Micro Glucagon During Exercise in Type 1 Diabetes
Study Details
Study Description
Brief Summary
This proof-of-principle study to assess effects of different doses (mini and micro) of subcutaneous glucagon analog Dasiglucagon (Zealand Pharma, Copenhagen, Denmark) on the change in blood glucose concentration during moderate-intensity exercise in people with T1D.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Early Phase 1 |
Detailed Description
People with type 1 diabetes (T1D) are recommended to engage in regular exercise for a variety of health and fitness reasons. However, moderate-intensity exercise is associated with an increased risk of hypoglycaemia in people with T1D. Current guidelines are to reduce insulin dose and/or increase carbohydrate consumption in the context of the exercise bout. However, despite the many advances in insulin formulations and delivery devices, hypoglycaemia remains a significant risk. Mini-dose glucagon taken before an exercise bout has been shown to be an effective non-caloric strategy to prevent exercise-induced hypoglycaemia. However, even the reduced doses (150-200 µg) used in previous studies might still be rather high translating into potential side-effects (i.e. hyperglycaemia, gastrointestinal symptoms, etc.). Lower doses (below 100 µg, micro-glucagon) may be sufficiently effective to counteract hypoglycaemia risk associated with exercise and associated with better tolerance. Moreover, there is little information on the effects of subcutaneous glucagon on glycogen stores and changes in exercise metabolism. Greater understanding of exercise-associated metabolism following mini- and micro-dose glucagon using techniques such as magnetic resonance spectroscopy (MRS), continuous glucose monitoring (CGM), stable isotope tracers, and indirect calorimetry may result in novel approaches to improve blood glucose management in people with T1D. Utilising these techniques may also further our understanding of the optimal glucagon dosing (timing and amount) during exercise to manage hypoglycaemia and reduce the risk of adverse events. Proof-of-principle study to assess effects of different doses (mini and micro) of subcutaneous glucagon analog Dasiglucagon (Zealand Pharma, Copenhagen, Denmark) on the change in blood glucose concentration during moderate-intensity exercise in people with T1D. Secondly, to investigate exercise-metabolism following Dasiglucagon injection using 3 tesla magnetic resonance spectroscopy (MRS) and indirect calorimetry. Third, to assess participant experience of Dasiglucagon during exercise and the incidence of adverse events.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Micro-dose glucagon 80 µg (micro-dose) subcutaneous Dasiglucagon 5 min before the start of exercise |
Drug: Micro-glucagon
Administration of 80 µg (micro-dose) subcutaneous Dasiglucagon 5 min before the start of exercise
Other Names:
|
| Experimental: Mini-dose glucagon 150 µg mini-dose of subcutaneous Dasiglucagon 5 min before exercise the start of exercise |
Drug: Mini-glucagon
Administration of 150 µg (mini-dose) subcutaneous Dasiglucagon 5 min before the start of exercise
Other Names:
|
| No Intervention: No treatment No treatment before the start of exercise |
Outcome Measures
Primary Outcome Measures
- Time to hypoglycaemia [60 minutes]
Time (in minutes) to hypoglycaemia (plasma glucose <3.9mmol/l) during 60 minutes of aerobic exercise in individuals with type 1 diabetes using mini and micro doses of Dasiglucagon compared to no Dasiglucagon
Secondary Outcome Measures
- Change in glycaemia during exercise [60 minutes]
Change in blood glucose concentration, calculated based on the participants' glucose at the start of exercise and the last value measured at the end of exercise. If the exercise is stopped early because of hypoglycaemia, the last exercise glucose value will be used for analysis
- Glucose during exercise [60 minutes]
Mean glucose concentration and area under the glucose curve during exercise
- Glucagon during exercise [60 minutes]
Mean glucagon concentration and area under the glucagon curve during exercise
- Time in target [24 hours]
Time in target glycaemic range (4-10 mmol/L) in the recovery period and overnight
- Time in target during exercise [60 minutes]
Time in target glycaemic range (4-10 mmol/L) during exercise
- Hypoglycaemia [24 hours]
Incidence of hypoglycaemia (≤3.9 mmol/L for 15 min or more) during the 24 hour post exercise recovery period
- Glycogen content [4 hours]
Change in skeletal muscle and hepatic glycogen following exercise
- Any adverse events [24 hours]
Adverse symptoms following glucagon/placebo use
Eligibility Criteria
Criteria
Inclusion Criteria:
-
T1D for >1 year
-
Male aged 18-45 years old
-
HbA1c <8.0% (64 mmol/mol) based on analysis from the central laboratory unit of Bern University Hospital
-
Regular physical activity (defined as meeting 150 min moderate-intensity exercise per week)
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Using either continuous subcutaneous insulin infusion or multiple daily injections
-
Written informed consent
Exclusion Criteria:
-
Physical or psychological disease likely to interfere with the normal conduct of the study and interpretation of the results as judged by the investigator
-
Current treatment with drugs known to interfere with metabolism e.g. systemic corticosteroids, statins, SGLT2 inhibitors, GLP1 agonists
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Relevant diabetic complications as judged by the investigator
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Body mass index 30 kg/m2
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Uncontrolled hypertension (>180/100 mmHg)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital and University of Bern, Bern, Switzerland | Bern | Switzerland | 3010 |
Sponsors and Collaborators
- University Hospital Inselspital, Berne
Investigators
- Principal Investigator: Christoph Stettler, MD, Clinic Director
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- GLU-01