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Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin

Insulin resistance and impaired beta-cell function are primary defects that occur early in the course of development of type 2 diabetes. Insulin resistance leads to hyperinsulinemia in order to maintain normal glucose tolerance. In most cases of type 2 diabetes, beta-cell dysfunction develops subseq...

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Detalles Bibliográficos
Autor principal: Schwartz, Stanley S
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3047993/
https://www.ncbi.nlm.nih.gov/pubmed/21437092
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author Schwartz, Stanley S
author_facet Schwartz, Stanley S
author_sort Schwartz, Stanley S
collection PubMed
description Insulin resistance and impaired beta-cell function are primary defects that occur early in the course of development of type 2 diabetes. Insulin resistance leads to hyperinsulinemia in order to maintain normal glucose tolerance. In most cases of type 2 diabetes, beta-cell dysfunction develops subsequent to the development of insulin resistance, and it is not until such beta-cell dysfunction develops that any abnormality in glucose tolerance is seen. Insulin resistance is a primary defect in type 2 diabetes. The risk of coronary heart disease is significantly increased in patients with type 2 diabetes. Cardiovascular disease causes 80% of all diabetic mortality, and in 75% of those cases, it is a result of coronary atherosclerosis. These points provide a rationale for early and aggressive management of cardiovascular risk in patients with diabetes. Thiazolidinediones represent an effective tool for targeting some features of this increased risk as they decrease insulin resistance and can prevent and/or delay diabetes progression.
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spelling pubmed-30479932011-03-23 Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin Schwartz, Stanley S Diabetes Metab Syndr Obes Review Insulin resistance and impaired beta-cell function are primary defects that occur early in the course of development of type 2 diabetes. Insulin resistance leads to hyperinsulinemia in order to maintain normal glucose tolerance. In most cases of type 2 diabetes, beta-cell dysfunction develops subsequent to the development of insulin resistance, and it is not until such beta-cell dysfunction develops that any abnormality in glucose tolerance is seen. Insulin resistance is a primary defect in type 2 diabetes. The risk of coronary heart disease is significantly increased in patients with type 2 diabetes. Cardiovascular disease causes 80% of all diabetic mortality, and in 75% of those cases, it is a result of coronary atherosclerosis. These points provide a rationale for early and aggressive management of cardiovascular risk in patients with diabetes. Thiazolidinediones represent an effective tool for targeting some features of this increased risk as they decrease insulin resistance and can prevent and/or delay diabetes progression. Dove Medical Press 2010-07-09 /pmc/articles/PMC3047993/ /pubmed/21437092 Text en © 2010 Schwartz, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Schwartz, Stanley S
Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin
title Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin
title_full Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin
title_fullStr Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin
title_full_unstemmed Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin
title_short Pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin
title_sort pioglitazone for the treatment of type 2 diabetes in patients inadequately controlled on insulin
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3047993/
https://www.ncbi.nlm.nih.gov/pubmed/21437092
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