Abstract
Introduction: Healthy eating is a critical aspect of the prevention and management of type 2 diabetes (T2DM). Disrupted eating patterns can result in poor glucose control and increase the likelihood of diabetic complications. Teneligliptin inhibits dipeptidyl peptidase-4 activity for 24 h and suppresses postprandial hyperglycemia after all three daily meals. This interim analysis of data from the large-scale post-marketing surveillance of teneligliptin (RUBY) in Japan examined eating patterns and their relationship with metabolic parameters and diabetic complications. We also examined whether eating patterns affected safety and efficacy of teneligliptin. Methods: We analyzed baseline data from survey forms collected in RUBY between May 2013 and June 2017, including patient characteristics, metabolic parameters, and eating patterns (eating three meals per day or not; timing of evening meal) before teneligliptin treatment was initiated. Safety and efficacy of 12 months’ teneligliptin (20–40 mg/day) treatment was assessed. Results: Data from 10,532 patients were available for analysis. Most patients who did not eat three meals per day (n =757) or who ate their evening meal after 10 PM (n =206) were 64 years old or younger. At baseline, glycated hemoglobin (HbA1c), fasting blood glucose, triglycerides, total and low-density lipoprotein cholesterol, body mass index, alanine aminotransferase, and aspartate aminotransferase levels were higher in those patients who did not eat three meals per day (p < 0.05) or who ate their evening meal late (p < 0.05). Diabetic complications were more common in patients who did not eat three meals per day. Treatment with teneligliptin reduced HbA1c over 6 or 12 months across all eating patterns, with a low incidence of adverse drug reactions. Conclusions: Eating patterns may be associated with altered metabolic parameters and diabetic complications among Japanese patients with T2DM. Teneligliptin may be well tolerated and improve hyperglycemia in patients with T2DM irrespective of eating patterns. Funding: Mitsubishi Tanabe Pharma Corporation and Daiichi Sankyo Co. Ltd. Trial Registration Number: Japic CTI-153047.
Original language | English |
---|---|
Pages (from-to) | 817-831 |
Number of pages | 15 |
Journal | Advances in Therapy |
Volume | 35 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jun 1 2018 |
Keywords
- Dipeptidyl peptidase-4 inhibitor
- Eating pattern
- HbA1c
- Post-marketing surveillance
- Teneligliptin
- Type 2 diabetes
ASJC Scopus subject areas
- Pharmacology (medical)
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In: Advances in Therapy, Vol. 35, No. 6, 01.06.2018, p. 817-831.
Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Relationship of Eating Patterns and Metabolic Parameters, and Teneligliptin Treatment
T2 - Interim Results from Post-marketing Surveillance in Japanese Type 2 Diabetes Patients
AU - Kadowaki, Takashi
AU - Haneda, Masakazu
AU - Ito, Hiroshi
AU - Sasaki, Kazuyo
AU - Hiraide, Sonoe
AU - Matsukawa, Miyuki
AU - Ueno, Makoto
N1 - Funding Information: Disclosures. Takashi Kadowaki has received speaker honorarium/lecture fees from Astellas Pharma Inc., AstraZeneca K.K., Eli Lilly Japan K.K., Kowa Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd.; has received research grants from Daiichi Sankyo Co., Ltd., Novartis Pharma K.K., and Takeda Pharmaceutical Co., Ltd.; has received scholarship grants from Astellas Pharma Inc., Daiichi Sankyo Co., Ltd., Kissei Pharmaceutical Co., Ltd., Kyowa Hakko Kirin Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., Sanofi K. K., Sumitomo Dainippon Pharma Co., Ltd., Taisho Toyama Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd.; and has belonged to courses endowed by Kowa Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd. Masakazu Haneda has received speaker honorarium/lecture fees from Astellas Pharma Inc., Kowa Pharmaceutical Co., Ltd., Mitsubishi Tan-abe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novartis Pharma K.K., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., Sanofi K.K., Taisho Pharmaceutical Co., Ltd., and Taisho Toyama Pharmaceutical Co., Ltd.; and has received scholarship grants from Astellas Pharma Inc., Daiichi Sankyo Co., Ltd., Eli Lilly Japan K.K., Johnson & Johnson K.K., Kissei Pharmaceutical Co., Ltd., Kowa Pharmaceutical Co., Ltd., Kyowa Hakko Kirin Co., Ltd., Mitsubishi Tanabe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Sanofi K.K., Shionogi & Co., Ltd., Taisho Toyama Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd. Hiroshi Ito has received speaker honorarium/ lecture fees from Daiichi Sankyo Co., Ltd. and Mitsubishi Tanabe Pharma Corporation, and has received scholarship grants from Daiichi Sankyo Co., Ltd. and Mitsubishi Tanabe Pharma Corporation. Kazuyo Sasaki is an employee of the Mitsubishi Tanabe Pharma Corporation. Makoto Ueno is an employee of the Mitsubishi Tanabe Pharma Corporation. Sonoe Hiraide is an employee of the Mitsubishi Tanabe Pharma Corporation. Miyuki Matsukawa is an employee of the Mitsubishi Tanabe Pharma Corporation. Funding Information: We would like to extend our sincerest gratitude to all participants and physicians and physicians at the participating facilities. We would also like to acknowledge the contributions of Mr. K. Yoshida for survey forms collection, Ms. R. Wakamoto for data management, and Ms. T. Yamakura for insightful discussions. The RUBY surveillance program was funded by Mitsubishi Tanabe Pharma Corporation, and Daiichi Sankyo Co. Ltd. Medical writing support was funded by the Mitsubishi Tanabe Pharma Corporation, Osaka, Japan. The article processing charges and open access fee for this publication were funded by Mitsubishi Tanabe Pharma Corp. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published. Takashi Kadowaki, Masakazu Haneda, and Hiroshi Ito, all contributed to the data interpretation and provided medical advice. Kazuyo Sasaki, Makoto Ueno, and Sonoe Hiraide contributed to the conception of the surveillance and data interpretation. Miyuki Matsukawa?contributed to the analyses and data interpretation. All authors contributed to the manuscript development. Medical writing support, under the direction of the authors, was provided by Caroline Shepherd, B.Pharm. of CMC CONNECT, a division of Complete Medical Communications Ltd, Macclesfield, UK, and Janet Dawson PhD, on behalf of CMC CONNECT, funded by Mitsubishi Tanabe Pharma Corporation, in accordance with Good Publication Practice (GPP3) guidelines. Takashi Kadowaki has received speaker honorarium/lecture fees from Astellas Pharma Inc., AstraZeneca K.K., Eli Lilly Japan K.K., Kowa Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd.; has received research grants from Daiichi Sankyo Co., Ltd., Novartis Pharma K.K., and Takeda Pharmaceutical Co., Ltd.; has received scholarship grants from Astellas Pharma Inc., Daiichi Sankyo Co., Ltd., Kissei Pharmaceutical Co., Ltd., Kyowa Hakko Kirin Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., Sanofi K. K., Sumitomo Dainippon Pharma Co., Ltd., Taisho Toyama Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd.; and has belonged to courses endowed by Kowa Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd. Masakazu Haneda has received speaker honorarium/lecture fees from Astellas Pharma Inc., Kowa Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novartis Pharma K.K., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., Sanofi K.K., Taisho Pharmaceutical Co., Ltd., and Taisho Toyama Pharmaceutical Co., Ltd.; and has received scholarship grants from Astellas Pharma Inc., Daiichi Sankyo Co., Ltd., Eli Lilly Japan K.K., Johnson & Johnson K.K., Kissei Pharmaceutical Co., Ltd., Kowa Pharmaceutical Co., Ltd., Kyowa Hakko Kirin Co., Ltd., Mitsubishi Tanabe Pharma Corporation, MSD K.K., Nippon Boehringer Ingelheim Co., Ltd., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Sanofi K.K., Shionogi & Co., Ltd., Taisho Toyama Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd. Hiroshi Ito has received speaker honorarium/lecture fees from Daiichi Sankyo Co., Ltd. and Mitsubishi Tanabe Pharma Corporation, and has received scholarship grants from Daiichi Sankyo Co., Ltd. and Mitsubishi Tanabe Pharma Corporation. Kazuyo Sasaki is an employee of the Mitsubishi Tanabe Pharma Corporation. Makoto Ueno is an employee of the Mitsubishi Tanabe Pharma Corporation. Sonoe Hiraide is an employee of the Mitsubishi Tanabe Pharma Corporation. Miyuki Matsukawa is an employee of the Mitsubishi Tanabe Pharma Corporation. The protocol of RUBY surveillance was approved by the Ministry of Health, Labour and Welfare of the Japan Government. The post-marketing surveillance program is ongoing and is carried out by the Mitsubishi Tanabe Pharma Corporation, in accordance with the Japanese Ministry directive on Good Post-marketing Study Practice Guidelines; in compliance with Japanese regulations for post-marketing surveillance, it was not necessary to obtain informed consent from patients. All analyses in the present surveillance were performed on a fully anonymized dataset. The datasets analyzed during the current study are not publicly available due to protection of individual patient confidentiality, but are available from the corresponding author on reasonable request. 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/), 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. To view enhanced digital features for this article go to 10.6084/m9.figshare.6155075. Funding Information: Funding. The RUBY surveillance program was funded by Mitsubishi Tanabe Pharma Corporation, and Daiichi Sankyo Co. Ltd. Medical writing support was funded by the Mitsubishi Tanabe Pharma Corporation, Osaka, Japan. The article processing charges and open access fee for this publication were funded by Mitsubishi Tanabe Pharma Corp. All authors had full access to all of the data in this study and take complete responsibility for the integrity of the data and accuracy of the data analysis. Publisher Copyright: © 2018, The Author(s).
PY - 2018/6/1
Y1 - 2018/6/1
N2 - Introduction: Healthy eating is a critical aspect of the prevention and management of type 2 diabetes (T2DM). Disrupted eating patterns can result in poor glucose control and increase the likelihood of diabetic complications. Teneligliptin inhibits dipeptidyl peptidase-4 activity for 24 h and suppresses postprandial hyperglycemia after all three daily meals. This interim analysis of data from the large-scale post-marketing surveillance of teneligliptin (RUBY) in Japan examined eating patterns and their relationship with metabolic parameters and diabetic complications. We also examined whether eating patterns affected safety and efficacy of teneligliptin. Methods: We analyzed baseline data from survey forms collected in RUBY between May 2013 and June 2017, including patient characteristics, metabolic parameters, and eating patterns (eating three meals per day or not; timing of evening meal) before teneligliptin treatment was initiated. Safety and efficacy of 12 months’ teneligliptin (20–40 mg/day) treatment was assessed. Results: Data from 10,532 patients were available for analysis. Most patients who did not eat three meals per day (n =757) or who ate their evening meal after 10 PM (n =206) were 64 years old or younger. At baseline, glycated hemoglobin (HbA1c), fasting blood glucose, triglycerides, total and low-density lipoprotein cholesterol, body mass index, alanine aminotransferase, and aspartate aminotransferase levels were higher in those patients who did not eat three meals per day (p < 0.05) or who ate their evening meal late (p < 0.05). Diabetic complications were more common in patients who did not eat three meals per day. Treatment with teneligliptin reduced HbA1c over 6 or 12 months across all eating patterns, with a low incidence of adverse drug reactions. Conclusions: Eating patterns may be associated with altered metabolic parameters and diabetic complications among Japanese patients with T2DM. Teneligliptin may be well tolerated and improve hyperglycemia in patients with T2DM irrespective of eating patterns. Funding: Mitsubishi Tanabe Pharma Corporation and Daiichi Sankyo Co. Ltd. Trial Registration Number: Japic CTI-153047.
AB - Introduction: Healthy eating is a critical aspect of the prevention and management of type 2 diabetes (T2DM). Disrupted eating patterns can result in poor glucose control and increase the likelihood of diabetic complications. Teneligliptin inhibits dipeptidyl peptidase-4 activity for 24 h and suppresses postprandial hyperglycemia after all three daily meals. This interim analysis of data from the large-scale post-marketing surveillance of teneligliptin (RUBY) in Japan examined eating patterns and their relationship with metabolic parameters and diabetic complications. We also examined whether eating patterns affected safety and efficacy of teneligliptin. Methods: We analyzed baseline data from survey forms collected in RUBY between May 2013 and June 2017, including patient characteristics, metabolic parameters, and eating patterns (eating three meals per day or not; timing of evening meal) before teneligliptin treatment was initiated. Safety and efficacy of 12 months’ teneligliptin (20–40 mg/day) treatment was assessed. Results: Data from 10,532 patients were available for analysis. Most patients who did not eat three meals per day (n =757) or who ate their evening meal after 10 PM (n =206) were 64 years old or younger. At baseline, glycated hemoglobin (HbA1c), fasting blood glucose, triglycerides, total and low-density lipoprotein cholesterol, body mass index, alanine aminotransferase, and aspartate aminotransferase levels were higher in those patients who did not eat three meals per day (p < 0.05) or who ate their evening meal late (p < 0.05). Diabetic complications were more common in patients who did not eat three meals per day. Treatment with teneligliptin reduced HbA1c over 6 or 12 months across all eating patterns, with a low incidence of adverse drug reactions. Conclusions: Eating patterns may be associated with altered metabolic parameters and diabetic complications among Japanese patients with T2DM. Teneligliptin may be well tolerated and improve hyperglycemia in patients with T2DM irrespective of eating patterns. Funding: Mitsubishi Tanabe Pharma Corporation and Daiichi Sankyo Co. Ltd. Trial Registration Number: Japic CTI-153047.
KW - Dipeptidyl peptidase-4 inhibitor
KW - Eating pattern
KW - HbA1c
KW - Post-marketing surveillance
KW - Teneligliptin
KW - Type 2 diabetes
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UR - http://www.scopus.com/inward/citedby.url?scp=85047161492&partnerID=8YFLogxK
U2 - 10.1007/s12325-018-0704-2
DO - 10.1007/s12325-018-0704-2
M3 - Article
C2 - 29777520
AN - SCOPUS:85047161492
SN - 0741-238X
VL - 35
SP - 817
EP - 831
JO - Advances in Therapy
JF - Advances in Therapy
IS - 6
ER -