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Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study

OBJECTIVE: Several large clinical trials suggest that ACE inhibitors may reduce the incidence of diabetes. Less is known about the effects of angiotensin receptor blockers (ARBs) on reducing incident diabetes or leading to regression of impaired fasting glucose (IFG) or impaired glucose tolerance (I...

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Autores principales: Barzilay, Joshua I., Gao, Peggy, Rydén, Lars, Schumacher, Helmut, Probstfield, Jeffrey, Commerford, Patrick, Dans, Antonio, Ferreira, Rafael, Keltai, Mátyás, Paolasso, Ernesto, Yusuf, Salim, Teo, Koon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161302/
https://www.ncbi.nlm.nih.gov/pubmed/21788624
http://dx.doi.org/10.2337/dc11-0545
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author Barzilay, Joshua I.
Gao, Peggy
Rydén, Lars
Schumacher, Helmut
Probstfield, Jeffrey
Commerford, Patrick
Dans, Antonio
Ferreira, Rafael
Keltai, Mátyás
Paolasso, Ernesto
Yusuf, Salim
Teo, Koon
author_facet Barzilay, Joshua I.
Gao, Peggy
Rydén, Lars
Schumacher, Helmut
Probstfield, Jeffrey
Commerford, Patrick
Dans, Antonio
Ferreira, Rafael
Keltai, Mátyás
Paolasso, Ernesto
Yusuf, Salim
Teo, Koon
author_sort Barzilay, Joshua I.
collection PubMed
description OBJECTIVE: Several large clinical trials suggest that ACE inhibitors may reduce the incidence of diabetes. Less is known about the effects of angiotensin receptor blockers (ARBs) on reducing incident diabetes or leading to regression of impaired fasting glucose (IFG) or impaired glucose tolerance (IGT) to normoglycemia. RESEARCH DESIGN AND METHODS: Participants were 3,488 adults at high risk for cardiovascular disease but free from diabetes (mean age 67 years; 61% male) in the Telmisartan Randomized Assessment Study in ACE Intolerant Subjects With Cardiovascular Disease (TRANSCEND) study. The participants were randomized to the ARB telmisartan 80 mg (n = 1,726) or placebo (n = 1,762) in addition to usual care. RESULTS: During a median 56 months, 21.8% of participants treated with telmisartan and 22.4% of those on placebo developed diabetes (relative ratio 0.95 [95% CI 0.83–1.10]; P = 0.51). Participants originally diagnosed with IFG and/or IGT were equally likely to regress to normoglycemia (26.9 vs. 24.5%) or to progress to incident diabetes (20.1 vs. 21.1%; P = 0.59) on telmisartan or placebo. CONCLUSIONS: There was no evidence that addition of the ARB telmisartan to usual care prevents incident diabetes or leads to regression of IFG or IGT in people at high risk for cardiovascular disease but free from diabetes.
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spelling pubmed-31613022012-09-01 Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study Barzilay, Joshua I. Gao, Peggy Rydén, Lars Schumacher, Helmut Probstfield, Jeffrey Commerford, Patrick Dans, Antonio Ferreira, Rafael Keltai, Mátyás Paolasso, Ernesto Yusuf, Salim Teo, Koon Diabetes Care Original Research OBJECTIVE: Several large clinical trials suggest that ACE inhibitors may reduce the incidence of diabetes. Less is known about the effects of angiotensin receptor blockers (ARBs) on reducing incident diabetes or leading to regression of impaired fasting glucose (IFG) or impaired glucose tolerance (IGT) to normoglycemia. RESEARCH DESIGN AND METHODS: Participants were 3,488 adults at high risk for cardiovascular disease but free from diabetes (mean age 67 years; 61% male) in the Telmisartan Randomized Assessment Study in ACE Intolerant Subjects With Cardiovascular Disease (TRANSCEND) study. The participants were randomized to the ARB telmisartan 80 mg (n = 1,726) or placebo (n = 1,762) in addition to usual care. RESULTS: During a median 56 months, 21.8% of participants treated with telmisartan and 22.4% of those on placebo developed diabetes (relative ratio 0.95 [95% CI 0.83–1.10]; P = 0.51). Participants originally diagnosed with IFG and/or IGT were equally likely to regress to normoglycemia (26.9 vs. 24.5%) or to progress to incident diabetes (20.1 vs. 21.1%; P = 0.59) on telmisartan or placebo. CONCLUSIONS: There was no evidence that addition of the ARB telmisartan to usual care prevents incident diabetes or leads to regression of IFG or IGT in people at high risk for cardiovascular disease but free from diabetes. American Diabetes Association 2011-09 2011-08-19 /pmc/articles/PMC3161302/ /pubmed/21788624 http://dx.doi.org/10.2337/dc11-0545 Text en © 2011 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Barzilay, Joshua I.
Gao, Peggy
Rydén, Lars
Schumacher, Helmut
Probstfield, Jeffrey
Commerford, Patrick
Dans, Antonio
Ferreira, Rafael
Keltai, Mátyás
Paolasso, Ernesto
Yusuf, Salim
Teo, Koon
Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study
title Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study
title_full Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study
title_fullStr Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study
title_full_unstemmed Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study
title_short Effects of Telmisartan on Glucose Levels in People at High Risk for Cardiovascular Disease but Free From Diabetes: The TRANSCEND study
title_sort effects of telmisartan on glucose levels in people at high risk for cardiovascular disease but free from diabetes: the transcend study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161302/
https://www.ncbi.nlm.nih.gov/pubmed/21788624
http://dx.doi.org/10.2337/dc11-0545
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