Hagiwara Nobuhisa, Kawada-Watanabe Erisa, Koyanagi Ryo, Arashi Hiroyuki, Yamaguchi Junichi, Nakao Koichi, Tobaru Tetsuya, Tanaka Hiroyuki, Oka Toshiaki, Endoh Yasuhiro, Saito Katsumi, Uchida Tatsuro, Matsui Kunihiko, Ogawa Hiroshi
Department of Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University, 8-1, Kawada-cho, Shinjuku, Tokyo, 162-8666, Japan.
Division of Cardiology, Cardiovascular Center, Saisei-Kai Kumamoto Hospital, 5-3-1 Chikami, Minami-ku, Kumamoto-shi, Kumamoto 861-4193, Japan.
Eur Heart J. 2017 Aug 1;38(29):2264-2276. doi: 10.1093/eurheartj/ehx162.
To elucidate the effects of intensive LDL-C lowering treatment with a standard dose of statin and ezetimibe in patients with dyslipidaemia and high risk of coronary events, targeting LDL-C less than 70 mg/dL (1.8 mmol/L), compared with standard LDL-C lowering lipid monotherapy targeting less than 100 mg/dL (2.6 mmol/L).
The HIJ-PROPER study is a prospective, randomized, open-label trial to assess whether intensive LDL-C lowering with standard-dose pitavastatin plus ezetimibe reduces cardiovascular events more than standard LDL-C lowering with pitavastatin monotherapy in patients with acute coronary syndrome (ACS) and dyslipidaemia. Patients were randomized to intensive lowering (target LDL-C < 70 mg/dL [1.8 mmol/L]; pitavastatin plus ezetimibe) or standard lowering (target LDL-C 90 mg/dL to 100 mg/dL [2.3-2.6 mmol/L]; pitavastatin monotherapy). The primary endpoint was a composite of all-cause death, non-fatal myocardial infarction, non-fatal stroke, unstable angina, and ischaemia-driven revascularization. Between January 2010 and April 2013, 1734 patients were enroled at 19 hospitals in Japan. Patients were followed for at least 36 months. Median follow-up was 3.86 years. Mean follow-up LDL-C was 65.1 mg/dL (1.68 mmol/L) for pitavastatin plus ezetimibe and 84.6 mg/dL (2.19 mmol/L) for pitavastatin monotherapy. LDL-C lowering with statin plus ezetimibe did not reduce primary endpoint occurrence in comparison with standard statin monotherapy (283/864, 32.8% vs. 316/857, 36.9%; HR 0.89, 95% CI 0.76-1.04, P = 0.152). In, ACS patients with higher cholesterol absorption, represented by elevated pre-treatment sitosterol, was associated with significantly lower incidence of the primary endpoint in the statin plus ezetimibe group (HR 0.71, 95% CI 0.56-0.91).
Although intensive lowering with standard pitavastatin plus ezetimibe showed no more cardiovascular benefit than standard pitavastatin monotherapy in ACS patients with dyslipidaemia, statin plus ezetimibe may be more effective than statin monotherapy in patients with higher cholesterol absorption; further confirmation is needed.
UMIN000002742, registered as an International Standard Randomized Controlled Trial.
阐明采用标准剂量他汀类药物和依折麦布强化降低低密度脂蛋白胆固醇(LDL-C)治疗血脂异常且有高冠状动脉事件风险患者的效果,目标是使LDL-C低于70mg/dL(1.8mmol/L),并与目标为低于100mg/dL(2.6mmol/L)的标准降低LDL-C的降脂单药治疗进行比较。
HIJ-PROPER研究是一项前瞻性、随机、开放标签试验,旨在评估对于急性冠状动脉综合征(ACS)和血脂异常患者,标准剂量匹伐他汀加依折麦布强化降低LDL-C是否比匹伐他汀单药标准降低LDL-C能更多地减少心血管事件。患者被随机分为强化降低组(目标LDL-C<70mg/dL[1.8mmol/L];匹伐他汀加依折麦布)或标准降低组(目标LDL-C为90mg/dL至100mg/dL[2.3 - 2.6mmol/L];匹伐他汀单药治疗)。主要终点是全因死亡、非致命性心肌梗死、非致命性中风、不稳定型心绞痛和缺血驱动的血运重建的复合终点。在2010年1月至2013年4月期间,日本19家医院招募了1734例患者。对患者进行至少36个月的随访。中位随访时间为3.86年。匹伐他汀加依折麦布组的平均随访LDL-C为65.1mg/dL(1.68mmol/L),匹伐他汀单药治疗组为84.6mg/dL(2.19mmol/L)。与标准他汀类单药治疗相比,他汀类药物加依折麦布降低LDL-C并未降低主要终点事件的发生率(283/864,32.8%对316/857,36.9%;风险比0.89,95%置信区间0.76 - 1.04,P = 0.152)。在ACS患者中,以治疗前谷甾醇升高为代表的胆固醇吸收较高者,在他汀类药物加依折麦布组中主要终点事件的发生率显著较低(风险比0.71,95%置信区间0.56 - 0.91)。
尽管对于血脂异常的ACS患者,标准匹伐他汀加依折麦布强化降低治疗在心血管获益方面并不比标准匹伐他汀单药治疗更多,但他汀类药物加依折麦布在胆固醇吸收较高的患者中可能比他汀类单药治疗更有效;需要进一步证实。
UMIN000002742,注册为国际标准随机对照试验。