Obesity-Related Glycine Deficiency: Investigating a Long-standing Metabolic Paradox Using Bedside and Bench Approaches

Completed

• Conditions: Insulin Resistance; Oxidative Stress; Glycine Metabolism Disturbances; Morbid Obesity
• Interventions: Procedure: Bariatric surgery

• Registration Number: NCT04660513
• Lead Sponsor: Singapore General Hospital

Brief Summary

Obesity, in addition to causing abnormal glucose and lipid metabolism, is also associated with altered plasma concentrations of multiple amino acids, including increased levels of branched-chain amino acids and decreased levels of glycine. The mechanisms and consequences of obesity- related glycine deficiency are unknown.

The overall aim of this project is to comprehensively study glycine metabolic pathways in morbid obesity using stable-isotope tracer techniques in human subjects and validating kinetic findings using a cell model of oxidative stress.

This will be a single-centre, observational study. 21 individuals with morbid obesity scheduled for bariatric surgery and 21 non-obese controls will be recruit. They will undergo different study visits and procedures and the human biological materials collected will be analysed for as per aims of the studies. We believe that the glycine metabolic pathways, possibly through the optimization of gluthathione (GSH) synthesis, may provide targets to develop novel therapeutic agents.

Detailed Description

Metabolic tracers: 1,2-\[13C2\]-Glycine, 1,2-\[13C2\]-Glycine, 2,3,3,-\[2H3\]-Serine and \[2H5\]-Phenylalanine will be infused for quantification of various pathways associated with glycine metabolism.

Study Timeline

• Study Start: 2018-12-08
• Primary Completion: 2020-11-04
• Study Completion: 2020-11-04
• Status Verified: 2020-12
• Study First Submitted: 2020-12-01
• Study First Submitted QC: 2020-12-07
• Last Update Submitted: 2020-12-07
• Study First Posted: 2020-12-09
• Last Update Posted: 2020-12-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

1. Age: 21-65 years
2. BMI < 25 kg/m2 for non-obese controls or BMI ≥ 32.5 kg/m2 for obese subjects scheduled for bariatric surgery
3. Able to provide informed consent

Exclusion Criteria

All subjects:

1. Weight > 150 kg
2. Renal impairment (estimated creatinine clearance estimated by Cockcroft-Gault Equation < 60 ml/min)
3. Haemoglobin concentration < 10 g/L
4. Serum alanine aminotransferase or aspartate aminotransferase above 2x upper limit of normal
5. Uncontrolled hypertension (BP > 180/110 mmHg)
6. Pregnancy
7. Nursing mothers
8. Significant cardiovascular disease (e.g. acute myocardial infarction, congestive cardiac failure, ischemic heart disease, atrial fibrillation, sick sinus syndrome, supraventricular tachycardia)
9. Previous stroke
10. Uncontrolled thyroid disease
11. Surgery requiring general anaesthesia within 4-weeks before enrolment
12. Psychiatric disorders requiring medication
13. Significant alcohol intake (> 1 unit per day for women and > 2 units per day for men)
14. Subcutaneous insulin injections
15. Systemic steroid usage (eg. prednisolone, hydrocortisone, cortisone, dexamethasone)
16. Cancer within the last 5-years (except squamous cell and basal cell cancer of the skin)
17. Any factors likely to limit adherence to study protocol (e.g. dementia; alcohol or substance abuse; history of unreliability in medication taking or appointment keeping; significant concerns about participation in the study from spouse, significant other or family members)

Non-obese controls 1. Known Diabetes Mellitus (diagnosed according to 2014 Ministry of Health Clinical Practice Guidelines for Diabetes Mellitus)

Obese subjects

1. HbA1C < 9%

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Morbid obesity	Bariatric surgery	BMI 32.5 kg/m2 and above

Primary Outcome Measures

Name	Time	Method
Glycine kinetic	Baseline for all subjects and 5-12 months after bariatric surgery for morbid obesity group	Differences in glycine kinetic measurements between obese subjects and controls, and within obese subjects after bariatric surgery
Insulin sensitivity	Baseline for all subjects and 5-12 months after bariatric surgery for morbid obesity group	Differences in insulin sensitivity between obese subjects and controls, and within obese subjects after bariatric surgery

Trial Locations

Locations (1)

Singapore General Hospital; 🇸🇬 Singapore, Singapore