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Optimizing combination treatment in the management of type 2 diabetes

Obtaining the suggested glycemic control is the most important achievement in order to prevent cardiovascular complications in patients with type 2 diabetes. Monotherapy often fails after a period of treatment, so that multiple drugs are needed to achieve effective glycemic control. A number of oral...

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Detalles Bibliográficos
Autores principales: Derosa, Giuseppe, Sibilla, Salvadeo
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291311/
https://www.ncbi.nlm.nih.gov/pubmed/18078018
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author Derosa, Giuseppe
Sibilla, Salvadeo
author_facet Derosa, Giuseppe
Sibilla, Salvadeo
author_sort Derosa, Giuseppe
collection PubMed
description Obtaining the suggested glycemic control is the most important achievement in order to prevent cardiovascular complications in patients with type 2 diabetes. Monotherapy often fails after a period of treatment, so that multiple drugs are needed to achieve effective glycemic control. A number of oral glucose lowering drugs is now available such as metformin, sulfonylureas, non-sulfonylureas secretagogues (metiglinides derivatives), alpha-glucosidases inhibitors, and the newest agent: thiazolidinediones (TZD). The possible associations of oral glucose lowering drugs for optimal treatment of type 2 diabetes are briefly reviewed. In particular, the effects of different classes of drugs on cardiovascular risk factors (and particular hypertension and dyslipidemia) and well recognized cardiovascular disease markers in type 2 diabetes are analyzed: in this context TZD appear the more innovative drugs and have been shown to play a key role in the management of hypertension, dyslipidemia, inflammation and endothelial disfunction in diabetic patients. The possible adverse effects derived from the association of different drug classes are also considered.
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spelling pubmed-22913112008-04-22 Optimizing combination treatment in the management of type 2 diabetes Derosa, Giuseppe Sibilla, Salvadeo Vasc Health Risk Manag Review Obtaining the suggested glycemic control is the most important achievement in order to prevent cardiovascular complications in patients with type 2 diabetes. Monotherapy often fails after a period of treatment, so that multiple drugs are needed to achieve effective glycemic control. A number of oral glucose lowering drugs is now available such as metformin, sulfonylureas, non-sulfonylureas secretagogues (metiglinides derivatives), alpha-glucosidases inhibitors, and the newest agent: thiazolidinediones (TZD). The possible associations of oral glucose lowering drugs for optimal treatment of type 2 diabetes are briefly reviewed. In particular, the effects of different classes of drugs on cardiovascular risk factors (and particular hypertension and dyslipidemia) and well recognized cardiovascular disease markers in type 2 diabetes are analyzed: in this context TZD appear the more innovative drugs and have been shown to play a key role in the management of hypertension, dyslipidemia, inflammation and endothelial disfunction in diabetic patients. The possible adverse effects derived from the association of different drug classes are also considered. Dove Medical Press 2007-10 /pmc/articles/PMC2291311/ /pubmed/18078018 Text en © 2007 Dove Medical Press Limited. All rights reserved
spellingShingle Review
Derosa, Giuseppe
Sibilla, Salvadeo
Optimizing combination treatment in the management of type 2 diabetes
title Optimizing combination treatment in the management of type 2 diabetes
title_full Optimizing combination treatment in the management of type 2 diabetes
title_fullStr Optimizing combination treatment in the management of type 2 diabetes
title_full_unstemmed Optimizing combination treatment in the management of type 2 diabetes
title_short Optimizing combination treatment in the management of type 2 diabetes
title_sort optimizing combination treatment in the management of type 2 diabetes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291311/
https://www.ncbi.nlm.nih.gov/pubmed/18078018
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