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Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients

Saxagliptin is a selective and potent dipeptidyl peptidase (DPP)-4 inhibitor, approved as an adjunct to diet and exercise to improve glycemic control in type 2 diabetes mellitus (T2DM) in the USA on July 2009, and had been launched globally in over 86 countries by September 2013. In patients with T2...

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Autores principales: Konya, Hiroyuki, Yano, Yuzo, Matsutani, Satoshi, Tsunoda, Taku, Ikawa, Takashi, Kusunoki, Yoshiki, Matsuo, Toshihiro, Miuchi, Masayuki, Katsuno, Tomoyuki, Hamaguchi, Tomoya, Miyagawa, Jun-ichiro, Namba, Mitsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103926/
https://www.ncbi.nlm.nih.gov/pubmed/25050065
http://dx.doi.org/10.2147/TCRM.S46076
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author Konya, Hiroyuki
Yano, Yuzo
Matsutani, Satoshi
Tsunoda, Taku
Ikawa, Takashi
Kusunoki, Yoshiki
Matsuo, Toshihiro
Miuchi, Masayuki
Katsuno, Tomoyuki
Hamaguchi, Tomoya
Miyagawa, Jun-ichiro
Namba, Mitsuyoshi
author_facet Konya, Hiroyuki
Yano, Yuzo
Matsutani, Satoshi
Tsunoda, Taku
Ikawa, Takashi
Kusunoki, Yoshiki
Matsuo, Toshihiro
Miuchi, Masayuki
Katsuno, Tomoyuki
Hamaguchi, Tomoya
Miyagawa, Jun-ichiro
Namba, Mitsuyoshi
author_sort Konya, Hiroyuki
collection PubMed
description Saxagliptin is a selective and potent dipeptidyl peptidase (DPP)-4 inhibitor, approved as an adjunct to diet and exercise to improve glycemic control in type 2 diabetes mellitus (T2DM) in the USA on July 2009, and had been launched globally in over 86 countries by September 2013. In patients with T2DM, once-daily administration of saxagliptin before breakfast achieves sustained inhibition of plasma DPP-4 activity and reduction of postprandial hyperglycemia, including after dinner, associated with an increase in plasma glucagon-like peptide-1 levels. This paper reviews the safety and efficacy of saxagliptin in Japanese patients with T2DM. The clinical development study in Japan supported its usefulness for the disease. Saxagliptin 1, 2.5, and 5 mg led to significant improvements in glycated hemoglobin (HbA(1c)), and was generally well tolerated. Treatment with saxagliptin 5 mg induced a sustained reduction in HbA(1c) over 52 weeks. Long-term combination therapy with saxagliptin and other oral hypoglycemic agents also provided sustained glycemic control and was well tolerated for up to 52 weeks. Saxagliptin as add-on to sulfonylureas or glinides has a tendency to increase hypoglycemia, but not with other oral antidiabetic agents, such as α-glucosidase inhibitors, metformin, or thiazolidinediones. The results of clinical trials have confirmed the long-term efficacy and safety of saxagliptin monotherapy as well as its use as add-on combination therapy, and support its usefulness as a therapeutic agent for T2DM. Saxagliptin has less concern for hypoglycemia and weight gain, which often becomes problematic in routine care of T2DM. Meta-analysis of clinical trials in the USA showed no evidence of increased risk of cardiovascular events associated with saxagliptin, suggesting the superior of saxagliptin in terms of safety. Recently, investigators in the SAVOR-TIMI (Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with Diabetes Mellitus-Thrombolysis in Myocardial Infarction) 53 study suggested that DPP-4 inhibition with saxagliptin did not increase or decrease the rate of ischemic events, although the rate of hospitalization for heart failure was increased. Although saxagliptin improves glycemic control, other approaches are necessary to reduce cardiovascular risk in patients with diabetes. Saxagliptin is applicable for various pathological conditions, and is considered to be clinically significant as a new therapeutic option for Japanese patients with T2DM.
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spelling pubmed-41039262014-07-21 Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients Konya, Hiroyuki Yano, Yuzo Matsutani, Satoshi Tsunoda, Taku Ikawa, Takashi Kusunoki, Yoshiki Matsuo, Toshihiro Miuchi, Masayuki Katsuno, Tomoyuki Hamaguchi, Tomoya Miyagawa, Jun-ichiro Namba, Mitsuyoshi Ther Clin Risk Manag Review Saxagliptin is a selective and potent dipeptidyl peptidase (DPP)-4 inhibitor, approved as an adjunct to diet and exercise to improve glycemic control in type 2 diabetes mellitus (T2DM) in the USA on July 2009, and had been launched globally in over 86 countries by September 2013. In patients with T2DM, once-daily administration of saxagliptin before breakfast achieves sustained inhibition of plasma DPP-4 activity and reduction of postprandial hyperglycemia, including after dinner, associated with an increase in plasma glucagon-like peptide-1 levels. This paper reviews the safety and efficacy of saxagliptin in Japanese patients with T2DM. The clinical development study in Japan supported its usefulness for the disease. Saxagliptin 1, 2.5, and 5 mg led to significant improvements in glycated hemoglobin (HbA(1c)), and was generally well tolerated. Treatment with saxagliptin 5 mg induced a sustained reduction in HbA(1c) over 52 weeks. Long-term combination therapy with saxagliptin and other oral hypoglycemic agents also provided sustained glycemic control and was well tolerated for up to 52 weeks. Saxagliptin as add-on to sulfonylureas or glinides has a tendency to increase hypoglycemia, but not with other oral antidiabetic agents, such as α-glucosidase inhibitors, metformin, or thiazolidinediones. The results of clinical trials have confirmed the long-term efficacy and safety of saxagliptin monotherapy as well as its use as add-on combination therapy, and support its usefulness as a therapeutic agent for T2DM. Saxagliptin has less concern for hypoglycemia and weight gain, which often becomes problematic in routine care of T2DM. Meta-analysis of clinical trials in the USA showed no evidence of increased risk of cardiovascular events associated with saxagliptin, suggesting the superior of saxagliptin in terms of safety. Recently, investigators in the SAVOR-TIMI (Saxagliptin Assessment of Vascular Outcomes Recorded in Patients with Diabetes Mellitus-Thrombolysis in Myocardial Infarction) 53 study suggested that DPP-4 inhibition with saxagliptin did not increase or decrease the rate of ischemic events, although the rate of hospitalization for heart failure was increased. Although saxagliptin improves glycemic control, other approaches are necessary to reduce cardiovascular risk in patients with diabetes. Saxagliptin is applicable for various pathological conditions, and is considered to be clinically significant as a new therapeutic option for Japanese patients with T2DM. Dove Medical Press 2014-07-11 /pmc/articles/PMC4103926/ /pubmed/25050065 http://dx.doi.org/10.2147/TCRM.S46076 Text en © 2014 Konya et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Konya, Hiroyuki
Yano, Yuzo
Matsutani, Satoshi
Tsunoda, Taku
Ikawa, Takashi
Kusunoki, Yoshiki
Matsuo, Toshihiro
Miuchi, Masayuki
Katsuno, Tomoyuki
Hamaguchi, Tomoya
Miyagawa, Jun-ichiro
Namba, Mitsuyoshi
Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients
title Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients
title_full Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients
title_fullStr Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients
title_full_unstemmed Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients
title_short Profile of saxagliptin in the treatment of type 2 diabetes: focus on Japanese patients
title_sort profile of saxagliptin in the treatment of type 2 diabetes: focus on japanese patients
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103926/
https://www.ncbi.nlm.nih.gov/pubmed/25050065
http://dx.doi.org/10.2147/TCRM.S46076
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