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Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy

(J Diabetes Invest, doi: 10.1111/j.2040‐1124.2012.00223.x, 2012) Aims/Introduction:  We assessed the efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy (BOT). Materials and Methods:  We retrospectively analyzed the data of...

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Autores principales: Takahara, Mitsuyoshi, Shiraiwa, Toshihiko, Ohtoshi, Kentaro, Kaneto, Hideaki, Katakami, Naoto, Matsuoka, Taka‐aki, Shimomura, Iichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015430/
https://www.ncbi.nlm.nih.gov/pubmed/24843616
http://dx.doi.org/10.1111/j.2040-1124.2012.00223.x
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author Takahara, Mitsuyoshi
Shiraiwa, Toshihiko
Ohtoshi, Kentaro
Kaneto, Hideaki
Katakami, Naoto
Matsuoka, Taka‐aki
Shimomura, Iichiro
author_facet Takahara, Mitsuyoshi
Shiraiwa, Toshihiko
Ohtoshi, Kentaro
Kaneto, Hideaki
Katakami, Naoto
Matsuoka, Taka‐aki
Shimomura, Iichiro
author_sort Takahara, Mitsuyoshi
collection PubMed
description (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2012.00223.x, 2012) Aims/Introduction:  We assessed the efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy (BOT). Materials and Methods:  We retrospectively analyzed the data of 37 patients who had postprandial hyperglycemia (≥10.0 mmol/L) with BOT (long‐acting insulin plus glimepiride) with their insulin titrated enough to keep preprandial glycemia <7.2 mmol/L, and who had their treatment changed to liraglutide monotherapy, with the subsequent addition of glimepiride, when required. Those who achieved the glycemic target at all points (preprandial glycemia <7.2 mmol/L and postprandial glycemia <10.0 mmol/L) were regarded as responders and the efficacy of liraglutide therapy was assessed. We also explored the predictive clinical characteristics associated with its efficacy. Results:  Daily doses of insulin and glimepiride with BOT were 14 ± 9 units and 1.5 ± 0.9 mg, respectively. After the change to liraglutide therapy, 37% of the patients appeared to be responders to the therapy, whereas 12% had their glycemic control rather deteriorated. Efficacy of liraglutide therapy was significantly associated with baseline insulin dosage and post‐breakfast glycemia with BOT. The C‐statistic of the model was calculated to be 0.90. Conclusions:  There were responders and non‐responders to liraglutide therapy in Japanese BOT failures. It is likely that baseline insulin dosage and post‐breakfast glycemia with BOT are clinically useful indicators for the efficacy of liraglutide therapy.
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spelling pubmed-40154302014-05-19 Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy Takahara, Mitsuyoshi Shiraiwa, Toshihiko Ohtoshi, Kentaro Kaneto, Hideaki Katakami, Naoto Matsuoka, Taka‐aki Shimomura, Iichiro J Diabetes Investig Articles (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2012.00223.x, 2012) Aims/Introduction:  We assessed the efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy (BOT). Materials and Methods:  We retrospectively analyzed the data of 37 patients who had postprandial hyperglycemia (≥10.0 mmol/L) with BOT (long‐acting insulin plus glimepiride) with their insulin titrated enough to keep preprandial glycemia <7.2 mmol/L, and who had their treatment changed to liraglutide monotherapy, with the subsequent addition of glimepiride, when required. Those who achieved the glycemic target at all points (preprandial glycemia <7.2 mmol/L and postprandial glycemia <10.0 mmol/L) were regarded as responders and the efficacy of liraglutide therapy was assessed. We also explored the predictive clinical characteristics associated with its efficacy. Results:  Daily doses of insulin and glimepiride with BOT were 14 ± 9 units and 1.5 ± 0.9 mg, respectively. After the change to liraglutide therapy, 37% of the patients appeared to be responders to the therapy, whereas 12% had their glycemic control rather deteriorated. Efficacy of liraglutide therapy was significantly associated with baseline insulin dosage and post‐breakfast glycemia with BOT. The C‐statistic of the model was calculated to be 0.90. Conclusions:  There were responders and non‐responders to liraglutide therapy in Japanese BOT failures. It is likely that baseline insulin dosage and post‐breakfast glycemia with BOT are clinically useful indicators for the efficacy of liraglutide therapy. Blackwell Publishing Ltd 2012-06-26 2012-12-20 /pmc/articles/PMC4015430/ /pubmed/24843616 http://dx.doi.org/10.1111/j.2040-1124.2012.00223.x Text en © 2012 Asian Association for the Study of Diabetes and Wiley Publishing Asia Pty Ltd
spellingShingle Articles
Takahara, Mitsuyoshi
Shiraiwa, Toshihiko
Ohtoshi, Kentaro
Kaneto, Hideaki
Katakami, Naoto
Matsuoka, Taka‐aki
Shimomura, Iichiro
Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy
title Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy
title_full Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy
title_fullStr Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy
title_full_unstemmed Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy
title_short Efficacy of liraglutide therapy in Japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy
title_sort efficacy of liraglutide therapy in japanese type 2 diabetic patients insufficiently controlled with basal‐supported oral therapy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015430/
https://www.ncbi.nlm.nih.gov/pubmed/24843616
http://dx.doi.org/10.1111/j.2040-1124.2012.00223.x
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