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Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers

Although the use of β-blockers may help in achieving maximum effects of intensive glycemic control because of a decrease in the adverse effects after severe hypoglycemia, they pose a potential risk for the occurrence of severe hypoglycemia. This study aimed to evaluate whether the use of β-blockers...

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Autores principales: Tsujimoto, Tetsuro, Sugiyama, Takehiro, Shapiro, Martin F., Noda, Mitsuhiko, Kajio, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott, Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739105/
https://www.ncbi.nlm.nih.gov/pubmed/28559400
http://dx.doi.org/10.1161/HYPERTENSIONAHA.117.09259
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author Tsujimoto, Tetsuro
Sugiyama, Takehiro
Shapiro, Martin F.
Noda, Mitsuhiko
Kajio, Hiroshi
author_facet Tsujimoto, Tetsuro
Sugiyama, Takehiro
Shapiro, Martin F.
Noda, Mitsuhiko
Kajio, Hiroshi
author_sort Tsujimoto, Tetsuro
collection PubMed
description Although the use of β-blockers may help in achieving maximum effects of intensive glycemic control because of a decrease in the adverse effects after severe hypoglycemia, they pose a potential risk for the occurrence of severe hypoglycemia. This study aimed to evaluate whether the use of β-blockers is effective in patients with diabetes mellitus and whether its use is associated with the occurrence of severe hypoglycemia. Using the ACCORD trial (Action to Control Cardiovascular Risk in Diabetes) data, we performed Cox proportional hazards analyses with a propensity score adjustment. The primary outcome was the first occurrence of a cardiovascular event during the study period, which included nonfatal myocardial infarction, unstable angina, nonfatal stroke, and cardiovascular death. The mean follow-up periods (±SD) were 4.6±1.6 years in patients on β-blockers (n=2527) and 4.7±1.6 years in those not on β-blockers (n=2527). The cardiovascular event rate was significantly higher in patients on β-blockers than in those not on β-blockers (hazard ratio, 1.46; 95% confidence interval, 1.24–1.72; P<0.001). In patients with coronary heart disease or heart failure, the cumulative event rate for cardiovascular events was also significantly higher in those on β-blockers than in those not on β-blockers (hazard ratio, 1.27; 95% confidence interval, 1.02–1.60; P=0.03). The incidence of severe hypoglycemia was significantly higher in patients on β-blockers than in those not on β-blockers (hazard ratio, 1.30; 95% confidence interval, 1.03–1.64; P=0.02). In conclusion, the use of β-blockers in patients with diabetes mellitus was associated with an increased risk for cardiovascular events.
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spelling pubmed-57391052018-01-12 Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers Tsujimoto, Tetsuro Sugiyama, Takehiro Shapiro, Martin F. Noda, Mitsuhiko Kajio, Hiroshi Hypertension Original Articles Although the use of β-blockers may help in achieving maximum effects of intensive glycemic control because of a decrease in the adverse effects after severe hypoglycemia, they pose a potential risk for the occurrence of severe hypoglycemia. This study aimed to evaluate whether the use of β-blockers is effective in patients with diabetes mellitus and whether its use is associated with the occurrence of severe hypoglycemia. Using the ACCORD trial (Action to Control Cardiovascular Risk in Diabetes) data, we performed Cox proportional hazards analyses with a propensity score adjustment. The primary outcome was the first occurrence of a cardiovascular event during the study period, which included nonfatal myocardial infarction, unstable angina, nonfatal stroke, and cardiovascular death. The mean follow-up periods (±SD) were 4.6±1.6 years in patients on β-blockers (n=2527) and 4.7±1.6 years in those not on β-blockers (n=2527). The cardiovascular event rate was significantly higher in patients on β-blockers than in those not on β-blockers (hazard ratio, 1.46; 95% confidence interval, 1.24–1.72; P<0.001). In patients with coronary heart disease or heart failure, the cumulative event rate for cardiovascular events was also significantly higher in those on β-blockers than in those not on β-blockers (hazard ratio, 1.27; 95% confidence interval, 1.02–1.60; P=0.03). The incidence of severe hypoglycemia was significantly higher in patients on β-blockers than in those not on β-blockers (hazard ratio, 1.30; 95% confidence interval, 1.03–1.64; P=0.02). In conclusion, the use of β-blockers in patients with diabetes mellitus was associated with an increased risk for cardiovascular events. Lippincott, Williams & Wilkins 2017-07 2017-05-15 /pmc/articles/PMC5739105/ /pubmed/28559400 http://dx.doi.org/10.1161/HYPERTENSIONAHA.117.09259 Text en © 2017 The Authors. Hypertension is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Original Articles
Tsujimoto, Tetsuro
Sugiyama, Takehiro
Shapiro, Martin F.
Noda, Mitsuhiko
Kajio, Hiroshi
Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers
title Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers
title_full Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers
title_fullStr Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers
title_full_unstemmed Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers
title_short Risk of Cardiovascular Events in Patients With Diabetes Mellitus on β-Blockers
title_sort risk of cardiovascular events in patients with diabetes mellitus on β-blockers
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739105/
https://www.ncbi.nlm.nih.gov/pubmed/28559400
http://dx.doi.org/10.1161/HYPERTENSIONAHA.117.09259
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