Rationale, Design, and Baseline Characteristics of the Utopia Trial for Preventing Diabetic Atherosclerosis Using an SGLT2 Inhibitor: A Prospective, Randomized, Open-Label, Parallel-Group Comparative Study

被引:13
|
作者
Katakami, Naoto [1 ,2 ]
Mita, Tomoya [3 ]
Yoshii, Hidenori [4 ]
Shiraiwa, Toshihiko [5 ]
Yasuda, Tetsuyuki [6 ]
Okada, Yosuke [7 ]
Umayahara, Yutaka [8 ]
Kaneto, Hideaki [9 ]
Osonoi, Takeshi [10 ]
Yamamoto, Tsunehiko [11 ]
Kuribayashi, Nobuichi [12 ]
Maeda, Kazuhisa [13 ]
Yokoyama, Hiroki [14 ]
Kosugi, Keisuke [15 ]
Ohtoshi, Kentaro [16 ]
Hayashi, Isao [17 ]
Sumitani, Satoru [18 ]
Tsugawa, Mamiko [19 ]
Ohashi, Makoto [20 ]
Taki, Hideki [21 ]
Nakamura, Tadashi [22 ]
Kawashima, Satoshi [23 ]
Sato, Yasunori [24 ]
Watada, Hirotaka [3 ]
Shimomura, Iichiro [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Metab Med, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Metab & Atherosclerosis, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[3] Juntendo Univ, Dept Endocrinol & Metab, Grad Sch Med, Bunkyo Ku, Hongo 2-1-1, Tokyo 1138421, Japan
[4] Juntendo Tokyo Koto Geriatr Med Ctr, Dept Med Diabetol & Endocrinol, Koto Ku, Tokyo 1360075, Japan
[5] Shiraiwa Med Clin, 4-10-24 Hozenji, Kashiwara, Osaka 5820005, Japan
[6] Osaka Police Hosp, Dept Endocrinol & Metab, Tennoji Ku, 10-13 Kitayama Cho, Osaka 5430035, Japan
[7] Univ Occupat & Environm Hlth, Sch Med, Dept Internal Med 1, Yahatanishi Ku, 1-1 Iseigaoka, Kitakyushu, Fukuoka 8078555, Japan
[8] Osaka Gen Med Ctr, Dept Endocrinol & Diabet, Sumiyoshi Ku, 3-1-56 Bandai Higashi, Osaka 5588558, Japan
[9] Kawasaki Med Sch, Dept Diabet Endocrinol & Metab, 577 Matsushima, Kurashiki, Okayama 7010192, Japan
[10] Nakakinen Clin, 745-5 Nakadai, Naka, Ibaraki 3110113, Japan
[11] Kansai Rosai Hosp, Diabet & Endocrinol, 3-1-69 Inabaso, Amagasaki, Hyogo, Japan
[12] Misaki Naika Clin, 6-44-9 Futawa Higashi, Funabashi, Chiba, Japan
[13] Kitasenri Maeda Clin, 4-119 Furuedai, Suita, Osaka 5650874, Japan
[14] Jiyugaoka Med Clin, West 6,South 6-4-3, Obihiro, Hokkaido 0800016, Japan
[15] Kosugi Med Clin, Tennoji Ku, 3-9 Tamatsukurimoto Cho, Osaka 5430014, Japan
[16] Otoshi Med Clin, Kita Ku, 8-47 Kakudacho, Osaka, Osaka 5300017, Japan
[17] Hayashi Clin, 3-9-23 Koshienguchi, Nishinomiya, Hyogo 6638113, Japan
[18] Nissay Hosp, Ctr Diabet & Endocrinol, Nishi Ku, 6-3-8 Itachibori, Osaka 5500012, Japan
[19] Ikeda Municipal Hosp, Dept Endocrinol & Metab, 3-1-18 Jonan, Ikeda, Osaka 5638510, Japan
[20] Osaka Rosai Hosp, Ctr Diabet Mellitus, Kita Ku, 1179-3 Nagasone Cho, Sakai, Osaka 5918025, Japan
[21] Natl Hosp Org, Osaka Natl Hosp, Diabet Ctr, Chuo Ku, 2-1-14 Hoenzaka, Osaka 5400006, Japan
[22] Kawasaki Hosp, Dept Internal Med, Hyogo Ku, 3-3-1 Higashiyamacho, Kobe, Hyogo 6520042, Japan
[23] Kanda Naika Clin, Abeno Ku, 5-21-3 Hannancho, Osaka, Osaka 5450021, Japan
[24] Chiba Univ, Grad Sch Med, Dept Global Clin Res, Chuo Ku, 1-8-1 Inohana, Chiba 2608677, Japan
关键词
Atherosclerosis; Diabetes; Intima-media thickness; SGLT2; inhibitor; Tofogliflozin; INTIMA-MEDIA THICKNESS; GLUCOSE COTRANSPORTER 2; CORONARY-HEART-DISEASE; CAROTID-ARTERY INTIMA; CARDIOVASCULAR EVENTS; GLYCEMIC CONTROL; ANTIDIABETIC AGENTS; JAPANESE PATIENTS; RISK-FACTORS; TYPE-2;
D O I
10.1007/s13300-017-0292-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Sodium-glucose co-transporter-2 (SGLT2) inhibitors are anti-diabetic agents that improve glycemic control with a low risk of hypoglycemia and ameliorate a variety of cardiovascular risk factors. The aim of the ongoing study described herein is to investigate the preventive effects of tofogliflozin, a potent and selective SGLT2 inhibitor, on the progression of atherosclerosis in subjects with type 2 diabetes (T2DM) using carotid intima-media thickness (IMT), an established marker of cardiovascular disease (CVD), as a marker. Methods: The Study of Using Tofogliflozin for Possible better Intervention against Atherosclerosis for type 2 diabetes patients (UTOPIA) trial is a prospective, randomized, open-label, blinded-endpoint, multicenter, and parallel-group comparative study. The aim was to recruit a total of 340 subjects with T2DM but no history of apparent CVD at 24 clinical sites and randomly allocate these to a tofogliflozin treatment group or a conventional treatment group using drugs other than SGLT2 inhibitors. As primary outcomes, changes in mean and maximum IMT of the common carotid artery during a 104-week treatment period will be measured by carotid echography. Secondary outcomes include changes in glycemic control, parameters related to beta-cell function and diabetic nephropathy, the occurrence of CVD and adverse events, and biochemical measurements reflecting vascular function. Conclusion: This is the first study to address the effects of SGLT2 inhibitors on the progression of carotid IMT in subjects with T2DM without a history of CVD. The results will be available in the very near future, and these findings are expected to provide clinical data that will be helpful in the prevention of diabetic atherosclerosis and subsequent CVD.
引用
收藏
页码:999 / 1013
页数:15
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