TY - JOUR
T1 - Effect of sitagliptin on the echocardiographic parameters of left ventricular diastolic function in patients with type 2 diabetes
T2 - A subgroup analysis of the PROLOGUE study
AU - for the PROLOGUE Study Investigators
AU - Yamada, Hirotsugu
AU - Tanaka, Atsushi
AU - Kusunose, Kenya
AU - Amano, Rie
AU - Matsuhisa, Munehide
AU - Daida, Hiroyuki
AU - Ito, Masaaki
AU - Tsutsui, Hiroyuki
AU - Nanasato, Mamoru
AU - Kamiya, Haruo
AU - Bando, Yasuko K.
AU - Odawara, Masato
AU - Yoshida, Hisako
AU - Murohara, Toyoaki
AU - Sata, Masataka
AU - Node, Koichi
N1 - Funding Information:
HYa received honoraria from MSD, research grant from MSD and Ono. AT, KK, and RA declares no competing interests. MM received honoraria from Astellas, Eli Lilly, Mitsubishi Tanabe, Novo Nordisk, Sanofi, and Takeda, research grant from Astellas, Nihon Unisys, Nikkiso, and Terumo. HD received honoraria from Astellas, AstraZeneca, Bayer, Boehringer Ingelheim, Daiichi Sankyo, GlaxoS-mithKline, Kowa, Medtronic Japan, Mitsubishi Tanabe, Mochida, MSD, Ono, Pfizer, Sanofi, Shionogi, Takeda and Terumo, research funding from Abbott Vascular Japan, Astellas, Bayer, Boehringer Ingelheim, Boston Scientific Japan, Bristol-Myers, Daiichi Sankyo, Kaken, Kowa, MSD, Novartis, Otsuka, Pfizer, Philips Respironics GK, Sanofi, Sanwa Kagaku Kenkyusho, Shionogi, Sumitomo Dainip-pon and Takeda. MI received honoraria from Daiichi Sankyo and Pfizer, research funding from Astellas, Biotronik, Bristol-Myers, Daiichi Sankyo, GlaxoSmithKline, Mitsubishi Tanabe, MSD, Novartis, Otsuka, Pfizer, Shionogi, Sumitomo Dainip-pon and Takeda. HT received honoraria from Bristol-Myers, Daiichi Sankyo, Mit-subishi Tanabe and Ono, research funding from Astellas, Boehringer Ingelheim, Boston Scientific Japan, Daiichi Sankyo, Mitsubishi Tanabe, Otsuka, Takeda and Teijin Pharma. MN declares no competing interests. HK declares no competing interests. YKB received honoraria from AstraZeneca, Mitsubishi Tanabe, MSD, and Takeda, research grant from AstraZeneca, Daiichi Sankyo, Mitsubishi Tanabe, MSD, and Takeda. MO received honoraria from Astellas, Boehringer Ingelheim, Daiichi Sankyo, Eli Lilly, Kowa, Merck, Mitsubishi Tanabe, Novartis, Ono and Sanofi. HYo declares no competing interests. TM received honoraria from Bayer, Boehringer Ingelheim, Daiichi Sankyo, Kowa, Mitsubishi Tanabe, MSD, Pfizer, Sumitomo Dainippon, and Takeda, research grant from Astellas, Boehringer Ingelheim, Daiichi Sankyo, Kowa, Mitsubishi Tanabe, MSD, Novartis, Otsuka, Pfizer, Sanofi, Sumitomo Dainippon, Takeda, and Teijin Pharma. KN received honoraria from Astellas, Boehringer Ingelheim, Daiichi Sankyo, Merck, Mitsubishi Tanabe, Sanofi, and Takeda. MS received honoraria from MSD, research grant from MSD and Ono. KN received research funding from Astellas, Boehringer Ingelheim, Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology in Japan, Mitsubishi Tanabe, Sanwa Kagaku Kenkyusho, Takeda, and Teijin Pharma.
Funding Information:
This study is supported by a research grant from the Clinical Research Promotion Foundation (No. 1026). The funding body had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/5/11
Y1 - 2017/5/11
N2 - Background: Diabetes is associated closely with an increased risk of cardiovascular events, including diastolic dysfunction and heart failure that leads to a shortening of life expectancy. It is therefore extremely valuable to evaluate the impact of antidiabetic agents on cardiac function. However, the influence of dipeptidyl peptidase 4 inhibitors on cardiac function is controversial and a major matter of clinical concern. We therefore evaluated the effect of sitagliptin on echocardiographic parameters of diastolic function in patients with type 2 diabetes as a sub-analysis of the PROLOGUE study. Methods: Patients in the PROLOGUE study were assigned randomly to either add-on sitagliptin treatment or conventional antidiabetic treatment. Of the 463 patients in the overall study, 115 patients (55 in the sitagliptin group and 60 in the conventional group) who had complete echocardiographic data of the ratio of peak early diastolic transmitral flow velocity (E) to peak early diastolic mitral annular velocity (e') at baseline and after 12 and 24 months were included in this study. The primary endpoint of this post hoc sub-analysis was a comparison of the changes in the ratio of E to e' (E/e') between the two groups from baseline to 24 months. Results: The baseline-adjusted change in E/e' during 24 months was significantly lower in the sitagliptin group than in the conventional group (-0.18 ± 0.55 vs. 1.91 ± 0.53, p = 0.008), irrespective of a higher E/e' value at baseline in the sitagliptin group. In analysis of covariance, sitagliptin treatment was significantly associated with change in E/e' over 24 months (β = -9.959, p = 0.001), independent of other clinical variables at baseline such as blood pressure, HbA1c, and medications for diabetes. Changes in other clinical variables including blood pressure and glycemic parameters, and echocardiographic parameters, such as cardiac structure and systolic function, were comparable between the two groups. There was also no significant difference in the serum levels of N-terminal-pro brain natriuretic peptide and high-sensitive C-reactive protein between the two groups during the study period. Conclusions: Adding sitagliptin to conventional antidiabetic regimens in patients with T2DM for 24 months attenuated the annual exacerbation in the echocardiographic parameter of diastolic dysfunction (E/e') independent of other clinical variables such as blood pressure and glycemic control. Trial registration UMIN000004490 (University Hospital Medical Information Network Clinical Trials). https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005356
AB - Background: Diabetes is associated closely with an increased risk of cardiovascular events, including diastolic dysfunction and heart failure that leads to a shortening of life expectancy. It is therefore extremely valuable to evaluate the impact of antidiabetic agents on cardiac function. However, the influence of dipeptidyl peptidase 4 inhibitors on cardiac function is controversial and a major matter of clinical concern. We therefore evaluated the effect of sitagliptin on echocardiographic parameters of diastolic function in patients with type 2 diabetes as a sub-analysis of the PROLOGUE study. Methods: Patients in the PROLOGUE study were assigned randomly to either add-on sitagliptin treatment or conventional antidiabetic treatment. Of the 463 patients in the overall study, 115 patients (55 in the sitagliptin group and 60 in the conventional group) who had complete echocardiographic data of the ratio of peak early diastolic transmitral flow velocity (E) to peak early diastolic mitral annular velocity (e') at baseline and after 12 and 24 months were included in this study. The primary endpoint of this post hoc sub-analysis was a comparison of the changes in the ratio of E to e' (E/e') between the two groups from baseline to 24 months. Results: The baseline-adjusted change in E/e' during 24 months was significantly lower in the sitagliptin group than in the conventional group (-0.18 ± 0.55 vs. 1.91 ± 0.53, p = 0.008), irrespective of a higher E/e' value at baseline in the sitagliptin group. In analysis of covariance, sitagliptin treatment was significantly associated with change in E/e' over 24 months (β = -9.959, p = 0.001), independent of other clinical variables at baseline such as blood pressure, HbA1c, and medications for diabetes. Changes in other clinical variables including blood pressure and glycemic parameters, and echocardiographic parameters, such as cardiac structure and systolic function, were comparable between the two groups. There was also no significant difference in the serum levels of N-terminal-pro brain natriuretic peptide and high-sensitive C-reactive protein between the two groups during the study period. Conclusions: Adding sitagliptin to conventional antidiabetic regimens in patients with T2DM for 24 months attenuated the annual exacerbation in the echocardiographic parameter of diastolic dysfunction (E/e') independent of other clinical variables such as blood pressure and glycemic control. Trial registration UMIN000004490 (University Hospital Medical Information Network Clinical Trials). https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005356
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U2 - 10.1186/s12933-017-0546-2
DO - 10.1186/s12933-017-0546-2
M3 - Article
C2 - 28490337
AN - SCOPUS:85019079497
SN - 1475-2840
VL - 16
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 63
ER -