Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus

Abstract Background It is unknown whether canagliflozin, a selective sodium glucose co-transporter 2 inhibitor, reduces epicardial adipose tissue (EAT) thickness, which is associated with insulin resistance and is a risk factor for coronary artery disease. Methods and results We administered 100 mg...

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Main Authors: Shusuke Yagi, Yukina Hirata, Takayuki Ise, Kenya Kusunose, Hirotsugu Yamada, Daiju Fukuda, Hotimah Masdan Salim, Gulinu Maimaituxun, Susumu Nishio, Yuriko Takagawa, Saori Hama, Tomomi Matsuura, Koji Yamaguchi, Takeshi Tobiume, Takeshi Soeki, Tetsuzo Wakatsuki, Ken-ichi Aihara, Masashi Akaike, Michio Shimabukuro, Masataka Sata
Format: Article
Language:English
Published: BMC 2017-10-01
Series:Diabetology & Metabolic Syndrome
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13098-017-0275-4
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author Shusuke Yagi
Yukina Hirata
Takayuki Ise
Kenya Kusunose
Hirotsugu Yamada
Daiju Fukuda
Hotimah Masdan Salim
Gulinu Maimaituxun
Susumu Nishio
Yuriko Takagawa
Saori Hama
Tomomi Matsuura
Koji Yamaguchi
Takeshi Tobiume
Takeshi Soeki
Tetsuzo Wakatsuki
Ken-ichi Aihara
Masashi Akaike
Michio Shimabukuro
Masataka Sata
author_facet Shusuke Yagi
Yukina Hirata
Takayuki Ise
Kenya Kusunose
Hirotsugu Yamada
Daiju Fukuda
Hotimah Masdan Salim
Gulinu Maimaituxun
Susumu Nishio
Yuriko Takagawa
Saori Hama
Tomomi Matsuura
Koji Yamaguchi
Takeshi Tobiume
Takeshi Soeki
Tetsuzo Wakatsuki
Ken-ichi Aihara
Masashi Akaike
Michio Shimabukuro
Masataka Sata
author_sort Shusuke Yagi
collection DOAJ
description Abstract Background It is unknown whether canagliflozin, a selective sodium glucose co-transporter 2 inhibitor, reduces epicardial adipose tissue (EAT) thickness, which is associated with insulin resistance and is a risk factor for coronary artery disease. Methods and results We administered 100 mg of canagliflozin for 6 months to 13 patients with type 2 diabetes mellitus. We evaluated glycemic control, visceral adipose tissue (VAT) area and subcutaneous adipose tissue (SAT) area, and skeletal muscle mass by using impedance methods, and EAT thickness by using echocardiography. Canagliflozin treatment for 6 months decreased hemoglobin A1c level from 7.1 ± 0.5% to 6.7 ± 0.6% (P < 0.05) and decreased EAT thickness from 9.3 ± 2.5 to 7.3 ± 2.0 mm (P < 0.001), along with a trend of decreasing VAT and SAT area. No association was found between any of these changes. Conclusion Canagliflozin reduced EAT thickness in patients with type 2 diabetes mellitus independent of its effect on lowering blood glucose, suggesting that canagliflozin may have an effect in preventing cardiovascular events in these patients (UMIN000021327).
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spelling doaj.art-8e5336d81f7b48f3b467a8270bef0d682022-12-21T23:46:57ZengBMCDiabetology & Metabolic Syndrome1758-59962017-10-01911710.1186/s13098-017-0275-4Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitusShusuke Yagi0Yukina Hirata1Takayuki Ise2Kenya Kusunose3Hirotsugu Yamada4Daiju Fukuda5Hotimah Masdan Salim6Gulinu Maimaituxun7Susumu Nishio8Yuriko Takagawa9Saori Hama10Tomomi Matsuura11Koji Yamaguchi12Takeshi Tobiume13Takeshi Soeki14Tetsuzo Wakatsuki15Ken-ichi Aihara16Masashi Akaike17Michio Shimabukuro18Masataka Sata19Department of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesUltrasound Examination Center, Tokushima University HospitalDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesUltrasound Examination Center, Tokushima University HospitalDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Community Medicine for Diabetes and Metabolic Disorders, Tokushima University Graduate School of Biomedical SciencesDepartment of Medical Education, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardio-Diabetes Medicine, Tokushima University Graduate School of Biomedical SciencesDepartment of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical SciencesAbstract Background It is unknown whether canagliflozin, a selective sodium glucose co-transporter 2 inhibitor, reduces epicardial adipose tissue (EAT) thickness, which is associated with insulin resistance and is a risk factor for coronary artery disease. Methods and results We administered 100 mg of canagliflozin for 6 months to 13 patients with type 2 diabetes mellitus. We evaluated glycemic control, visceral adipose tissue (VAT) area and subcutaneous adipose tissue (SAT) area, and skeletal muscle mass by using impedance methods, and EAT thickness by using echocardiography. Canagliflozin treatment for 6 months decreased hemoglobin A1c level from 7.1 ± 0.5% to 6.7 ± 0.6% (P < 0.05) and decreased EAT thickness from 9.3 ± 2.5 to 7.3 ± 2.0 mm (P < 0.001), along with a trend of decreasing VAT and SAT area. No association was found between any of these changes. Conclusion Canagliflozin reduced EAT thickness in patients with type 2 diabetes mellitus independent of its effect on lowering blood glucose, suggesting that canagliflozin may have an effect in preventing cardiovascular events in these patients (UMIN000021327).http://link.springer.com/article/10.1186/s13098-017-0275-4Epicardial adipose tissueSGLT2 inhibitorsEchocardiography
spellingShingle Shusuke Yagi
Yukina Hirata
Takayuki Ise
Kenya Kusunose
Hirotsugu Yamada
Daiju Fukuda
Hotimah Masdan Salim
Gulinu Maimaituxun
Susumu Nishio
Yuriko Takagawa
Saori Hama
Tomomi Matsuura
Koji Yamaguchi
Takeshi Tobiume
Takeshi Soeki
Tetsuzo Wakatsuki
Ken-ichi Aihara
Masashi Akaike
Michio Shimabukuro
Masataka Sata
Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
Diabetology & Metabolic Syndrome
Epicardial adipose tissue
SGLT2 inhibitors
Echocardiography
title Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
title_full Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
title_fullStr Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
title_full_unstemmed Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
title_short Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
title_sort canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
topic Epicardial adipose tissue
SGLT2 inhibitors
Echocardiography
url http://link.springer.com/article/10.1186/s13098-017-0275-4
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