التفاصيل البيبلوغرافية
العنوان: |
Dual glucagon‐like peptide‐1 receptor/glucagon receptor agonist SAR425899 improves beta‐cell function in type 2 diabetes |
المؤلفون: |
Visentin, Roberto, Schiavon, Michele, Göbel, Britta, Riz, Michela, Cobelli, Claudio, Klabunde, Thomas, Dalla Man, Chiara |
المساهمون: |
Sanofi |
المصدر: |
Diabetes, Obesity and Metabolism ; volume 22, issue 4, page 640-647 ; ISSN 1462-8902 1463-1326 |
بيانات النشر: |
Wiley |
سنة النشر: |
2019 |
المجموعة: |
Wiley Online Library (Open Access Articles via Crossref) |
الوصف: |
Aim To evaluate the change in insulin sensitivity, β‐cell function and glucose absorption after 28 days of treatment with high and low doses of SAR425899, a novel dual glucagon‐like peptide‐1 receptor/glucagon receptor agonist, versus placebo. Materials and Methods Thirty‐six overweight to obese subjects with type 2 diabetes were randomized to receive daily subcutaneous administrations of low‐dose SAR425899 (0.03, 0.06 and 0.09 mg) and high‐dose SAR425899 (0.06, 0.12 and 0.18 mg) or placebo for 28 days; dose escalation occurred after days 7 and 14. Mixed meal tolerance tests were conducted before treatment (day −1) and on days 1 and 28. Oral glucose and C‐peptide minimal models were used to quantify metabolic indices of insulin sensitivity, β‐cell responsiveness and glucose absorption. Results With low‐dose SAR425899, high‐dose SAR425899 and placebo, β‐cell function from day −1 to day 28 increased by 163%, 95% and 23%, respectively. The change in area under the curve for the rate of meal glucose appearance between 0 and 120 minutes was −32%, −20% and 8%, respectively. Conclusions After 28 days of treatment, SAR425899 improved postprandial glucose control by significantly enhancing β‐cell function and slowing glucose absorption rate. |
نوع الوثيقة: |
article in journal/newspaper |
اللغة: |
English |
DOI: |
10.1111/dom.13939 |
الإتاحة: |
https://doi.org/10.1111/dom.13939Test |
حقوق: |
http://onlinelibrary.wiley.com/termsAndConditions#vorTest |
رقم الانضمام: |
edsbas.9D1E80EC |
قاعدة البيانات: |
BASE |