Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea; Yonsei-Cedars-Sinai Integrative Cardiovascular Imaging Research Center, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea.
Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea; Yonsei-Cedars-Sinai Integrative Cardiovascular Imaging Research Center, Yonsei University College of Medicine, Yonsei University Health System, Seoul, South Korea.
JACC Cardiovasc Imaging. 2018 Oct;11(10):1475-1484. doi: 10.1016/j.jcmg.2018.04.015. Epub 2018 Jun 13.
This study sought to describe the impact of statins on individual coronary atherosclerotic plaques.
Although statins reduce the risk of major adverse cardiovascular events, their long-term effects on coronary atherosclerosis remain unclear.
We performed a prospective, multinational study consisting of a registry of consecutive patients without history of coronary artery disease who underwent serial coronary computed tomography angiography at an interscan interval of ≥2 years. Atherosclerotic plaques were quantitatively analyzed for percent diameter stenosis (%DS), percent atheroma volume (PAV), plaque composition, and presence of high-risk plaque (HRP), defined by the presence of ≥2 features of low-attenuation plaque, positive arterial remodeling, or spotty calcifications.
Among 1,255 patients (60 ± 9 years of age; 57% men), 1,079 coronary artery lesions were evaluated in statin-naive patients (n = 474), and 2,496 coronary artery lesions were evaluated in statin-taking patients (n = 781). Compared with lesions in statin-naive patients, those in statin-taking patients displayed a slower rate of overall PAV progression (1.76 ± 2.40% per year vs. 2.04 ± 2.37% per year, respectively; p = 0.002) but more rapid progression of calcified PAV (1.27 ± 1.54% per year vs. 0.98 ± 1.27% per year, respectively; p < 0.001). Progression of noncalcified PAV and annual incidence of new HRP features were lower in lesions in statin-taking patients (0.49 ± 2.39% per year vs. 1.06 ± 2.42% per year and 0.9% per year vs. 1.6% per year, respectively; all p < 0.001). The rates of progression to >50% DS were not different (1.0% vs. 1.4%, respectively; p > 0.05). Statins were associated with a 21% reduction in annualized total PAV progression above the median and 35% reduction in HRP development.
Statins were associated with slower progression of overall coronary atherosclerosis volume, with increased plaque calcification and reduction of high-risk plaque features. Statins did not affect the progression of percentage of stenosis severity of coronary artery lesions but induced phenotypic plaque transformation. (Progression of AtheRosclerotic PlAque DetermIned by Computed TomoGraphic Angiography Imaging [PARADIGM]; NCT02803411).
本研究旨在描述他汀类药物对个体冠状动脉粥样硬化斑块的影响。
尽管他汀类药物降低了主要不良心血管事件的风险,但它们对冠状动脉粥样硬化的长期影响仍不清楚。
我们进行了一项前瞻性、多国研究,该研究包括一个连续患者登记处,这些患者没有冠心病史,并且在两次扫描间隔时间≥2 年内进行了连续冠状动脉计算机断层扫描血管造影术。对动脉粥样硬化斑块进行定量分析,以评估其直径狭窄百分比(%DS)、粥样斑块体积百分比(PAV)、斑块成分以及高危斑块(HRP)的存在情况,HRP 通过存在至少 2 个低衰减斑块、阳性动脉重构或点状钙化等特征来定义。
在 1255 例患者(60±9 岁;57%为男性)中,在他汀类药物初治患者(n=474)中评估了 1079 个冠状动脉病变,在他汀类药物治疗患者(n=781)中评估了 2496 个冠状动脉病变。与他汀类药物初治患者的病变相比,他汀类药物治疗患者的总体 PAV 进展速度较慢(每年分别为 1.76%±2.40%和 2.04%±2.37%;p=0.002),但钙化 PAV 的进展速度更快(每年分别为 1.27%±1.54%和 0.98%±1.27%;p<0.001)。他汀类药物治疗患者的非钙化 PAV 进展率和新 HRP 特征的年发生率较低(每年分别为 0.49%±2.39%和 1.06%±2.42%和 0.9%/年和 1.6%/年;均 p<0.001)。进展至>50%DS 的速率无差异(分别为 1.0%和 1.4%;p>0.05)。他汀类药物与每年 PAV 进展中位数以上的总 PAV 进展率降低 21%和 HRP 发展减少 35%相关。
他汀类药物与冠状动脉粥样硬化总体体积的进展较慢相关,与斑块钙化增加和高危斑块特征减少相关。他汀类药物不会影响冠状动脉病变狭窄严重程度百分比的进展,但会诱导表型斑块转化。(通过计算机断层扫描血管造影成像确定动脉粥样硬化斑块的进展[PARADIGM];NCT02803411)。