Tanaka Atsushi, Murohara Toyoaki, Taguchi Isao, Eguchi Kazuo, Suzuki Makoto, Kitakaze Masafumi, Sato Yasunori, Ishizu Tomoko, Higashi Yukihito, Yamada Hirotsugu, Nanasato Mamoru, Shimabukuro Michio, Teragawa Hiroki, Ueda Shinichiro, Kodera Satoshi, Matsuhisa Munehide, Kadokami Toshiaki, Kario Kazuomi, Nishio Yoshihiko, Inoue Teruo, Maemura Koji, Oyama Jun-Ichi, Ohishi Mitsuru, Sata Masataka, Tomiyama Hirofumi, Node Koichi
Department of Cardiovascular Medicine, Saga University, Saga, Japan.
Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Cardiovasc Diabetol. 2016 Sep 13;15(1):133. doi: 10.1186/s12933-016-0449-7.
Type 2 diabetes mellitus is associated strongly with an increased risk of micro- and macro-vascular complications, leading to impaired quality of life and shortened life expectancy. In addition to appropriate glycemic control, multi-factorial intervention for a wide range of risk factors, such as hypertension and dyslipidemia, is crucial for management of diabetes. A recent cardiovascular outcome trial in diabetes patients with higher cardiovascular risk demonstrated that a SGLT2 inhibitor markedly reduced mortality, but not macro-vascular events. However, to date there is no clinical evidence regarding the therapeutic effects of SGLT2 inhibitors on arteriosclerosis. The ongoing PROTECT trial was designed to assess whether the SGLT2 inhibitors, ipragliflozin, prevented progression of carotid intima-media thickness in Japanese patients with type 2 diabetes mellitus.
A total of 480 participants with type 2 diabetes mellitus with a HbA1c between 6 and 10 % despite receiving diet/exercise therapy and/or standard anti-diabetic agents for at least 3 months, will be randomized systematically (1:1) into either ipragliflozin or control (continuation of conventional therapy) groups. After randomization, ipragliflozin (50-100 mg once daily) will be added on to the background therapy in participants assigned to the ipragliflozin group. The primary endpoint of the study is the change in mean intima-media thickness of the common carotid artery from baseline to 24 months. Images of carotid intima-media thickness will be analyzed at a central core laboratory in a blinded manner. The key secondary endpoints include the change from baseline in other parameters of carotid intima-media thickness, various metabolic parameters, and renal function. Other cardiovascular functional tests are also planned for several sub-studies.
The PROTECT study is the first to assess the preventive effect of ipragliflozin on progression of carotid atherosclerosis using carotid intima-media thickness as a surrogate marker. The study has potential to clarify the protective effects of ipragliflozin on atherosclerosis. Trial registration Unique Trial Number, JPRN/UMIN000018440 ( https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000021348 ).
2型糖尿病与微血管和大血管并发症风险增加密切相关,会导致生活质量受损和预期寿命缩短。除了适当的血糖控制外,针对高血压和血脂异常等多种危险因素的多因素干预对于糖尿病的管理至关重要。最近一项针对心血管风险较高的糖尿病患者的心血管结局试验表明,钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂可显著降低死亡率,但对大血管事件无影响。然而,迄今为止,尚无关于SGLT2抑制剂对动脉硬化治疗效果的临床证据。正在进行的PROTECT试验旨在评估SGLT2抑制剂依帕列净是否能预防日本2型糖尿病患者颈动脉内膜中层厚度的进展。
共有480名2型糖尿病患者,尽管接受饮食/运动疗法和/或标准抗糖尿病药物治疗至少3个月,但其糖化血红蛋白(HbA1c)仍在6%至10%之间,将被系统地随机分为依帕列净组或对照组(继续常规治疗),比例为1:1。随机分组后,依帕列净组的参与者将在背景治疗基础上加用依帕列净(每日一次,50 - 100毫克)。该研究的主要终点是从基线到24个月时颈总动脉平均内膜中层厚度的变化。颈动脉内膜中层厚度的图像将在中央核心实验室以盲法进行分析。关键的次要终点包括颈动脉内膜中层厚度的其他参数、各种代谢参数和肾功能从基线的变化。还计划对几个子研究进行其他心血管功能测试。
PROTECT研究是首个以颈动脉内膜中层厚度作为替代标志物评估依帕列净对颈动脉粥样硬化进展预防作用的研究。该研究有可能阐明依帕列净对动脉粥样硬化的保护作用。试验注册号:唯一试验编号,JPRN/UMIN000018440(https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000021348)。