Department of Cardiovascular Medicine, Saga University.
Department of Clinical Epidemiology, Hyogo College of Medicine.
Circ J. 2022 Aug 25;86(9):1416-1427. doi: 10.1253/circj.CJ-22-0315. Epub 2022 Aug 5.
It is unknown whether beneficial effects of higher-dose statins on cardiovascular events are different according to the thrombotic risk in patients with chronic coronary syndrome (CCS).
The Randomized Evaluation of Aggressive or Moderate Lipid-Lowering Therapy with Pitavastatin in Coronary Artery Disease (REAL-CAD) study is a randomized trial comparing 4 mg and 1 mg pitavastatin in patients with CCS. This study categorized 12,413 patients into 3 strata according to the CREDO-Kyoto thrombotic risk score: low-risk (N=9,434; 4 mg: N=4,742, and 1 mg: N=4,692), intermediate-risk (N=2,415; 4 mg: N=1,188, and 1 mg: N=1,227); and high-risk (N=564; 4 mg: N=269, and 1 mg: N=295). The primary endpoint was a composite of cardiovascular death, non-fatal myocardial infarction, non-fatal ischemic stroke, or unstable angina. Cumulative 4-year incidence of the primary endpoint was significantly higher in the high-risk stratum than in the intermediate- and low-risk strata (11.0%, 6.3%, and 4.5%, P<0.0001). In the low-risk stratum, the cumulative 4-year incidence of the primary endpoint was significantly lower in the 4 mg than in the 1 mg group (4.0% and 4.9%, P=0.02), whereas in the intermediate- and high-risk strata, it was numerically lower in the 4 mg than in the 1 mg group. There was no significant treatment-by-subgroup interaction for the primary endpoint (P-interaction=0.77).
High-dose pitavastatin therapy compared with low-dose pitavastatin therapy was associated with a trend toward lowering the risk for cardiovascular events irrespective of the thrombotic risk in patients with CCS.
目前尚不清楚对于慢性冠脉综合征(CCS)患者,较高剂量他汀类药物对心血管事件的有益影响是否因血栓形成风险而异。
随机评估积极或中等强度降脂治疗与匹伐他汀在冠心病中的作用(REAL-CAD)研究是一项比较 CCS 患者 4 mg 和 1 mg 匹伐他汀的随机试验。本研究根据 CREDO-Kyoto 血栓形成风险评分将 12413 例患者分为 3 个亚组:低危(N=9434;4 mg:N=4742,1 mg:N=4692)、中危(N=2415;4 mg:N=1188,1 mg:N=1227)和高危(N=564;4 mg:N=269,1 mg:N=295)。主要终点为心血管死亡、非致死性心肌梗死、非致死性缺血性卒中和不稳定型心绞痛的复合终点。高危亚组的 4 年累积主要终点发生率明显高于中危和低危亚组(11.0%、6.3%和 4.5%,P<0.0001)。在低危亚组中,4 mg 组的 4 年累积主要终点发生率明显低于 1 mg 组(4.0%和 4.9%,P=0.02),而在中危和高危亚组中,4 mg 组的发生率低于 1 mg 组,但无统计学差异。主要终点的治疗-亚组交互作用无统计学意义(P 交互=0.77)。
与低剂量匹伐他汀治疗相比,高剂量匹伐他汀治疗与降低 CCS 患者心血管事件风险呈趋势相关,而与血栓形成风险无关。