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Canagliflozin for Japanese patients with chronic heart failure and type II diabetes

BACKGROUND: Reports that sodium glucose cotransporter 2 inhibitors decrease cardiovascular death and events in patients with diabetes have attracted attention in the cardiology field. We conducted a study of canagliflozin in patients with chronic heart failure and type II diabetes. METHODS: Thirty-f...

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Autores principales: Sezai, Akira, Sekino, Hisakuni, Unosawa, Satoshi, Taoka, Makoto, Osaka, Shunji, Tanaka, Masashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551875/
https://www.ncbi.nlm.nih.gov/pubmed/31167663
http://dx.doi.org/10.1186/s12933-019-0877-2
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author Sezai, Akira
Sekino, Hisakuni
Unosawa, Satoshi
Taoka, Makoto
Osaka, Shunji
Tanaka, Masashi
author_facet Sezai, Akira
Sekino, Hisakuni
Unosawa, Satoshi
Taoka, Makoto
Osaka, Shunji
Tanaka, Masashi
author_sort Sezai, Akira
collection PubMed
description BACKGROUND: Reports that sodium glucose cotransporter 2 inhibitors decrease cardiovascular death and events in patients with diabetes have attracted attention in the cardiology field. We conducted a study of canagliflozin in patients with chronic heart failure and type II diabetes. METHODS: Thirty-five Japanese patients with chronic heart failure and type II diabetes were treated with canagliflozin for 12 months. The primary endpoints were the changes of subcutaneous, visceral, and total fat areas at 12 months determined by computed tomography. Secondary endpoints included markers of glycemic control, renal function, and oxidative stress, as well as lipid parameters, atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), flow-mediated dilation (FMD), and echocardiographic left ventricular function. RESULTS: All fat areas (subcutaneous, visceral, and total) showed a significant decrease at 12 months. ANP and BNP also decreased significantly, along with improvement of renal function, oxidized LDL, and E/e′, FMD increased significantly after canagliflozin treatment. CONCLUSION: Canagliflozin demonstrated cardiac and renal protective effects as well as improving oxidative stress, diastolic function, and endothelial function. This drug was effective in patients who had heart failure with preserved ejection fraction and could become first-line therapy for such patients with diabetes. Trial registration UMIN (http://www.umin.ac.jp/), Study ID: UMIN000021239
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spelling pubmed-65518752019-06-07 Canagliflozin for Japanese patients with chronic heart failure and type II diabetes Sezai, Akira Sekino, Hisakuni Unosawa, Satoshi Taoka, Makoto Osaka, Shunji Tanaka, Masashi Cardiovasc Diabetol Original Investigation BACKGROUND: Reports that sodium glucose cotransporter 2 inhibitors decrease cardiovascular death and events in patients with diabetes have attracted attention in the cardiology field. We conducted a study of canagliflozin in patients with chronic heart failure and type II diabetes. METHODS: Thirty-five Japanese patients with chronic heart failure and type II diabetes were treated with canagliflozin for 12 months. The primary endpoints were the changes of subcutaneous, visceral, and total fat areas at 12 months determined by computed tomography. Secondary endpoints included markers of glycemic control, renal function, and oxidative stress, as well as lipid parameters, atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), flow-mediated dilation (FMD), and echocardiographic left ventricular function. RESULTS: All fat areas (subcutaneous, visceral, and total) showed a significant decrease at 12 months. ANP and BNP also decreased significantly, along with improvement of renal function, oxidized LDL, and E/e′, FMD increased significantly after canagliflozin treatment. CONCLUSION: Canagliflozin demonstrated cardiac and renal protective effects as well as improving oxidative stress, diastolic function, and endothelial function. This drug was effective in patients who had heart failure with preserved ejection fraction and could become first-line therapy for such patients with diabetes. Trial registration UMIN (http://www.umin.ac.jp/), Study ID: UMIN000021239 BioMed Central 2019-06-05 /pmc/articles/PMC6551875/ /pubmed/31167663 http://dx.doi.org/10.1186/s12933-019-0877-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Sezai, Akira
Sekino, Hisakuni
Unosawa, Satoshi
Taoka, Makoto
Osaka, Shunji
Tanaka, Masashi
Canagliflozin for Japanese patients with chronic heart failure and type II diabetes
title Canagliflozin for Japanese patients with chronic heart failure and type II diabetes
title_full Canagliflozin for Japanese patients with chronic heart failure and type II diabetes
title_fullStr Canagliflozin for Japanese patients with chronic heart failure and type II diabetes
title_full_unstemmed Canagliflozin for Japanese patients with chronic heart failure and type II diabetes
title_short Canagliflozin for Japanese patients with chronic heart failure and type II diabetes
title_sort canagliflozin for japanese patients with chronic heart failure and type ii diabetes
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551875/
https://www.ncbi.nlm.nih.gov/pubmed/31167663
http://dx.doi.org/10.1186/s12933-019-0877-2
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