TY - JOUR
T1 - Lack of impact of ipragliflozin on endothelial function in patients with type 2 diabetes
T2 - sub-analysis of the PROTECT study
AU - the PROTECT investigators
AU - Kishimoto, Shinji
AU - Higashi, Yukihito
AU - Imai, Takumi
AU - Eguchi, Kazuo
AU - Fukumoto, Kazuo
AU - Tomiyama, Hirofumi
AU - Maemura, Koji
AU - Tanaka, Atsushi
AU - Node, Koichi
AU - Murohara, Toyoaki
AU - Kitakaze, Masafumi
AU - Nishio, Yoshihiko
AU - Inoue, Teruo
AU - Ohishi, Mitsuru
AU - Kario, Kazuomi
AU - Sata, Masataka
AU - Shimabukuro, Michio
AU - Shimizu, Wataru
AU - Jinnouchi, Hideaki
AU - Taguchi, Isao
AU - Suzuki, Makoto
AU - Ando, Shinichi
AU - Kamiya, Haruo
AU - Sakamoto, Tomohiro
AU - Teragawa, Hiroki
AU - Nanasato, Mamoru
AU - Matsuhisa, Munehide
AU - Ako, Junya
AU - Aso, Yoshimasa
AU - Ishihara, Masaharu
AU - Kitagawa, Kazuo
AU - Yamashina, Akira
AU - Ishizu, Tomoko
AU - Ikehara, Yumi
AU - Ueda, Shinichiro
AU - Takamori, Ayako
AU - Yoshida, Hisako
AU - Mori, Miki
AU - Yamaguchi, Kaori
AU - Asaka, Machiko
AU - Kaneko, Tetsuya
AU - Sakuma, Masashi
AU - Toyoda, Shigeru
AU - Nasuno, Takahisa
AU - Kageyama, Michiya
AU - Teruo, Jojima
AU - Toshie, Iijima
AU - Kishi, Haruka
AU - Yamada, Hirotsugu
AU - Okumura, Takahiro
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Background: We assessed the impact of 24 months of treatment with ipragliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, on endothelial function in patients with type 2 diabetes as a sub-analysis of the PROTECT study. Methods: In the PROTECT study, patients were randomized to receive either standard antihyperglycemic treatment (control group, n = 241) or add-on ipragliflozin treatment (ipragliflozin group, n = 241) in a 1:1 ratio. Among the 482 patients in the PROTECT study, flow-mediated vasodilation (FMD) was assessed in 32 patients in the control group and 26 patients in the ipragliflozin group before and after 24 months of treatment. Results: HbA1c levels significantly decreased after 24 months of treatment compared to the baseline value in the ipragliflozin group, but not in the control group. However, there was no significant difference between the changes in HbA1c levels in the two groups (7.4 ± 0.8% vs. 7.0 ± 0.9% in the ipragliflozin group and 7.4 ± 0.7% vs. 7.3 ± 0.7% in the control group; P = 0.08). There was no significant difference between FMD values at baseline and after 24 months in both groups (5.2 ± 2.6% vs. 5.2 ± 2.6%, P = 0.98 in the ipragliflozin group; 5.4 ± 2.9% vs. 5.0 ± 3.2%, P = 0.34 in the control group). There was no significant difference in the estimated percentage change in FMD between the two groups (P = 0.77). Conclusions: Over a 24-month period, the addition of ipragliflozin to standard therapy in patients with type 2 diabetes did not change endothelial function assessed by FMD in the brachial artery. Trial registration : Registration Number for Clinical Trial: jRCT1071220089 (https://jrct.niph.go.jp/en-latest-detail/jRCT1071220089).
AB - Background: We assessed the impact of 24 months of treatment with ipragliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, on endothelial function in patients with type 2 diabetes as a sub-analysis of the PROTECT study. Methods: In the PROTECT study, patients were randomized to receive either standard antihyperglycemic treatment (control group, n = 241) or add-on ipragliflozin treatment (ipragliflozin group, n = 241) in a 1:1 ratio. Among the 482 patients in the PROTECT study, flow-mediated vasodilation (FMD) was assessed in 32 patients in the control group and 26 patients in the ipragliflozin group before and after 24 months of treatment. Results: HbA1c levels significantly decreased after 24 months of treatment compared to the baseline value in the ipragliflozin group, but not in the control group. However, there was no significant difference between the changes in HbA1c levels in the two groups (7.4 ± 0.8% vs. 7.0 ± 0.9% in the ipragliflozin group and 7.4 ± 0.7% vs. 7.3 ± 0.7% in the control group; P = 0.08). There was no significant difference between FMD values at baseline and after 24 months in both groups (5.2 ± 2.6% vs. 5.2 ± 2.6%, P = 0.98 in the ipragliflozin group; 5.4 ± 2.9% vs. 5.0 ± 3.2%, P = 0.34 in the control group). There was no significant difference in the estimated percentage change in FMD between the two groups (P = 0.77). Conclusions: Over a 24-month period, the addition of ipragliflozin to standard therapy in patients with type 2 diabetes did not change endothelial function assessed by FMD in the brachial artery. Trial registration : Registration Number for Clinical Trial: jRCT1071220089 (https://jrct.niph.go.jp/en-latest-detail/jRCT1071220089).
KW - Endothelial function
KW - Ipragliflozin
KW - Sodium-glucose cotransporter-2 inhibitors
KW - Type 2 diabetes
UR - https://www.scopus.com/pages/publications/85159706342
UR - https://www.scopus.com/pages/publications/85159706342#tab=citedBy
U2 - 10.1186/s12933-023-01856-x
DO - 10.1186/s12933-023-01856-x
M3 - Article
C2 - 37210524
AN - SCOPUS:85159706342
SN - 1475-2840
VL - 22
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 119
ER -