Skip to main content
Top
Published in: Clinical and Experimental Nephrology 1/2013

01-02-2013 | Review Article

New strategy for the treatment of type 2 diabetes mellitus with incretin-based therapy

Authors: Mitsuyoshi Namba, Tomoyuki Katsuno, Yoshiki Kusunoki, Toshihiro Matsuo, Masayuki Miuchi, Jun-ichiro Miyagawa

Published in: Clinical and Experimental Nephrology | Issue 1/2013

Login to get access

Abstract

Incretin-based therapy was first made available for the treatment of type 2 diabetes mellitus (T2DM) in the US in 2006 and in Japan in 2009. Four DPP-4 inhibitors and two GLP-1 analog/receptor agonists are currently available. The effects of incretin-based therapy are assumed to be exerted mainly through the hormonal and neuronal actions of one of the incretins, GLP-1, which is secreted from L cells localized in the small intestine. The benefits of this therapy over conventional sulfonylureas or insulin injections, such as fewer hypoglycemic events and reduced body weight gain, derive from the glucose-dependent insulinotropic effect. The protective effects of this therapy on vulnerable pancreatic β-cells and against micro/macroangiopathy in T2DM are also most welcome. Indications and/or contraindications for incretin-based therapy should be clarified by prospectively studying the experiences of Japanese T2DM patients undergoing this therapy in the clinical setting.
Literature
2.
go back to reference Tripathy D, Carlsson M, Almgren P, Isomaa B, Taskinen M-R, Tuomi T, Groop LC. Insulin secretion and insulin sensitivity in relation to glucose tolerance—lessons from the Botnia study. Diabetes. 2000;49:975–80.PubMedCrossRef Tripathy D, Carlsson M, Almgren P, Isomaa B, Taskinen M-R, Tuomi T, Groop LC. Insulin secretion and insulin sensitivity in relation to glucose tolerance—lessons from the Botnia study. Diabetes. 2000;49:975–80.PubMedCrossRef
3.
go back to reference Fukushima M, Suzuki H, Seino Y. Insulin secretion capacity in the development from normal glucose tolerance to type 2 diabetes. Diabetes Res Clin Pract. 2004;66S:S37–43.CrossRef Fukushima M, Suzuki H, Seino Y. Insulin secretion capacity in the development from normal glucose tolerance to type 2 diabetes. Diabetes Res Clin Pract. 2004;66S:S37–43.CrossRef
4.
go back to reference Unger RH, Cherrington AD. Glucagonocentric restructuring of diabetes: a pathophysiologic and therapeutic makeover. J Clin Invest. 2012;122:4–12.PubMedCrossRef Unger RH, Cherrington AD. Glucagonocentric restructuring of diabetes: a pathophysiologic and therapeutic makeover. J Clin Invest. 2012;122:4–12.PubMedCrossRef
5.
go back to reference Miuchi M, Miyagawa J-I, Konishi K, Nagai E, Matsuo T, Murai K, Katsuno T, Hamaguchi T Namba M. Morphologic changes of α-cells in the pancreas of Japanese non-obese type 2 diabetes (oral presentation). In: 3rd Scientific Meeting of the Asian Association for the Study of Diabetes. Tokyo: AASD; 2011. Miuchi M, Miyagawa J-I, Konishi K, Nagai E, Matsuo T, Murai K, Katsuno T, Hamaguchi T Namba M. Morphologic changes of α-cells in the pancreas of Japanese non-obese type 2 diabetes (oral presentation). In: 3rd Scientific Meeting of the Asian Association for the Study of Diabetes. Tokyo: AASD; 2011.
6.
go back to reference Gautier JF, Fetita S, Sobngwi E, Salaun-Martin C. Biological actions of the incretins GIP and GLP-1 and therapeutic perspectives in patients with type 2 diabetes. Diabetes Metab. 2005;31:233–42.PubMedCrossRef Gautier JF, Fetita S, Sobngwi E, Salaun-Martin C. Biological actions of the incretins GIP and GLP-1 and therapeutic perspectives in patients with type 2 diabetes. Diabetes Metab. 2005;31:233–42.PubMedCrossRef
7.
go back to reference Zhao T, Parikh P, Bhashyam S, Bolukoglu H, Poornimal I, Shen YT, Shannon RP. Direct effcts of glucagon-like peptide-1 on myocardial contractlity and glucose uptake in normal and postischemic isolated rat hearts. J Pharmacol Exp Ther. 2006;317:1106–13.PubMedCrossRef Zhao T, Parikh P, Bhashyam S, Bolukoglu H, Poornimal I, Shen YT, Shannon RP. Direct effcts of glucagon-like peptide-1 on myocardial contractlity and glucose uptake in normal and postischemic isolated rat hearts. J Pharmacol Exp Ther. 2006;317:1106–13.PubMedCrossRef
8.
go back to reference Nystrom T, Gutniak MK, Zhang Q, Zhang F, Holst JJ, Ahren B, Sjoholm A. Effects of glucagon-like peptide-1 on endotherail function in type 2 diabetes patients with stable coronary artery disease. Am J Physiol Endocrinol Metab. 2004;287:E1209–15.PubMedCrossRef Nystrom T, Gutniak MK, Zhang Q, Zhang F, Holst JJ, Ahren B, Sjoholm A. Effects of glucagon-like peptide-1 on endotherail function in type 2 diabetes patients with stable coronary artery disease. Am J Physiol Endocrinol Metab. 2004;287:E1209–15.PubMedCrossRef
9.
go back to reference van Poppel PC, Netea MG, Smith P, Tack CJ. Vildagliptin improves endothelium-dependent vasodilation in type 2 diabetes. Diabetes Care. 2011;34:2072–7.PubMedCrossRef van Poppel PC, Netea MG, Smith P, Tack CJ. Vildagliptin improves endothelium-dependent vasodilation in type 2 diabetes. Diabetes Care. 2011;34:2072–7.PubMedCrossRef
10.
go back to reference Perry T, Haughey NJ, Mattson MP, Egan JM, Greig NH. Protection and reversal of excitotoxic neuronal damage by glucagon-like peptide-1 and exendin-4. J Pharmacol Exp Ther. 2002;302:881–8.PubMedCrossRef Perry T, Haughey NJ, Mattson MP, Egan JM, Greig NH. Protection and reversal of excitotoxic neuronal damage by glucagon-like peptide-1 and exendin-4. J Pharmacol Exp Ther. 2002;302:881–8.PubMedCrossRef
11.
go back to reference Kodera R, Shikata K, Kataoka HU, Takatsuka T, Miyamoto S, Sasaki M, Kajitani N, Nishishita S, Sarai K, Hirota D, Sato C, Ogawa D, Makinjo H. Glucagon-like peptide-1 receptor agonist ameliorates renal injury through its anti-inflammatory action without lowering blood glucose level in a rat model of type 1 diabetes. Diabetologia. 2011;54:965–78. Kodera R, Shikata K, Kataoka HU, Takatsuka T, Miyamoto S, Sasaki M, Kajitani N, Nishishita S, Sarai K, Hirota D, Sato C, Ogawa D, Makinjo H. Glucagon-like peptide-1 receptor agonist ameliorates renal injury through its anti-inflammatory action without lowering blood glucose level in a rat model of type 1 diabetes. Diabetologia. 2011;54:965–78.
12.
go back to reference Ishibashi Y, Nishino Y, Matsui T, Takeuchi M, Yamagishi S. Glucago-like peptide-1 suppresses advanced glycation end product-induced monocyte chemoattractant protein-1 expression in mesangial cells by reducing advanced glycation end product receptor level. Metabolism. 2011;60:1271–7.PubMedCrossRef Ishibashi Y, Nishino Y, Matsui T, Takeuchi M, Yamagishi S. Glucago-like peptide-1 suppresses advanced glycation end product-induced monocyte chemoattractant protein-1 expression in mesangial cells by reducing advanced glycation end product receptor level. Metabolism. 2011;60:1271–7.PubMedCrossRef
13.
go back to reference Katsuno T, Kusunoki Y, Tokuda M, Murai K, Ochi F, Miuchi M, Hamaguchi T, Miyagawa J-i Namba M. Strict glycemic control in Japanese type 2 diabetes patients with incretin-based therapy—efficacy of continuous glucose monitoring for the secure transition and fine tuning. Infusyst Asia. 2012;7(1):6–8. Katsuno T, Kusunoki Y, Tokuda M, Murai K, Ochi F, Miuchi M, Hamaguchi T, Miyagawa J-i Namba M. Strict glycemic control in Japanese type 2 diabetes patients with incretin-based therapy—efficacy of continuous glucose monitoring for the secure transition and fine tuning. Infusyst Asia. 2012;7(1):6–8.
14.
go back to reference Blech S, Ludwig-Scwellinger E, Grafe-Mody EU, Withopf B, Wagner K. The metabolism and disposition of the oral dipeptidyl peptidase-4 inhibitor, linagliptin, in humans. Drug Metab Dispos. 2010;38:667–8.PubMedCrossRef Blech S, Ludwig-Scwellinger E, Grafe-Mody EU, Withopf B, Wagner K. The metabolism and disposition of the oral dipeptidyl peptidase-4 inhibitor, linagliptin, in humans. Drug Metab Dispos. 2010;38:667–8.PubMedCrossRef
15.
go back to reference Vincent SH, Reed JR, Bergman AJ, Elmore CS, Zhu B, Xu S, Ebel D, Larson P, Zeng W, Chen L, Dilzer S, Lasseter K, Gottesdiener K, Wagner JA, Herman GA. Metabolism and excretion of the dipeptidyl peptidase 4 inhibitor sitagliptin in humans. Drug Metab Dispos. 2007;35:533–8.PubMedCrossRef Vincent SH, Reed JR, Bergman AJ, Elmore CS, Zhu B, Xu S, Ebel D, Larson P, Zeng W, Chen L, Dilzer S, Lasseter K, Gottesdiener K, Wagner JA, Herman GA. Metabolism and excretion of the dipeptidyl peptidase 4 inhibitor sitagliptin in humans. Drug Metab Dispos. 2007;35:533–8.PubMedCrossRef
16.
go back to reference He H, Tran P, Yin H, Smith H, Batard Y, Wang L, Einolf H, Gu H, Mangold JB, Fischer V, Howard D. Absorption, metabolism and excretion of vildagliptin, a novel dipeptidyl peptidase 4 inhibitor, in humans. Drug Metab Dispos. 2009;37:536–44.PubMedCrossRef He H, Tran P, Yin H, Smith H, Batard Y, Wang L, Einolf H, Gu H, Mangold JB, Fischer V, Howard D. Absorption, metabolism and excretion of vildagliptin, a novel dipeptidyl peptidase 4 inhibitor, in humans. Drug Metab Dispos. 2009;37:536–44.PubMedCrossRef
17.
go back to reference Christopher R, Covington P, Davenport M, Fleck P, Mekki QA, Wann ER, Karim A. Pharmacokinetics, pharmacodymamics, and tolerability of single increasing doses of the dipeptidyl peptidase-4 inhibitor alogliptin in healthy male subjects. Clin Ther. 2008;30:513–27.PubMedCrossRef Christopher R, Covington P, Davenport M, Fleck P, Mekki QA, Wann ER, Karim A. Pharmacokinetics, pharmacodymamics, and tolerability of single increasing doses of the dipeptidyl peptidase-4 inhibitor alogliptin in healthy male subjects. Clin Ther. 2008;30:513–27.PubMedCrossRef
Metadata
Title
New strategy for the treatment of type 2 diabetes mellitus with incretin-based therapy
Authors
Mitsuyoshi Namba
Tomoyuki Katsuno
Yoshiki Kusunoki
Toshihiro Matsuo
Masayuki Miuchi
Jun-ichiro Miyagawa
Publication date
01-02-2013
Publisher
Springer Japan
Published in
Clinical and Experimental Nephrology / Issue 1/2013
Print ISSN: 1342-1751
Electronic ISSN: 1437-7799
DOI
https://doi.org/10.1007/s10157-012-0709-0

Other articles of this Issue 1/2013

Clinical and Experimental Nephrology 1/2013 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.