The dipeptidyl peptidase-4 inhibitor linagliptin lowers postprandial glucose and improves measures ofβ-cell function in type 2 diabetes
Autor: | Hans-Juergen Woerle, Uwe Hehnke, M. Larbig, Klaus Dugi, Tim Heise, Thomas Seck, Sanjay Patel |
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Rok vydání: | 2014 |
Předmět: |
medicine.medical_specialty
endocrine system diseases Surrogate endpoint business.industry Endocrinology Diabetes and Metabolism nutritional and metabolic diseases Type 2 Diabetes Mellitus Dipeptidyl peptidase-4 inhibitor Type 2 diabetes Linagliptin medicine.disease Placebo Endocrinology Postprandial Internal medicine Internal Medicine medicine Beta cell business medicine.drug |
Zdroj: | Diabetes, Obesity and Metabolism. 16:1036-1039 |
ISSN: | 1462-8902 |
Popis: | Progressive deterioration of pancreatic β-cell function in patients with type 2 diabetes mellitus (T2DM) contributes to worsening of hyperglycaemia. To investigate the effects of the dipeptidyl peptidase-4 inhibitor linagliptin on β-cell function parameters, a pooled analysis of six randomized, 24-week, placebo-controlled, phase 3 trials of 5 mg of linagliptin daily was performed in 2701 patients with T2DM (linagliptin, n = 1905; placebo, n = 796). At week 24, observed improvements in HbA1c, fasting plasma glucose, and 2-h postprandial glucose were significantly greater for linagliptin than placebo (all p < 0.0001). Homeostasis model assessment (HOMA)-%β, as a surrogate marker of fasting β-cell function, was significantly improved with linagliptin, and did not change with placebo (placebo-adjusted mean ± s.e. change for linagliptin: 16.5 ± 4.6 (mU/l)/(mmol/l); p = 0.0003). Further study is required to determine if the significant improvement in HOMA-%β with linagliptin will translate into long-term improvements in β-cell function. |
Databáze: | OpenAIRE |
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