期刊论文详细信息
Journal of Diabetes Investigation
The once‐daily human glucagon‐like peptide‐1 analog, liraglutide, improves β‐cell function in Japanese patients with type 2 diabetes
Yutaka Seino2  Mads Frederik Rasmussen1  Per Clauson3 
[1] Global Development, Novo Nordisk A/S, Søborg, Denmark;Kansai Electric Power Hospital, Osaka;Development Division, Novo Nordisk Pharma Ltd, Tokyo
关键词: Insulin‐secreting cells;    Liraglutide;    Type 2 diabetes;   
DOI  :  10.1111/j.2040-1124.2012.00193.x
来源: Wiley
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【 摘 要 】

Abstract

Aims/Introduction:  β-cell function was evaluated by homeostasis model assessment of β-cell function (HOMA-B) index, proinsulin:insulin and proinsulin:C-peptide ratios in adult, Japanese type 2 diabetes patients receiving liraglutide.

Materials and Methods:  Data from two randomized, controlled clinical trials (A and B) including 664 Japanese type 2 diabetes patients (mean values: glycated hemoglobin [HbA1c] 8.61–9.32%; body mass index [BMI] 24.4–25.3 kg/m2) were analyzed. In two 24-week trials, patients received liraglutide 0.9 mg (= 268) or glibenclamide 2.5 mg (= 132; trial A), or liraglutide 0.6, 0.9 mg (= 176) or placebo (= 88) added to previous sulfonylurea therapy (trial B).

Results:  Liraglutide was associated with improved glycemic control vs sulfonylurea monotherapy or placebo. In liraglutide-treated groups in trials A and B, area under the curve (AUC) insulin 0–3 h was improved (< 0.001 for all) and the AUCinsulin 0–3 h:AUCglucose 0–3 h ratio was increased (estimated treatment difference [liraglutide–comparator] 0.058 [0.036, 0.079]). HOMA-B significantly increased with liraglutide relative to comparator in trial B (< 0.05), but not in trial A. The reduction in fasting proinsulin:insulin ratio was 50% greater than in comparator groups.

Conclusions:  In Japanese type 2 diabetes patients, liraglutide was associated with effective glycemic control, restoration of prandial insulin response and indications of improved β-cell function. This trial was registered with Clinicaltrials.gov (trial A: no. NCT00393718/JapicCTI-060328 and trial B: no. NCT00395746/JapicCTI-060324). (J Diabetes Invest, doi: 10.1111/j.2040-1124.2012.00193.x, 2012)

【 授权许可】

Unknown   
© 2012 Asian Association for the Study of Diabetes and Blackwell Publishing Asia Pty Ltd

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