We have reported that the HbA1c‐lowering effects of liraglutide/basal insulin combination rely on remaining β‐cell function and that the cut‐off value of the C‐peptide immunoreactivity index (CPI), a β‐cell function‐related index frequently used in Japanese clinical settings, is 1.103 for the achievement of HbA1c <7.0% at 54 weeks after initiating the liraglutide/basal insulin combination. Wilbrink et al claimed that glucose‐lowering effects of glucagon‐like peptide‐1 receptor agonist liraglutide depend of duration of type 2 diabetes; while our resent study published in the Journal of Diabetes Investigation failed to detect such dependency. This discrepancy might be due to several reasons including co‐administration of basal insulin with li...
AIM: To evaluate, using post hoc analyses, whether the novel combination of a basal insulin, insulin...
The study by Balkau et al. (1) finds that people who are thinner and have more poorly controlled dia...
We have read the study by Kramer et al. (1) concerning glucagon response to oral glucose challenge i...
Aims/Introduction: The glucose‐lowering effects of the glucagon‐like peptide‐1 receptor agonist, lir...
Aims: To evaluate the glycaemic control of combination therapy with basal insulin and liraglutide, a...
AbstractAimsThe GLP-1 receptor agonist liraglutide improves impaired pancreatic β-cell function, the...
We read with interest the results of the A1chieve study (1), a noninterventional, observational, 24-...
Contains fulltext : 198072.pdf (publisher's version ) (Open Access)Comment on the ...
AbstractWe searched for factors influencing the clinical effects of GLP-1 analogue liraglutide in su...
Item does not contain fulltextAIMS/HYPOTHESIS: The best treatment strategy for a patient with type 2...
Chaudhuri et al. (1) raised the question of why exenatide increased insulin sensi-tivity in our pati...
Item does not contain fulltextBACKGROUND: Pronounced weight gain frequently complicates insulin ther...
IntroductionTreatments for type 2 diabetes targeting baseline glucose levels but not postprandial gl...
To the Editor The paper by Jones et al. in which they studied the response of a cohort of 19 patie...
Aims: To evaluate the glycaemic control of combination therapy with basal insulin and liraglutide, a...
AIM: To evaluate, using post hoc analyses, whether the novel combination of a basal insulin, insulin...
The study by Balkau et al. (1) finds that people who are thinner and have more poorly controlled dia...
We have read the study by Kramer et al. (1) concerning glucagon response to oral glucose challenge i...
Aims/Introduction: The glucose‐lowering effects of the glucagon‐like peptide‐1 receptor agonist, lir...
Aims: To evaluate the glycaemic control of combination therapy with basal insulin and liraglutide, a...
AbstractAimsThe GLP-1 receptor agonist liraglutide improves impaired pancreatic β-cell function, the...
We read with interest the results of the A1chieve study (1), a noninterventional, observational, 24-...
Contains fulltext : 198072.pdf (publisher's version ) (Open Access)Comment on the ...
AbstractWe searched for factors influencing the clinical effects of GLP-1 analogue liraglutide in su...
Item does not contain fulltextAIMS/HYPOTHESIS: The best treatment strategy for a patient with type 2...
Chaudhuri et al. (1) raised the question of why exenatide increased insulin sensi-tivity in our pati...
Item does not contain fulltextBACKGROUND: Pronounced weight gain frequently complicates insulin ther...
IntroductionTreatments for type 2 diabetes targeting baseline glucose levels but not postprandial gl...
To the Editor The paper by Jones et al. in which they studied the response of a cohort of 19 patie...
Aims: To evaluate the glycaemic control of combination therapy with basal insulin and liraglutide, a...
AIM: To evaluate, using post hoc analyses, whether the novel combination of a basal insulin, insulin...
The study by Balkau et al. (1) finds that people who are thinner and have more poorly controlled dia...
We have read the study by Kramer et al. (1) concerning glucagon response to oral glucose challenge i...