Hou Jingbo, Xing Lei, Jia Haibo, Vergallo Rocco, Soeda Tsunerari, Minami Yoshiyasu, Hu Sining, Yang Shuang, Zhang Shaosong, Lee Hang, Yu Bo, Jang Ik-Kyung
Department of Cardiology, The Second Affiliated Hospital of Harbin Medical University, The Key Laboratory of Myocardial Ischemia, Chinese Ministry of Education, Harbin, China.
Department of Cardiology, The Second Affiliated Hospital of Harbin Medical University, The Key Laboratory of Myocardial Ischemia, Chinese Ministry of Education, Harbin, China; Cardiology Division, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Am J Cardiol. 2016 Mar 1;117(5):800-6. doi: 10.1016/j.amjcard.2015.11.062. Epub 2015 Dec 13.
Despite marked clinical benefit, reduction in atheroma volume with statin therapy is minimal. Changes in plaque composition may explain this discrepancy. We aimed in the present study to assess the effect of statin therapy on coronary plaque composition and plaque volume using serial multimodality imaging. From an open-label, single-blinded study, patients with angiographically mild-to-moderate lesion were randomized to receive atorvastatin 60 (AT 60) mg or atorvastatin 20 (AT 20) mg for 12 months. Optical coherence tomography was used to assess fibrous cap thickness (FCT) and intravascular ultrasound to assess atheroma burden at 3 time points: baseline, at 6 months, and at 12 months. Thirty-six lipid-rich plaques in 27 patients with AT 60 mg and 30 lipid-rich plaques in 19 patients with AT 20 mg were enrolled in this study. Low-density lipoprotein cholesterol level was significantly decreased at 6 months without further reduction at 12 months. AT 60 mg induced greater reduction in low-density lipoprotein cholesterol compared with AT 20 mg. Optical coherence tomography revealed continuous increase in FCT from baseline to 6 months and to 12 months in both groups. AT 60 mg induced greater increase in FCT compared with AT 20 mg at both follow-up points. The prevalence of thin-cap fibroatheroma and the presence of macrophage at 6 months were significantly lower in AT 60 mg compared with AT 20 mg. Plaque burden did not change significantly in both groups. In conclusion, both intensive and moderate statin therapy stabilizes coronary plaques, with a greater benefit in the intensive statin group. However, no significant changes in plaque volume were observed over time regardless of the intensity of statin therapy.
尽管他汀类药物治疗具有显著的临床益处,但动脉粥样硬化斑块体积的减小却很微小。斑块成分的变化或许可以解释这一差异。在本研究中,我们旨在通过系列多模态成像评估他汀类药物治疗对冠状动脉斑块成分及斑块体积的影响。在一项开放标签、单盲研究中,将血管造影显示为轻度至中度病变的患者随机分为两组,分别接受60毫克阿托伐他汀(AT 60)或20毫克阿托伐他汀(AT 20)治疗,为期12个月。在3个时间点(基线、6个月和12个月),使用光学相干断层扫描评估纤维帽厚度(FCT),并使用血管内超声评估动脉粥样硬化负担。本研究纳入了27例接受AT 60毫克治疗患者的36个富含脂质的斑块,以及19例接受AT 20毫克治疗患者的30个富含脂质的斑块。低密度脂蛋白胆固醇水平在6个月时显著降低,在12个月时未进一步降低。与AT 20毫克相比,AT 60毫克导致低密度脂蛋白胆固醇的降低幅度更大。光学相干断层扫描显示,两组从基线到6个月再到12个月,FCT持续增加。在两个随访点,与AT 20毫克相比,AT 60毫克导致FCT增加幅度更大。与AT 20毫克相比,AT 60毫克组在6个月时薄帽纤维粥样瘤的患病率和巨噬细胞的存在情况显著更低。两组的斑块负担均未发生显著变化。总之,强化和中度他汀类药物治疗均可使冠状动脉斑块稳定,强化他汀类药物组获益更大。然而,无论他汀类药物治疗的强度如何,随时间推移均未观察到斑块体积有显著变化。