Effect of Insulin Resistance on Branched Chain Amino Acid Metabolism. (BCAA)
Obesity, Insulin Resistance
About this trial
This is an interventional basic science trial for Obesity
Eligibility Criteria
Inclusion Criteria:
Inclusion criteria for cases (subjects with insulin resistance).
- Male and female.
- Adults between 18 and 50 years of age.
- Body Mass Index (BMI) ≥ 18.5 and ≤ 40 kg/m2.
- HOMA index ≥ 2.5
- In the case of women, being in the follicular phase of the menstrual cycle.
Inclusion criteria for controls (subjects without insulin resistance).
- Male and female
- Adults between 18 and 50 years of age.
- Body Mass Index (BMI) ≥ 18.5 and ≤ 40 kg/m2.
- HOMA index < 2.5
- Blood glucose < 100 mg/dL
- In the case of women, being in the follicular phase of the menstrual cycle.
Exclusion Criteria:
- Patients with any type of diabetes.
- Patients with kidney disease diagnosed by any physician.
- Patients with creatinine > 1.3 mg/dL for men and > 1.1 mg/dL for women and/or Blood Urea Nitrogen (BUN) > 20 mg/dL.
- Patients with acquired diseases secondarily producing obesity and diabetes.
- Patients who have suffered a cardiovascular event.
- Weight loss > 3 kg in the last 3 months.
- Patients with any catabolic diseases.
- Pregnancy status.
- Positive smoking.
- Treatment with any medication (except contraceptives and proton pump inhibitors)
- Having suffered any infection in the last 20 days.
Sites / Locations
- Instituto Nacional de Ciencias Medicas Y Nutricion Salvador Zubiran
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Subjects with a Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) ≥ 2.5
Subjects with a Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) < 2.5
Administration of an 8% crystalline L-amino acid solution with high concentrations of branched chain amino acids. The dose will be calculated considering the 25% of the estimated protein per day (1 g/kg/day). This dose will be placed in a short peripheral intravenous catheter and administered at a rate of 1.5ml per minute, using an infusion pump. The patient will be monitored all the time by a physician.
Administration of an 8% crystalline L-amino acid solution with high concentrations of branched chain amino acids. The dose will be calculated considering the 25% of the estimated protein per day (1 g/kg/day). This dose will be placed in a short peripheral intravenous catheter and administered at a rate of 1.5ml per minute, using an infusion pump. The patient will be monitored all the time by a physician.