and in Vitro

Type 2 diabetes (T2D) is a global burden disease affecting almost 200 million people and is expected to nearly double by 2030 (1). It is imperative that this disease is kept under control, and that we begin to reverse the direction of its incidence. We propose to start by identifying the physiological and molecular aspects of the problem in all spectrums of the disease (ie from insulin sensitive athletes to sedentary lean and obese individuals and further to overt type 2 diabetics), and focus our efforts on examining the differences and identifying the stages of progression for possible targets of future intervention. The proposed study "Metabolic Phenotyping" is novel in its target populations and innovative in its use of state-of-the-art techniques. We hypothesize that the in vivo differences in metabolic flexibility and mitochondrial function between endurance athletes and type 2 diabetics and their lean and obese controls are retained in vitro and will offer a new model in which to study the underlying mechanisms of the progression of T2D.

The aim of the present research proposal is to metabolically phenotype endurance trained athletes, lean and obese sedentary and type 2 diabetic individuals with the following objectives:

  1. assess metabolic flexibility as measured by a euglycemic-hyperinsulinemic clamp
  2. measure in vivo mitochondrial function by MRS of phosphocreatine (PCr) recovery
  3. establish primary myoblast cell lines to correlate with the above in vivo measurements, as well as further explore dietary, pharmacological and genetic manipulations in vitro
  4. quantify intramyocellular lipid (IMCL) and acetylcarnitine in vivo by MRS

Study population:

A total of 132 male participants (18-70 years) will participate in this study. The first group of 33 participants will be lean endurance-trained athletes, the second group will be lean sedentary control participants, the third group will be sedentary type 2 diabetic participants, and the last group of 33 participants will be obese, non-diabetic sedentary control participants. It is preferred to use male participants in order to minimize variation in the measurements by avoiding confounding factors such as hormones.

Main study parameters/endpoints: The main study parameters are differences in metabolic flexibility as measured by euglycemic-hyperinsulinemic clamp, PCr recovery, IMCL and acetylcarnitines as measured by MRS and establishment of primary myoblast cell lines for future use.

Observational
Observational Model: Cohort
Time Perspective: Cross-Sectional
Not Provided
Retention:   Samples With DNA
Description:

DNA, RNA, tissue, primary myoblasts, mitochondria

Non-Probability Sample

Human volunteers from the surrounding area

  • Healthy
  • Obesity
  • Type 2 Diabetes Mellitus
Not Provided
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
132
March 2013
March 2013   (final data collection date for primary outcome measure)

General Inclusion criteria:

  • Male sex
  • Generally healthy with specifically no known cardiovascular disease or gastric ulcers, which can affect the study parameters
  • Stable dietary habits (no weight loss/gain > 3 kg in the last 6 months)

Group 1, type 2 diabetes participants:

  • Ages 40-70 years
  • BMI > 30 kg/m2
  • Non-insulin dependent type 2 diabetes
  • Must be on sulphonylurea (SU)-derivate or metformin therapy for at least six months with a constant dose for at least two months, or on dietary treatment for at least six months
  • Well-controlled diabetes: HbA1c < 8%
  • No diabetes related co-morbidities like cardiovascular diseases, diabetic foot, polyneuropathy, retinopathy

Group 2, obese healthy control participants:

  • Ages 40-70 years
  • BMI > 30 kg/m2
  • A plasma glucose level lower than 6.1 mmol/L
  • No family history of diabetes
  • No medication use
  • Sedentary lifestyle; No participation in any physical activity for at least 2 years

Group 3, endurance trained athletes:

  • Ages 18-35 years
  • BMI < 25 kg/m2
  • No family history of diabetes
  • No medication use
  • VO2max > 55ml/kg/min
  • Active in competitive endurance-exercise activities, 3 times a week for at least 2 years
  • Stable level of training for at least 6 months

Group 4, lean healthy sedentary control participants:

  • Ages 18-35 years
  • BMI < 25 kg/m2
  • No family history of diabetes
  • No medication use
  • VO2max < 55ml/kg/min
  • Plasma glucose < 6.1 mmol/L
  • Sedentary lifestyle; No participation in physical activity for more than 1 hour per week for at least 2 years

General Exclusion criteria:

  • Regular smokers
  • Participation in other studies
  • Female sex
  • Insulin dependent diabetic individuals
  • Participants with diabetes related diseases (diabetic foot, diabetic polyneuropathy, diabetic retinopathy etc.)
  • Use of Thiazolidines (glitazone/rosiglitazone/pioglitazone/troglitazone)
  • Use of anti-coagulants (not thrombocyte-aggregation inhibitors)
  • Aberrant ECG (with signs of ischemia or cardiac failure or arrythmias)
  • Weight gain/loss > 3 kg in the last 6 months
  • HbA1c < 7.8 in type 2 diabetic individuals
  • Contraindications for MRS scans:

    • Electronic implants such as pacemakers or neurostimulator
    • Iron-containing foreign bodies in eyes or brain
    • Some hearing aids and artificial (heart) valves which are contraindicated for MRS
    • Claustrophobia
  • Participants, who do not want to be informed about unexpected medical findings, or do not wish that their physician be informed, cannot participate in the study.
Male
18 Years to 70 Years
Yes
Contact: Madeleen Bosma, M.S. 31433884254 m.bosma@maastrichtuniversity.nl
Contact: Bram Brouwers, B.S. 31433884258 b.brouwers@maastrichtuniversity.nl
Netherlands
 
NCT01298375
NL35178.068.11
Yes
Maastricht University Medical Center
Maastricht University Medical Center
Not Provided
Study Director: Patrick Schrauwen, PhD Maastricht University
Principal Investigator: Lauren M Sparks, PhD Maastricht University
Principal Investigator: Madeleen Bosma, M.S. Maastricht University
Maastricht University Medical Center
July 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP