Literature DB >> 14703948

Review of acarbose therapeutic strategies in the long-term treatment and in the prevention of type 2 diabetes.

H W M Breuer1.   

Abstract

Acarbose--the most extensively investigated and widely prescribed alpha-glucosidase inhibitor--reduces postprandial plasma glucose excursions by delaying the absorption of carbohydrate from the small intestine. Acarbose is an effective first-line therapy for patients with newly diagnosed type 2 diabetes, and induces a further improvement in glycemic control when used in combination with other antidiabetes agents. By decreasing postprandial hyperglycemia and improving insulin sensitivity, acarbose therapy also reduces fasting and postprandial serum insulin, fasting plasma glucose, and hemoglobin A1c levels. As the burden of type 2 diabetes continues to grow, there is a great need for an oral antidiabetes agent with a proven ability to prevent the development of micro- and macrovascular complications, and maintain long-term glycemic control. More than 15 years of clinical investigation have confirmed the sustained efficacy, tolerability, and excellent safety profile of acarbose in a wide range of patient types. Furthermore, the results of the recent Study to Prevent Non-Insulin-Dependent Diabetes Mellitus (STOP-NIDDM) showed that acarbose therapy significantly decreased the risk of cardiovascular events in high-risk individuals with glucose intolerance. Acarbose is therefore a convenient and effective long-term option for the treatment of type 2 diabetes, with the added benefit of reducing cardiovascular risk.

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Year:  2003        PMID: 14703948     DOI: 10.5414/cpp41421

Source DB:  PubMed          Journal:  Int J Clin Pharmacol Ther        ISSN: 0946-1965            Impact factor:   1.366


  12 in total

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Authors:  Jihene Ben Lamine; Mouhamed Ali Boujbiha; Sabra Dahane; Amal Ben Cherifa; Aida Khlifi; Hassiba Chahdoura; Mouhamed Taher Yakoubi; Salima Ferchichi; Nacer El Ayeb; Lotfi Achour
Journal:  Environ Sci Pollut Res Int       Date:  2019-02-07       Impact factor: 4.223

3.  The effect of electrostatic interactions on conformational equilibria of multiply substituted tetrahydropyran oxocarbenium ions.

Authors:  Michael T Yang; K A Woerpel
Journal:  J Org Chem       Date:  2009-01-16       Impact factor: 4.354

4.  Safety and tolerability of acarbose in the treatment of type 1 and type 2 diabetes mellitus.

Authors:  Dieter Neuser; Alice Benson; Andreas Brückner; Ronald B Goldberg; Byron J Hoogwerf; Dieter Petzinna
Journal:  Clin Drug Investig       Date:  2005       Impact factor: 2.859

5.  Evaluation of the efficacy and tolerability of acarbose in patients with diabetes mellitus : a postmarketing surveillance study.

Authors:  M Spengler; H Schmitz; H Landen
Journal:  Clin Drug Investig       Date:  2005       Impact factor: 2.859

6.  Long-term efficacy and tolerability of acarbose treatment in patients with type 2 diabetes mellitus.

Authors:  Pesach Segal; Haskel E Eliahou; Dieter Petzinna; Dieter Neuser; Andreas Brückner; Manfred Spengler
Journal:  Clin Drug Investig       Date:  2005       Impact factor: 2.859

7.  Targeting prandial hyperglycemia: how important is it and how best to do this?

Authors:  Louis Monnier; Claude Colette
Journal:  Curr Diab Rep       Date:  2008-10       Impact factor: 4.810

Review 8.  Should postprandial hyperglycaemia in prediabetic and type 2 diabetic patients be treated?

Authors:  Guillaume Charpentier; Jean-Pierre Riveline; Dured Dardari; Michel Varroud-Vial
Journal:  Drugs       Date:  2006       Impact factor: 9.546

9.  Post-marketing surveillance of acarbose treatment in patients with type 2 diabetes mellitus and subjects with impaired glucose tolerance in China.

Authors:  Chang-Yu Pan; Harald Landen
Journal:  Clin Drug Investig       Date:  2007       Impact factor: 2.859

10.  Concomitant intake of quercetin with a grain-based diet acutely lowers postprandial plasma glucose and lipid concentrations in pigs.

Authors:  Silvia Wein; Siegfried Wolffram
Journal:  Biomed Res Int       Date:  2014-04-16       Impact factor: 3.411

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