TY - JOUR
T1 - Metabolic effect of adrenaline infusion in people with type 1 diabetes and healthy individuals
AU - She, Rui
AU - Suvitaival, Tommi
AU - Andersen, Henrik U
AU - Hommel, Eva
AU - Nørgaard, Kirsten
AU - Wojtaszewski, Jørgen F P
AU - Legido-Quigley, Cristina
AU - Pedersen-Bjergaard, Ulrik
N1 - © 2024. The Author(s).
PY - 2024/6
Y1 - 2024/6
N2 - AIMS/HYPOTHESIS: As a result of early loss of the glucagon response, adrenaline is the primary counter-regulatory hormone in type 1 diabetes. Diminished adrenaline responses to hypoglycaemia due to counter-regulatory failure are common in type 1 diabetes, and are probably induced by exposure to recurrent hypoglycaemia, however, the metabolic effects of adrenaline have received less research attention, and also there is conflicting evidence regarding adrenaline sensitivity in type 1 diabetes. Thus, we aimed to investigate the metabolic response to adrenaline and explore whether it is modified by prior exposure to hypoglycaemia.METHODS: Eighteen participants with type 1 diabetes and nine healthy participants underwent a three-step ascending adrenaline infusion during a hyperinsulinaemic-euglycaemic clamp. Continuous glucose monitoring data obtained during the week before the study day were used to assess the extent of hypoglycaemia exposure.RESULTS: While glucose responses during the clamp were similar between people with type 1 diabetes and healthy participants, plasma concentrations of NEFAs and glycerol only increased in the group with type 1 diabetes (p<0.001). Metabolomics revealed an increase in the most common NEFAs (p<0.01). Other metabolic responses were generally similar between participants with type 1 diabetes and healthy participants. Exposure to hypoglycaemia was negatively associated with the NEFA response; however, this was not statistically significant.CONCLUSIONS/INTERPRETATION: In conclusion, individuals with type 1 diabetes respond with increased lipolysis to adrenaline compared with healthy participants by mobilising the abundant NEFAs in plasma, whereas other metabolic responses were similar. This may suggest that the metabolic sensitivity to adrenaline is altered in a pathway-specific manner in type 1 diabetes.TRIAL REGISTRATION: ClinicalTrials.gov NCT05095259.
AB - AIMS/HYPOTHESIS: As a result of early loss of the glucagon response, adrenaline is the primary counter-regulatory hormone in type 1 diabetes. Diminished adrenaline responses to hypoglycaemia due to counter-regulatory failure are common in type 1 diabetes, and are probably induced by exposure to recurrent hypoglycaemia, however, the metabolic effects of adrenaline have received less research attention, and also there is conflicting evidence regarding adrenaline sensitivity in type 1 diabetes. Thus, we aimed to investigate the metabolic response to adrenaline and explore whether it is modified by prior exposure to hypoglycaemia.METHODS: Eighteen participants with type 1 diabetes and nine healthy participants underwent a three-step ascending adrenaline infusion during a hyperinsulinaemic-euglycaemic clamp. Continuous glucose monitoring data obtained during the week before the study day were used to assess the extent of hypoglycaemia exposure.RESULTS: While glucose responses during the clamp were similar between people with type 1 diabetes and healthy participants, plasma concentrations of NEFAs and glycerol only increased in the group with type 1 diabetes (p<0.001). Metabolomics revealed an increase in the most common NEFAs (p<0.01). Other metabolic responses were generally similar between participants with type 1 diabetes and healthy participants. Exposure to hypoglycaemia was negatively associated with the NEFA response; however, this was not statistically significant.CONCLUSIONS/INTERPRETATION: In conclusion, individuals with type 1 diabetes respond with increased lipolysis to adrenaline compared with healthy participants by mobilising the abundant NEFAs in plasma, whereas other metabolic responses were similar. This may suggest that the metabolic sensitivity to adrenaline is altered in a pathway-specific manner in type 1 diabetes.TRIAL REGISTRATION: ClinicalTrials.gov NCT05095259.
KW - Clinical diabetes
KW - Hypoglycaemia
KW - Metabolic physiology in vivo
KW - Metabolomics
KW - Other hormones/action
KW - Pathophysiology/metabolism
KW - Glucagon/blood
KW - Blood Glucose/metabolism
KW - Humans
KW - Insulin/administration & dosage
KW - Fatty Acids, Nonesterified/blood
KW - Male
KW - Case-Control Studies
KW - Diabetes Mellitus, Type 1/drug therapy
KW - Glycerol/blood
KW - Young Adult
KW - Adult
KW - Epinephrine/blood
KW - Female
KW - Glucose Clamp Technique
KW - Hypoglycemia/blood
UR - http://www.scopus.com/inward/record.url?scp=85186487383&partnerID=8YFLogxK
U2 - 10.1007/s00125-024-06116-5
DO - 10.1007/s00125-024-06116-5
M3 - Journal article
C2 - 38427076
SN - 0012-186X
VL - 67
SP - 1095
EP - 1106
JO - Diabetologia
JF - Diabetologia
IS - 6
ER -