Cargando…
Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study
INTRODUCTION: Epicardial fat (EF) was reported to be independently associated with cardiovascular disease regardless of obesity. We have previously reported that a sodium-glucose co-transporter-2 (SGLT2) inhibitor, luseogliflozin, reduces the EF volume (EFV) in parallel with the reduction of body we...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544615/ https://www.ncbi.nlm.nih.gov/pubmed/28616806 http://dx.doi.org/10.1007/s13300-017-0279-y |
_version_ | 1783255273953034240 |
---|---|
author | Fukuda, Tatsuya Bouchi, Ryotaro Terashima, Masahiro Sasahara, Yuriko Asakawa, Masahiro Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro |
author_facet | Fukuda, Tatsuya Bouchi, Ryotaro Terashima, Masahiro Sasahara, Yuriko Asakawa, Masahiro Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro |
author_sort | Fukuda, Tatsuya |
collection | PubMed |
description | INTRODUCTION: Epicardial fat (EF) was reported to be independently associated with cardiovascular disease regardless of obesity. We have previously reported that a sodium-glucose co-transporter-2 (SGLT2) inhibitor, luseogliflozin, reduces the EF volume (EFV) in parallel with the reduction of body weight in obese patients (BMI ≥25 kg/m(2)) with type 2 diabetes. However, it is unknown whether SGLT2 inhibitors could reduce EFV in non-obese patients (BMI <25 kg/m(2)) with type 2 diabetes. Therefore, we evaluated the effect of SGLT2 inhibitors on the EFV in non-obese type 2 diabetic patients with visceral obesity in this pilot study. METHODS: Nine of type 2 diabetic patients (mean age 66 ± 8 years; 33% female) with HbA(1c) 6.5–9.0%, body mass index (BMI, kg/m(2)) <25.0, and visceral fat area (VFA, cm(2)) ≥100 were enrolled. Participants were administered ipragliflozin 50 mg daily. EFV [median (interquartile range), cm(3)] was measured by magnetic resonance imaging. Primary endpoint was the change in EFV at 12 weeks. VFA and liver attenuation index (LAI), skeletal muscle index (SMI), and body fat (%) were also assessed at baseline and at 12 weeks. RESULTS: The EFV was significantly reduced from 102 (79–126) cm(3) to 89 (66–109) cm(3) by ipraglifrozin (p = 0.008). The body weight, BMI, HbA(1c), fasting plasma glucose, insulin, homeostasis model assessment-insulin resistance, triglycerides, leptin, body fat, android, gynoid, and VFA were significantly reduced and high-density lipoprotein cholesterol was significantly increased by ipraglifrozin at 12 weeks, whereas SFA and LAI were unchanged. The change in EFV was significantly correlated with the change in BMI. CONCLUSIONS: A12-week intervention of ipragliflozin reduced the EFV in non-obese type 2 diabetic patients with visceral adiposity. CLINICAL TRIAL REGISTRATION: UMIN Clinical Trial Registry: UMIN000019071. FUNDING: Astellas Pharma Inc. and the Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan. |
format | Online Article Text |
id | pubmed-5544615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-55446152017-08-18 Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study Fukuda, Tatsuya Bouchi, Ryotaro Terashima, Masahiro Sasahara, Yuriko Asakawa, Masahiro Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro Diabetes Ther Original Research INTRODUCTION: Epicardial fat (EF) was reported to be independently associated with cardiovascular disease regardless of obesity. We have previously reported that a sodium-glucose co-transporter-2 (SGLT2) inhibitor, luseogliflozin, reduces the EF volume (EFV) in parallel with the reduction of body weight in obese patients (BMI ≥25 kg/m(2)) with type 2 diabetes. However, it is unknown whether SGLT2 inhibitors could reduce EFV in non-obese patients (BMI <25 kg/m(2)) with type 2 diabetes. Therefore, we evaluated the effect of SGLT2 inhibitors on the EFV in non-obese type 2 diabetic patients with visceral obesity in this pilot study. METHODS: Nine of type 2 diabetic patients (mean age 66 ± 8 years; 33% female) with HbA(1c) 6.5–9.0%, body mass index (BMI, kg/m(2)) <25.0, and visceral fat area (VFA, cm(2)) ≥100 were enrolled. Participants were administered ipragliflozin 50 mg daily. EFV [median (interquartile range), cm(3)] was measured by magnetic resonance imaging. Primary endpoint was the change in EFV at 12 weeks. VFA and liver attenuation index (LAI), skeletal muscle index (SMI), and body fat (%) were also assessed at baseline and at 12 weeks. RESULTS: The EFV was significantly reduced from 102 (79–126) cm(3) to 89 (66–109) cm(3) by ipraglifrozin (p = 0.008). The body weight, BMI, HbA(1c), fasting plasma glucose, insulin, homeostasis model assessment-insulin resistance, triglycerides, leptin, body fat, android, gynoid, and VFA were significantly reduced and high-density lipoprotein cholesterol was significantly increased by ipraglifrozin at 12 weeks, whereas SFA and LAI were unchanged. The change in EFV was significantly correlated with the change in BMI. CONCLUSIONS: A12-week intervention of ipragliflozin reduced the EFV in non-obese type 2 diabetic patients with visceral adiposity. CLINICAL TRIAL REGISTRATION: UMIN Clinical Trial Registry: UMIN000019071. FUNDING: Astellas Pharma Inc. and the Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan. Springer Healthcare 2017-06-14 2017-08 /pmc/articles/PMC5544615/ /pubmed/28616806 http://dx.doi.org/10.1007/s13300-017-0279-y Text en © The Author(s) 2017 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial 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. |
spellingShingle | Original Research Fukuda, Tatsuya Bouchi, Ryotaro Terashima, Masahiro Sasahara, Yuriko Asakawa, Masahiro Takeuchi, Takato Nakano, Yujiro Murakami, Masanori Minami, Isao Izumiyama, Hajime Hashimoto, Koshi Yoshimoto, Takanobu Ogawa, Yoshihiro Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study |
title | Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study |
title_full | Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study |
title_fullStr | Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study |
title_full_unstemmed | Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study |
title_short | Ipragliflozin Reduces Epicardial Fat Accumulation in Non-Obese Type 2 Diabetic Patients with Visceral Obesity: A Pilot Study |
title_sort | ipragliflozin reduces epicardial fat accumulation in non-obese type 2 diabetic patients with visceral obesity: a pilot study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5544615/ https://www.ncbi.nlm.nih.gov/pubmed/28616806 http://dx.doi.org/10.1007/s13300-017-0279-y |
work_keys_str_mv | AT fukudatatsuya ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT bouchiryotaro ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT terashimamasahiro ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT sasaharayuriko ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT asakawamasahiro ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT takeuchitakato ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT nakanoyujiro ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT murakamimasanori ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT minamiisao ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT izumiyamahajime ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT hashimotokoshi ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT yoshimototakanobu ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy AT ogawayoshihiro ipragliflozinreducesepicardialfataccumulationinnonobesetype2diabeticpatientswithvisceralobesityapilotstudy |