L-arginine and Brown Adipose Tissue (ArgMB)
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|ClinicalTrials.gov Identifier: NCT02291458|
Recruitment Status : Unknown
Verified November 2014 by Maastricht University Medical Center.
Recruitment status was: Recruiting
First Posted : November 14, 2014
Last Update Posted : November 14, 2014
|Condition or disease||Intervention/treatment||Phase|
|Adipose Tissue, Brown Glucose Intolerance Nitric Oxide||Drug: L-arginine Drug: Placebo||Phase 3|
Rationale: The South Asian population originally descends from the Indian subcontinent and represents approximately 20% of the total world population. This population is facing an epidemic of type 2 diabetes, of which the underlying cause is still unknown. A high prevalence of a disadvantageous metabolic phenotype, consisting of obesity, insulin resistance and dyslipidemia, may at least in part contribute to this excess risk. It is currently hypothesized that an ethnic susceptibility towards a disturbed energy metabolism may underlie this disadvantageous metabolic phenotype. In line with this, the investigators recently discovered that Dutch South Asian subjects have 32% lower resting energy expenditure (REE) and 34% lower energy-combusting brown adipose tissue (BAT) compared to matched white Caucasians. Nitric oxide (NO) was recently shown to be crucial for BAT development and, interestingly, South Asians have diminished NO bioavailability. Thus, the disadvantageous metabolic phenotype in South Asians may be caused by diminished NO bioavailability resulting in lower BAT volume. Therefore, the investigators hypothesize that increasing NO generation in the body by administration of L-arginine, the precursor of NO, will improve their metabolic phenotype by increasing BAT volume, thereby increasing REE and clearance of triglycerides and glucose by BAT.
Objectives: The primary objectives are: 1) to determine the effect of L-arginine on glucose uptake by brown adipose tissue and to assess whether the effect differs between South Asian and white Caucasian subjects; 2) to determine the effect of L-arginine on whole body energy expenditure and to assess whether the effect differs between South Asian and white Caucasian subjects; 3) to determine the effect of L-arginine on fat mass and to assess whether the effect differs between South Asian and white Caucasian subjects.
Study design: A randomized placebo-controlled multicenter cross-over study will be performed in moderately obese Dutch South Asians and matched white Caucasians. Subjects will receive L-arginine (9 gram/day) or placebo for 6 weeks, followed by a wash-out period of 4 weeks and then again 6 weeks of one of either treatments. At the end of both treatment periods, a cold-induced PET-CT scan will be performed. Furthermore, muscle and fat biopsies will be obtained, thermoregulation will be assessed, an oral glucose tolerance will be performed and the investigators will assess NO-dependent and independent vasodilation by means of iontophoresis.
Study population: Mildly obese (BMI 25-30 kg/m2) pre-diabetic male volunteers of South Asian and white Caucasian descent aged between 35-50 years.
Intervention: The intervention will consist of administration of 9 grams of L-arginine per day in three gifts (3dd 3 gram).
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||26 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||The Effect of L-arginine on Brown Adipose Tissue Metabolism in South Asian and White Caucasian Subjects|
|Study Start Date :||November 2014|
|Estimated Primary Completion Date :||October 2015|
|Estimated Study Completion Date :||December 2015|
Subjects will receive 9 gram of L-arginine per day in three gifts (3dd 3 gram) during 6 weeks.
9 gram L-arginine / day for 6 weeks
Other Name: Argimax
Placebo Comparator: Placebo
Subjects will receive 9 gram of placebo per day in three gifts (3 dd 3 gram) during 6 weeks.
9 gram placebo / day for 6 weeks
- Standard uptake value of Brown adipose tissue [ Time Frame: 6 weeks ]Glucose uptake by brown adiopse tissue will be assessed by cold-induced 18F-FDG PET-CT scan
- Energy expenditure [ Time Frame: 6 weeks ]Energy expenditure will be determined by means of indirect calorimetrie
- Fat mass [ Time Frame: 6 weeks ]Fat mass will be determined by DEXA scan
- Body temperatures [ Time Frame: 6 weeks ]Skin and core body temperatures as well as gradients will be assessed by means of iButtons and ingestion of a telemetric pill, respectively.
- Skin perfusion and endothelial-dependent and independent vasodilation [ Time Frame: 6 weeks ]This will be measured by means of Laser Doppler Flowmetry (LDF) and iontophoresis
- Skeletal muscle mitochondrial respiration/uncoupling [ Time Frame: 6 weeks ]This will be determined in muscle biopsies by using the Oroboros 2k Oxygraph instrument present in our laboratory .
- Brown adipocyte recruitment and inflammation in WAT [ Time Frame: 6 weeks ]This will be measured in subcutaneous WAT biopsies by assessing mRNA expression via real time polymerase-chain reaction (RT-PCR) and protein content by immunohistochemical stainings.
- Blood parameters [ Time Frame: 6 weeks ]Venous blood will be drawn by means of a catheter placed in the antecubital vein of the underarm. By using radioimmunoassay, high performance liquid chromotogaphy (HPLC) and enzyme-linked immunosorbent assay (ELISA), blood parameters (i.e. lipids, glucose, inflammatory markers and endothelial activation markers) will be analyzed. In addition, we will perform DNA analyses from blood.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02291458
|Maastricht University Medical Center +||Recruiting|
|Maastricht, Limburg, Netherlands, 6229 ER|
|Contact: Mariette Boon, PhD +31648126425 firstname.lastname@example.org|
|Contact: Wouter van Marken Lichtenbelt, PhD Tel: +31 43 388 1629 email@example.com|