Takayama Tadateru, Komatsu Sei, Ueda Yasunori, Fukushima Seiji, Hiro Takafumi, Hirayama Atsushi, Saito Satoshi
Division of Cardiology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Department of Cardiology, Osaka Gyoumeikan Hospital, Osaka, Japan.
Am J Cardiol. 2016 Apr 15;117(8):1206-12. doi: 10.1016/j.amjcard.2016.01.013. Epub 2016 Jan 28.
Diminishing yellow color, evaluated by coronary angioscopy, is associated with plaque stabilization and regression. Our aim was to assess the effect of aggressive lipid-lowering therapy with rosuvastatin on plaque regression and instability. Thirty-seven patients with stable angina or silent myocardial ischemia who planned to undergo elective percutaneous coronary intervention and had angioscopic yellow plaques of grade 2 or more were randomized to high-dose (group H, 20 mg/day, n = 18) or low-dose (group L, 2.5 mg/day, n = 19) rosuvastatin therapy for 48 weeks. Yellow plaque was graded on a 4-point scale of 0 (white) to 3 (bright yellow) by angioscopy, and plaque volume was determined by intravascular ultrasound for plaques with a length of 5 to 15 mm. Color and volume were assessed at baseline and after 48 weeks by the investigators blinded to the rosuvastatin dosage, and were compared between the 2 dosing groups. The level of low-density lipoprotein-cholesterol decreased from 130.3 ± 25.5 mg/dl to 61.7 ± 16.5 mg/dl (-50 ± 19%: high intensity) in group H (p <0.001) and from 130.9 ± 28.5 mg/dl to 89.7 ± 29.0 mg/dl (-30 ± 22%: moderate intensity) in group L (mean ± SD, p <0.001). The average color grade of yellow plaques decreased from 2.0 to 1.5 in group H (p <0.001) and from 2.0 to 1.6 in group L (p <0.001) after 48 weeks. Plaque volume decreased significantly in group H but not in group L. The percent change in plaque volume was significantly larger in group H than in group L (p = 0.005). In conclusion, both high-dose and low-dose rosuvastatin increased plaque stability. However, high-dose rosuvastatin was more effective than low-dose rosuvastatin in inducing plaque volume regression. Clinical Trial Registration No: UMIN-CTR, UMIN000003276.
通过冠状动脉血管镜评估,黄色减退与斑块稳定及消退相关。我们的目的是评估瑞舒伐他汀强化降脂治疗对斑块消退及不稳定性的影响。37例计划接受择期经皮冠状动脉介入治疗且血管镜检查显示黄色斑块分级为2级或更高的稳定型心绞痛或无症状心肌缺血患者,被随机分为高剂量组(H组,20毫克/天,n = 18)或低剂量组(L组,2.5毫克/天,n = 19),接受瑞舒伐他汀治疗48周。血管镜检查将黄色斑块按0(白色)至3(亮黄色)的4分制分级,对于长度为5至15毫米的斑块,通过血管内超声测定斑块体积。由对瑞舒伐他汀剂量不知情的研究人员在基线和48周后评估颜色和体积,并在两个给药组之间进行比较。H组低密度脂蛋白胆固醇水平从130.3±25.5毫克/分升降至61.7±16.5毫克/分升(-50±19%:高强度)(p<0.001),L组从130.9±28.5毫克/分升降至89.7±29.0毫克/分升(-30±22%:中等强度)(均数±标准差,p<0.001)。48周后,H组黄色斑块的平均颜色分级从2.0降至1.5(p<0.001),L组从2.0降至1.6(p<0.001)。H组斑块体积显著减小,而L组未减小。H组斑块体积的变化百分比显著大于L组(p = 0.005)。总之,高剂量和低剂量瑞舒伐他汀均增加了斑块稳定性。然而,高剂量瑞舒伐他汀在诱导斑块体积消退方面比低剂量瑞舒伐他汀更有效。临床试验注册号:UMIN-CTR,UMIN000003276。