MedPath

Evaluating Glial Acetate Metabolism as a Biomarker of Hypoglycemic Counterregulation

Not Applicable
Recruiting
Conditions
Diabetes
Hypoglycemia
Interventions
Other: hyperinsulinemic-hypoglycemic clamp
Other: 13C-MRS procedure/Acetate infusion
Registration Number
NCT04207619
Lead Sponsor
Pennington Biomedical Research Center
Brief Summary

Hypoglycemic complications are a major impediment to the maintenance of healthy glucose levels in persons with diabetes. The investigators recently completed a clinical pilot and feasibility study (GLIMPSE, NCT02690168), which identified a novel biomarker, glial acetate metabolism, that appears to predict the susceptibility to hypoglycemia. By providing an assay to predict hypoglycemic events and therefore diabetic complications, the development of this biomarker could significantly improve the treatment of persons with diabetes.

The goal of this study is to determine the efficacy of our biomarker for predicting susceptibility to insulin-induced hypoglycemia. In order to accomplish this goal the investigatiors will pair our 13C magnetic resonance spectroscopy procedure to assess glial acetate metabolism, developed in the GLIMPSE study, with a hyperinsulinemic-hypoglycemic clamp procedure, developed in the HYPOCLAMP study (NCT03839511). The two procedures will be separated by a three day interval. The investigators will then correlate the participants' rates of glial acetate metabolism with their neuroendocrine responses to the hypoglycemic clamp. This proof of concept study will test the hypothesis that glial acetate metabolism is inversely proportional to the neuroendocrine response to hypoglycemia, that is, as glial acetate metabolism increases the neuroendocrine response will decrease.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
10
Inclusion Criteria
  • Healthy male or female
  • Ages 18-40 years
  • BMI between 20 kg/m2 and 30 kg/m2 (±0.5 kg/m2 will be accepted)
  • Medically cleared for participation in the study
Exclusion Criteria
  • Contraindication to MRI
  • Consume >10 alcoholic drinks/week
  • History of chronic smoking or have quit less than 10 years ago
  • History of clinically diagnosed diabetes or a fasting blood glucose >126 mg/dL
  • Average screening blood pressure >140/90 mmHg
  • History of cardiovascular disease
  • Pregnant, planning to become pregnant, or breastfeeding
  • Use of medications affecting glucose metabolism, e.g., benzodiazepines, thiazide diuretics, cortisone, and prednisone.
  • Use of beta-adrenergic antagonists.
  • Based on the investigative team's clinical judgement, a subject may not be appropriate for participation in the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Arm 1hyperinsulinemic-hypoglycemic clampParticipants will have their glial acetate metabolism measured by carbon-13 magnetic resonance spectroscopy as well as their neuroendocrine response to hypoglycemia 3 days later.
Arm 113C-MRS procedure/Acetate infusionParticipants will have their glial acetate metabolism measured by carbon-13 magnetic resonance spectroscopy as well as their neuroendocrine response to hypoglycemia 3 days later.
Primary Outcome Measures
NameTimeMethod
Percent 13C enrichment of bicarbonate measured via carbon-13 magnetic resonance spectroscopy (13C-MRS)Every ten minutes for 120 minutes following administration of 1-13C acetate

Glial acetate metabolism

Secondary Outcome Measures
NameTimeMethod
Change in serum epinephrine levelsepinephrine will be measured every 15 minutes for 135 minutes.

The change is serum epinephrine during the hypoglycemic clamp will be determined relative to baseline levels

Trial Locations

Locations (1)

Pennington Biomedical Research Center

🇺🇸

Baton Rouge, Louisiana, United States

© Copyright 2025. All Rights Reserved by MedPath