Abstract | AIM: MATERIALS AND METHODS: In a randomized, double-blinded, parallel-group trial, 108 individuals with type 1 diabetes aged 18 years or older on basal-bolus therapy with HbA1c 59-88 mmol/mol (7.5%-10.0%) and body mass index of more than 22.0 kg/m2 were randomized (1:1) to preprandial subcutaneous injection of 10 μg exenatide ( Byetta) before breakfast, lunch, and dinner over 26 weeks as add-on treatment to insulin therapy. RESULTS:
Exenatide elicited a body weight reduction of 4.4 kg compared with placebo, but no between-group differences in bone mineral density, as assessed by whole-body, hip, lumbar, and forearm dual-energy X-ray absorptiometry following 26 weeks of treatment, were observed. Fasting plasma levels of C-terminal telopeptides of type I collagen, a marker of bone resorption, and amino-terminal propeptide of type I procollagen, a marker of bone formation, were unchanged by exenatide compared with placebo after 26 weeks. CONCLUSIONS:
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Authors | Nicklas J Johansen, Thomas F Dejgaard, Asger Lund, Camilla Schlüntz, Bolette Hartmann, Jens J Holst, Tina Vilsbøll, Henrik U Andersen, Filip K Knop |
Journal | Diabetes, obesity & metabolism
(Diabetes Obes Metab)
Vol. 24
Issue 2
Pg. 221-227
(02 2022)
ISSN: 1463-1326 [Electronic] England |
PMID | 34617375
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | © 2021 John Wiley & Sons Ltd. |
Chemical References |
- Blood Glucose
- Glycated Hemoglobin A
- Hypoglycemic Agents
- Insulin
- Venoms
- Exenatide
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Topics |
- Adolescent
- Blood Glucose
(metabolism)
- Diabetes Mellitus, Type 1
(drug therapy)
- Diabetes Mellitus, Type 2
(drug therapy)
- Exenatide
(therapeutic use)
- Glycated Hemoglobin
(analysis)
- Humans
- Hypoglycemic Agents
(pharmacology, therapeutic use)
- Insulin
(therapeutic use)
- Venoms
(therapeutic use)
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