Lactate and Glycerol Contribution to Gluconeogenesis

NCT ID: NCT06955130

Last Updated: 2025-12-02

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-07-01
• Study Completion Date: 2030-04-30

Brief Summary

A major cause of increased blood glucose levels in type 2 diabetes (T2D) is increased hepatic gluconeogenesis (GNG), as the liver converts various substrates into glucose. Two of these substrates include glycerol, a molecule from fat, and lactate, a molecule that circulates in the blood. Our previously collected data suggest that glycerol's role in this process has been underestimated, so the investigators will directly compare the carbon contribution of glycerol and lactate to new glucose production under fasting conditions in patients with and without T2D. The investigators will also assess how glucagon, a hormone that raises blood glucose levels, impacts the conversion of glycerol and lactate to glucose. Enrolled participants will undergo three separate isotope tracer infusions with serial blood collections for liquid chromatography-mass spectrometry analysis. This research could identify new therapeutic drug targets that can lower blood glucose levels more directly and effectively.

Detailed Description

Objectives:

1. Compare glycerol and lactate as carbon sources for GNG in humans with and without T2D.

2. Compare the contribution of glycerol and lactate to GNG during a hyperglucagonemic state.

Hypothesis:

1. Glycerol contributes to glucose and lactate production, while lactate is not a net carbon contributor to glucose or glycerol production.

2. Glycerol, not lactate, potentiates the observed increases in GNG seen in T2D.

3. Glucagon promotes greater glycerol incorporation into glucose as compared to lactate incorporation into glucose.

Study Design:

The investigators will recruit three different adult metabolic cohorts (16 per cohort): 1) Lean, defined as body mass index (BMI) <25.0 kg/m2, and no T2D; 2) Obese (BMI ≥ 30.0 kg/m2) and no T2D; and 3) Obese (BMI ≥ 30.0 kg/m2) and with T2D. All subjects will be between the ages of 18 and 65. All subjects will perform a self-monitored overnight fast at home and then come for three separate isotope tracer infusions (13C3-glycerol, 13C3-lactate, and 13C6-glucose) with serial blood draws. Each tracer infusion will last eight hours. During the final two hours of the infusion, subjects will receive intravenous glucagon, which increases the amount of glucose the liver produces. Collected blood samples will undergo liquid chromatography-mass spectrometry (LC-MS) analysis in our laboratory. Additionally, all subjects will receive a body composition analysis via dual-energy X-ray absorptiometry (DXA).

Conditions

Type 2 Diabetes; Obesity; Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Glycerol

Each subject will receive labeled 13C3-glycerol.

Group Type: EXPERIMENTAL

Glycerol

Intervention Type: DRUG

Subjects will receive an infusion of glycerol and glucagon.

Lactate

Each subject will receive labeled 13C3-lactate.

Group Type: EXPERIMENTAL

Lactate

Intervention Type: DRUG

Subjects will receive an infusion of lactate and glucagon.

Glucose

Each subject will receive labeled 13C6-glucose.

Group Type: EXPERIMENTAL

Glucose

Intervention Type: DRUG

Subjects will receive an infusion of glucose and glucagon.

Interventions

Glycerol

Subjects will receive an infusion of glycerol and glucagon.

Intervention Type: DRUG

Lactate

Subjects will receive an infusion of lactate and glucagon.

Intervention Type: DRUG

Glucose

Subjects will receive an infusion of glucose and glucagon.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age 40-70 years.

2. The subject is otherwise in general good health, based on medical history and physical examination.

1. No evidence of T2D or prediabetes as indicated by the American Diabetes Association (ADA), i.e., HbA1c < 5.7%, fasting glucose < 100 mg/dL, or use of glucose-lowering medications.

2. Body mass index (BMI) ≤ 24.9 kg/m2.

1. No evidence of T2D or prediabetes as per ADA criteria.

2. 30.0 ≤ BMI ≤ 45.0 kg/m2.

1. Evidence of T2D as indicated by ADA criteria.

2. 6.5% ≤ HbA1c ≤ 8.0%.

3. 30.0 ≤ BMI ≤ 45.0 kg/m2.

Exclusion Criteria

1. Chronic medical conditions that may affect glucose metabolism, including active malignancy, tobacco use, HIV infection, kidney failure, liver dysfunction, alcoholism, pancreatitis, active viral/bacterial infection, current pregnancy/lactation, anemia, severe cardiac or respiratory failure, and uncontrolled hyperlipidemia (total cholesterol ≥ 260 mg/dL or triglycerides ≥400 mg/dL).

2. Current medical therapy that affects glucose metabolism such as glucocorticoid, antipsychotic, or oral contraceptive pills.

3. Type 1 diabetes mellitus diagnosis and/or history of diabetic ketoacidosis.

4. Use of weekly glucagon-like peptide-1 (GLP-1) receptor agonist therapy.

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Rutgers, The State University of New Jersey

OTHER

Sponsor Role: lead

Responsible Party

Ankit Shah, MD

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ankit Shah, MD

Role: PRINCIPAL_INVESTIGATOR

Rutgers Robert Wood Johnson Medical School

Central Contacts

Ankit Shah, MD

Role: CONTACT

ashah386@rwjms.rutgers.edu

7322356337

Other Identifiers

Pro2019002628

Identifier Type: -

Identifier Source: org_study_id