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Dasiglucagon Effectively Mitigates Postbariatric Postprandial Hypoglycemia: A Randomized, Double-Blind, Placebo-Controlled, Crossover Trial.

AbstractOBJECTIVE:
To investigate the efficacy and safety of dasiglucagon, a novel stable glucagon analog in a liquid formulation, in Roux-en-Y gastric bypass (RYGB)-operated individuals suffering from postbariatric hypoglycemia (PBH).
RESEARCH DESIGN AND METHODS:
In a randomized, double-blind, placebo-controlled, crossover trial, 10 RYGB-operated participants with continuous glucose monitoring-verified PBH were randomly assigned to 3 trial days, each consisting of a 240-min standardized liquid mixed-meal test with the subcutaneous injection of placebo or 80 μg or 200 μg dasiglucagon.
RESULTS:
Compared with placebo, treatment with both 80 and 200 μg dasiglucagon raised nadir plasma glucose (PG) (placebo: 3.0 ± 0.2 mmol/L [mean ± SEM]; 80 μg dasiglucagon: 3.9 ± 0.3 mmol/L, P = 0.002; 200 μg dasiglucagon: 4.5 ± 0.2 mmol/L, P = 0.0002) and reduced time in hypoglycemia (PG <3.9 mmol/L) by 70.0 min (P = 0.030 and P = 0.008).
CONCLUSIONS:
Single-dose administration of dasiglucagon effectively mitigated postprandial hypoglycemia.
AuthorsCasper K Nielsen, Caroline C Øhrstrøm, Urd L Kielgast, Dorte L Hansen, Bolette Hartmann, Jens J Holst, Asger Lund, Tina Vilsbøll, Filip K Knop
JournalDiabetes care (Diabetes Care) Vol. 45 Issue 6 Pg. 1476-1481 (06 02 2022) ISSN: 1935-5548 [Electronic] United States
PMID35320361 (Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Copyright© 2022 by the American Diabetes Association.
Chemical References
  • Blood Glucose
  • Insulin
  • dasiglucagon
  • Glucagon
Topics
  • Blood Glucose
  • Blood Glucose Self-Monitoring
  • Cross-Over Studies
  • Double-Blind Method
  • Gastric Bypass (adverse effects)
  • Glucagon (analogs & derivatives)
  • Humans
  • Hypoglycemia (drug therapy, etiology, prevention & control)
  • Insulin (therapeutic use)

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