Abstract | OBJECTIVE: 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:
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Authors | Casper K Nielsen, Caroline C Øhrstrøm, Urd L Kielgast, Dorte L Hansen, Bolette Hartmann, Jens J Holst, Asger Lund, Tina Vilsbøll, Filip K Knop |
Journal | Diabetes care
(Diabetes Care)
Vol. 45
Issue 6
Pg. 1476-1481
(06 02 2022)
ISSN: 1935-5548 [Electronic] United States |
PMID | 35320361
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | © 2022 by the American Diabetes Association. |
Chemical References |
- Blood Glucose
- Insulin
- dasiglucagon
- Glucagon
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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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