Department of Vascular Medicine, University Medical Centre Utrecht, Utrecht, The Netherlands.
Department of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Eur J Prev Cardiol. 2023 Dec 21;30(18):1950-1962. doi: 10.1093/eurjpc/zwad221.
Low-dose colchicine reduces cardiovascular risk in patients with coronary artery disease (CAD), but absolute benefits may vary between individuals. This study aimed to assess the range of individual absolute benefits from low-dose colchicine according to patient risk profile.
The European Society of Cardiology (ESC) guideline-recommended SMART-REACH model was combined with the relative treatment effect of low-dose colchicine and applied to patients with CAD from the Low-Dose Colchicine 2 (LoDoCo2) trial and the Utrecht Cardiovascular Cohort-Second Manifestations of ARTerial disease (UCC-SMART) study (n = 10 830). Individual treatment benefits were expressed as 10-year absolute risk reductions (ARRs) for myocardial infarction, stroke, or cardiovascular death (MACE), and MACE-free life-years gained. Predictions were also performed for MACE plus coronary revascularization (MACE+), using a new lifetime model derived in the REduction of Atherothrombosis for Continued Health (REACH) registry. Colchicine was compared with other ESC guideline-recommended intensified (Step 2) prevention strategies, i.e. LDL cholesterol (LDL-c) reduction to 1.4 mmol/L and systolic blood pressure (SBP) reduction to 130 mmHg. The generalizability to other populations was assessed in patients with CAD from REACH North America and Western Europe (n = 25 812). The median 10-year ARR from low-dose colchicine was 4.6% [interquartile range (IQR) 3.6-6.0%] for MACE and 8.6% (IQR 7.6-9.8%) for MACE+. Lifetime benefit was 2.0 (IQR 1.6-2.5) MACE-free years, and 3.4 (IQR 2.6-4.2) MACE+-free life-years gained. For LDL-c and SBP reduction, respectively, the median 10-year ARR for MACE was 3.0% (IQR 1.5-5.1%) and 1.7% (IQR 0.0-5.7%), and the lifetime benefit was 1.2 (IQR 0.6-2.1) and 0.7 (IQR 0.0-2.3) MACE-free life-years gained. Similar results were obtained for MACE+ and in American and European patients from REACH.
The absolute benefits of low-dose colchicine vary between individual patients with chronic CAD. They may be expected to be of at least similar magnitude to those of intensified LDL-c and SBP reduction in a majority of patients already on conventional lipid-lowering and blood pressure-lowering therapy.
小剂量秋水仙碱可降低冠心病(CAD)患者的心血管风险,但个体的绝对获益可能有所不同。本研究旨在根据患者的风险状况评估小剂量秋水仙碱的个体绝对获益范围。
将欧洲心脏病学会(ESC)指南推荐的 SMART-REACH 模型与小剂量秋水仙碱的相对治疗效果相结合,并应用于来自低剂量秋水仙碱 2 期(LoDoCo2)试验和乌得勒支心血管队列-动脉疾病第二次表现(UCC-SMART)研究的 CAD 患者(n=10830)。个体治疗获益表示为心肌梗死、卒中和心血管死亡(MACE)的 10 年绝对风险降低(ARR),以及 MACE 无病生存年限的增加。还使用在 REduction of Atherothrombosis for Continued Health(REACH)登记处中获得的新的终生模型,对 MACE 加冠状动脉血运重建(MACE+)进行了预测。将秋水仙碱与 ESC 指南推荐的强化(第 2 步)预防策略(即 LDL 胆固醇(LDL-c)降低至 1.4mmol/L 和收缩压(SBP)降低至 130mmHg)进行比较。在来自 REACH 北美和西欧的 CAD 患者(n=25812)中评估了其在其他人群中的通用性。在接受小剂量秋水仙碱治疗的患者中,中位 10 年 MACE 的 ARR 为 4.6%(IQR 3.6-6.0%),MACE+的 ARR 为 8.6%(IQR 7.6-9.8%)。终生获益为 2.0(IQR 1.6-2.5)个 MACE 无病生存年限,3.4(IQR 2.6-4.2)个 MACE+-无病生存年限。对于 LDL-c 和 SBP 降低,MACE 的中位 10 年 ARR 分别为 3.0%(IQR 1.5-5.1%)和 1.7%(IQR 0.0-5.7%),终生获益为 1.2(IQR 0.6-2.1)和 0.7(IQR 0.0-2.3)个 MACE 无病生存年限。在接受 LDL-c 和 SBP 降低治疗的患者中,MACE+和来自 REACH 的美国和欧洲患者也得到了类似的结果。
慢性 CAD 患者的小剂量秋水仙碱的绝对获益因人而异。预计在大多数已接受常规降脂和降压治疗的患者中,其获益幅度至少与强化 LDL-c 和 SBP 降低的获益幅度相似。