TY - JOUR
T1 - Tofogliflozin long-term effects on atherosclerosis progression and major clinical parameters in patients with type 2 diabetes mellitus lacking a history of cardiovascular disease
T2 - a 2-year extension study of the UTOPIA trial
AU - the UTOPIA study investigators
AU - Katakami, Naoto
AU - Mita, Tomoya
AU - Yoshii, Hidenori
AU - Shiraiwa, Toshihiko
AU - Yasuda, Tetsuyuki
AU - Okada, Yosuke
AU - Kurozumi, Akira
AU - Hatazaki, Masahiro
AU - Kaneto, Hideaki
AU - Osonoi, Takeshi
AU - Yamamoto, Tsunehiko
AU - Kuribayashi, Nobuichi
AU - Maeda, Kazuhisa
AU - Yokoyama, Hiroki
AU - Kosugi, Keisuke
AU - Ohtoshi, Kentaro
AU - Hayashi, Isao
AU - Sumitani, Satoru
AU - Tsugawa, Mamiko
AU - Ryomoto, Kayoko
AU - Kato, Ken
AU - Nakamura, Tadashi
AU - Kawashima, Satoshi
AU - Sato, Yasunori
AU - Watada, Hirotaka
AU - Shimomura, Iichiro
AU - Komiyama, K.
AU - Shimizu, T.
AU - Kamei, S.
AU - Kinoshita, T.
AU - Shimoda, M.
AU - Saito, M.
AU - Fujiki, N.
AU - Fujita, Y.
AU - Shimizu, S.
AU - Umayahara, Y.
AU - Irie, Y.
AU - Kataoka, R.
AU - Kiyohara, Y.
AU - Ohashi, M.
AU - Ryomoto, K.
AU - Takahi, Y.
AU - Fujishima, Y.
AU - Fujita, Y.
AU - Fukuhara, A.
AU - Fukui, K.
AU - Hosokawa, Y.
AU - Imagawa, A.
AU - Iwahashi, H.
AU - Matsushita, K.
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Background: This study aimed to assess the long-term effects of tofogliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, on atherosclerosis progression and major clinical parameters in patients with type 2 diabetes lacking an apparent history of cardiovascular disease. Methods: This was a prospective observational 2-year extension study of the “Using TOfogliflozin for Possible better Intervention against Atherosclerosis for type 2 diabetes patients (UTOPIA)” trial, a 2-year randomized intervention study. The primary endpoints represented changes in the carotid intima-media thickness (IMT). Secondary endpoints included brachial-ankle pulse wave velocity (baPWV) and biomarkers for glucose metabolism, lipid metabolism, renal function, and cardiovascular risks. Results: The mean IMT of the common carotid artery (IMT-CCA) significantly decreased in both the tofogliflozin (− 0.067 mm, standard error 0.009, p < 0.001) and conventional treatment groups (− 0.080 mm, SE 0.009, p < 0.001) throughout the follow-up period; however, no significant intergroup differences in the changes (0.013 mm, 95% confidence interval (CI) − 0.012 to 0.037, p = 0.32) were observed in a mixed-effects model for repeated measures. baPWV significantly increased in the conventional treatment group (82.7 ± 210.3 cm/s, p = 0.008) but not in the tofogliflozin group (− 17.5 ± 221.3 cm/s, p = 0.54), resulting in a significant intergroup difference in changes (− 100.2 cm/s, 95% CI − 182.8 to − 17.5, p = 0.018). Compared to the conventional treatment group, tofogliflozin significantly improved the hemoglobin A1c and high-density lipoprotein cholesterol levels, body mass index, abdominal circumference, and systolic blood pressure. The frequencies of total and serious adverse events did not vary significantly between the groups. Conclusions: Tofogliflozin was not associated with improved inhibition of carotid wall thickening but exerted long-term positive effects on various cardiovascular risk factors and baPWV while showing a good safety profile.
AB - Background: This study aimed to assess the long-term effects of tofogliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, on atherosclerosis progression and major clinical parameters in patients with type 2 diabetes lacking an apparent history of cardiovascular disease. Methods: This was a prospective observational 2-year extension study of the “Using TOfogliflozin for Possible better Intervention against Atherosclerosis for type 2 diabetes patients (UTOPIA)” trial, a 2-year randomized intervention study. The primary endpoints represented changes in the carotid intima-media thickness (IMT). Secondary endpoints included brachial-ankle pulse wave velocity (baPWV) and biomarkers for glucose metabolism, lipid metabolism, renal function, and cardiovascular risks. Results: The mean IMT of the common carotid artery (IMT-CCA) significantly decreased in both the tofogliflozin (− 0.067 mm, standard error 0.009, p < 0.001) and conventional treatment groups (− 0.080 mm, SE 0.009, p < 0.001) throughout the follow-up period; however, no significant intergroup differences in the changes (0.013 mm, 95% confidence interval (CI) − 0.012 to 0.037, p = 0.32) were observed in a mixed-effects model for repeated measures. baPWV significantly increased in the conventional treatment group (82.7 ± 210.3 cm/s, p = 0.008) but not in the tofogliflozin group (− 17.5 ± 221.3 cm/s, p = 0.54), resulting in a significant intergroup difference in changes (− 100.2 cm/s, 95% CI − 182.8 to − 17.5, p = 0.018). Compared to the conventional treatment group, tofogliflozin significantly improved the hemoglobin A1c and high-density lipoprotein cholesterol levels, body mass index, abdominal circumference, and systolic blood pressure. The frequencies of total and serious adverse events did not vary significantly between the groups. Conclusions: Tofogliflozin was not associated with improved inhibition of carotid wall thickening but exerted long-term positive effects on various cardiovascular risk factors and baPWV while showing a good safety profile.
KW - Atherosclerosis
KW - Brachial-ankle pulse wave velocity
KW - Cardiovascular risk factors
KW - Carotid intima-media thickness
KW - Sodium-glucose cotransporter 2 inhibitor
KW - Tofogliflozin
UR - https://www.scopus.com/pages/publications/85162791632
UR - https://www.scopus.com/pages/publications/85162791632#tab=citedBy
U2 - 10.1186/s12933-023-01879-4
DO - 10.1186/s12933-023-01879-4
M3 - Article
C2 - 37349722
AN - SCOPUS:85162791632
SN - 1475-2840
VL - 22
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 143
ER -