Role of BCAA in Glucose Homeostasis

Phase 4

Not yet recruiting

• Conditions: Type 2 Diabetes
• Interventions: Drug: 4.8 g/m^2/day placebo; Drug: 4.8 g/m^2/day NaPB

• Registration Number: NCT05836350
• Lead Sponsor: Maastricht University

Brief Summary

This clinical trial study aims to evaluate the effects of prolonged NaPB treatment in a maximum of 20 patients with T2D. The primary objective is:

to investigate if prolonged boosting of ing BCAA oxidation will substantially lower plasma glucose levels in patients with T2D.

Participants will undergo a Clinical randomized controlled trial (RCT) with a double-blinded, placebo-controlled, cross-over design, including a wash-out period of 12 weeks. The trial will contain 2 treatment arms, with each a duration of 12 weeks.

Participants will have a 12-week oral administration of 4.8 g/m2/day NaPB (in the form of Pheburane) or placebo per day. Although depending on body surface area, \~21 g Pheburane needs to be administered spread over the day 3 times taken with a meal.

Detailed Description

Several studies identified branched-chain amino acids (BCAA; leucine, isoleucine, and valine) to be substantially elevated in people with T2D, possibly caused by lower BCAA oxidation rates. Plasma BCAA levels are strongly associated with insulin resistance and other key metabolic disarrangements as seen in T2D, including mitochondrial function, liver fat content, and metabolic flexibility. We, recently, showed that stimulating BCAA oxidation for 2 weeks with sodium-phenylbutyrate (NaPB) treatment -a drug known to accelerate BCAA oxidation- decreased BCAA plasma levels in patients with T2D. This reduction in plasma BCAA levels was paralleled with a robust improvement in peripheral insulin sensitivity and muscle mitochondrial oxidative capacity. Interestingly, a strong tendency was found for lower fasting glucose levels, an indication of better glucose control. These findings form lead to further evaluating this treatment strategy to improve glucose homeostasis and lower hyperglycaemic conditions in patients with T2D. So far, this strategy has been tested only in several rodent models reporting promising, beneficial outcomes on glucose homeostasis and heart function.

The aim of the present study is to evaluate the effects of prolonged treatment: patients with T2D will undergo a 12-week NaPB intervention with the aim of substantially lower fasting plasma glucose levels. The outcomes of this project evaluate a novel strategy to treat patients with T2D.

Study Timeline

• Status Verified: 2023-04
• Study First Submitted: 2023-04-07
• Study First Submitted QC: 2023-04-26
• Last Update Submitted: 2023-04-26
• Study First Posted: 2023-05-01
• Last Update Posted: 2023-05-01
• Study Start: 2023-06
• Primary Completion: 2025-10
• Study Completion: 2026-05

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Patients are able to provide signed and dated written informed consent prior to any study specific procedures
2. Women are post-menopausal (defined as at least 1 year post cessation of menses) and aged ≥ 45 and ≤ 76 years. Males are aged ≥ 40 years and ≤ 76 years
3. Patients should have suitable veins for cannulation or repeated venipuncture
4. Caucasians
5. BMI: 25-38 kg/m2
6. Diagnosed with T2D at least 1.5 years before the start of the study
7. Relatively well-controlled T2D: HbA1c < 8.5%
8. Oral glucose lowering medication: metformin only or in combination with sulfonylurea agents and/or on stable dose of a DPPIV inhibitor treatment for at least the last 3 months
9. No signs of active diabetes-related co-morbidities like active cardiovascular diseases, active diabetic foot, polyneuropathy or retinopathy
10. No signs of active liver or kidney malfunction

Exclusion Criteria

1. Previous enrolment in a clinical study with an investigational product during the last 3 months or as judged by the Investigator

2. Participate in physical activity more than 3 times a week

3. Unstable body weight (weight gain or loss > 5 kg in the last three months)

4. Insulin dependent T2D

5. Patients with congestive heart failure and and/or severe renal and or liver insufficiency or known sodium retention with oedema

6. Patients using Probalan (probenecid), Haldol (haloperidol), Depakene (valproate) or medical products containing corticosteroids

7. Men: Hb <8.4 mmol/L, Women: Hb <7.8 mmol/l

8. Any contra-indication MRI scanning. These contra-indications include patients with e.g. the following:

   • Central nervous system aneurysm clip
   • Implanted neural stimulator
   • Implanted cardiac pacemaker of defibrillator
   • Cochlear implant
   • Metal containing corpora aliena in the eye or brains

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
4.8 g/m^2/day Placebo	4.8 g/m^2/day placebo	12-week oral administration of 4.8 g/m2/day identical placebo granules.
4.8 g/m^2/day NaPB	4.8 g/m^2/day NaPB	12-week oral administration of 4.8 g/m\^2/day Sodium-phenylbutyrate (NaPB) (in the form of Pheburane)

Primary Outcome Measures

Name	Time	Method
fasting plasma glucose levels	at week 12 of each intervention period	Glucose levels will be measured after an overnight fast expressed in mmol/l.

Secondary Outcome Measures

Name	Time	Method
cardiac function: peak A-wave velocity (cm/sec)	at week 12 of each arm	The cardiac function will be measured via diastolic cardiac function with the use of ultrasound (transthoracic echocardiography) with the following parameter: Peak A-wave velocity (cm/sec)
whole-body insulin sensitivity	at week 6 and week 12 of each intervention period	glucose clearance in ml/kg determined during an OGTT at 6 weeks glucose disposal rate (delta Rd) in umol/kg/min measured with the clamp at 12 weeks
muscle mitochondrial function	at week 6 and week 12 of each intervention period	O2-flux will be measured with high-resolution respirometry
cardiac function: pulsed wave TDI velocity (cm/sec) at lateral and septal basal regions	at week 12 of each arm	The cardiac function will be measured via diastolic cardiac function with the use of ultrasound (transthoracic echocardiography) with the following parameter: Pulsed wave TDI velocity (cm/sec) at lateral and septal basal regions
whole-body metabolic flexibility	at week 12 of each intervention period	insulin-stimulated change in respiratory exchange ratio will be determined with use of indirect calorimetry during the clamp
energy status of the heart	at week 12 of each arm	PCr/ATP-ratio will be determined with phosphorus magnetic resonance spectroscopy
cardiac function: left atrial maximum volume	at week 12 of each arm	The cardiac function will be measured via diastolic cardiac function with the use of ultrasound (transthoracic echocardiography) with the following parameter: Left atrial maximum volume (ml)
cardiac function: ejection fraction	at week 12 of each arm	The cardiac function will be measured via ejection fraction (microL) with the use of cine-MRI
cardiac function: tricuspid regurgitation systolic jet velocity	at week 12 of each arm	The cardiac function will be measured via diastolic cardiac function with the use of ultrasound (transthoracic echocardiography) with the following parameter: Tricuspid regurgitation systolic jet velocity (m/sec)
cardiac function: peak E-wave velocity	at week 12 of each arm	The cardiac function will be measured via diastolic cardiac function with the use of of ultrasound (transthoracic echocardiography) will be assessed with the following parameters: Peak E-wave velocity (cm/sec)