The Effects of Glucagon on Hepatic Metabolism in People With Type 2 Diabetes After Caloric Restriction

Sponsor
Adrian Vella (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05499702
Collaborator
(none)
20
1
1
28
0.7

Study Details

Study Description

Brief Summary

Caloric restriction (and RYGB) improves insulin action and lowers fasting glucose, glucagon and EGP, without changes in postprandial EGP and glucagon concentrations. Caloric restriction also improves hepatic steatosis and lowers fasting AA. These changes may represent restoration of glucagon's hepatic actions. This experiment will determine whether caloric restriction improves glucagon's actions on hepatic amino acid, carbohydrate and lipid metabolism in T2DM in comparison to a baseline experiment performed separately in people with T2DM.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Caloric Restriction
  • Drug: Hyperglycemic clamp
Phase 2

Detailed Description

T2DM and prediabetes are characterized by abnormal post-prandial suppression of glucagon, which contributes to postprandial hyperglycemia by increasing EGP. Although these effects are magnified by decreased and delayed insulin secretion, they are also apparent when insulin secretion is intact5. In rodents, altered glucagon signaling changes α-cell function and mass

  • an effect mediated by changes in circulating AA concentrations. Are the elevated concentrations of branched-chain AA and other AA metabolites in T2DM a cause or an effect of global α-cell dysfunction? Could altered glucagon signaling precipitate a vicious cycle resulting in T2DM?

This study will determine how caloric restriction alters hepatic glucagon action. Elevated fasting AA concentrations are associated with T2DM risk. In addition, hepatic steatosis has been associated with an impaired ability of glucagon to stimulate hepatic clearance of AAs. Prior studies have shown that caloric restriction lowers fasting glucose, EGP and glucagon. However, the effects on these parameters in the postprandial period are unclear. This experiment will examine to what degree the improvements produced by caloric restriction can be explained by improved hepatic glucagon action. Because caloric restriction decreases hepatic fat content the experiment will also determine if a reduction in hepatic fat content is associated with changes in glucagon's effects on hepatic AA, glucose, and lipid metabolism.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
caloric restriction for six weekscaloric restriction for six weeks
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
The Effects of Glucagon on Hepatic Metabolism in People With Type 2 Diabetes After Caloric Restriction
Anticipated Study Start Date :
Dec 1, 2022
Anticipated Primary Completion Date :
Dec 30, 2024
Anticipated Study Completion Date :
Mar 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Adults with type 2 diabetes

20 subjects will be studied on one occasion, following 6 weeks of caloric restriction. They will be instructed to consume a diet of 900 kcal daily using meals derived from "Nutritional Guidelines after Bariatric Surgery". Compliance will be monitored by weekly meetings with the dietician using an electronic record of food intake. After this subjects will undergo a hyperglycemic clamp with 2 doses of glucagon infused.

Behavioral: Caloric Restriction
Subjects will be instructed to consume a diet of 900 kcal daily using meals derived from "Nutritional Guidelines after Bariatric Surgery". Compliance will be monitored by weekly meetings with the dietician using an electronic record of food intake

Drug: Hyperglycemic clamp
Hyperglycemic clamp to measure the effect of glucagon on hepatic metabolism

Outcome Measures

Primary Outcome Measures

  1. Rate of leucine oxidation in response to rising glucagon concentrations [240 minutes of study]

    tracer-determined amino acid catabolism

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • We will recruit up to 20 weight-stable, subjects with type 2 diabetes

  • BMI ≥ 28 Kg/M2

  • Diabetes is managed by diet alone or a combination of oral agents

Exclusion Criteria:
  • History of prior upper abdominal surgery e.g. gastric banding, pyloroplasty, vagotomy.

  • Active systemic illness or malignancy.

  • Symptomatic macrovascular or microvascular disease.

  • Contraindications to MRI (e.g. metal implants, claustrophobia).

  • Hematocrit < 35%

  • TSH < 0.4 or > 5.5.

  • Consumption of > 2 alcohol drinks per day or > 14 per week or a positive AUDIT questionnaire.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic in Rochester Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Adrian Vella

Investigators

  • Principal Investigator: Adrian Vella, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Adrian Vella, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT05499702
Other Study ID Numbers:
  • 22-000233
First Posted:
Aug 12, 2022
Last Update Posted:
Aug 12, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Adrian Vella, Principal Investigator, Mayo Clinic
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 12, 2022