Department of Cardiology (M.Y., Y.Y., S.-L.D., F.Y., Y.-F.Y., Y.-H.L., S.-L.H., K.L., F.W., X.C.), Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hubei Key Laboratory of Biological Targeted Therapy (M.Y., Y.Y., S.-L.D., F.Y., Y.-F.Y., Y.-H.L., S.-L.H., K.L., F.W., X.C.), Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Circulation. 2024 Sep 24;150(13):981-993. doi: 10.1161/CIRCULATIONAHA.124.069808. Epub 2024 Aug 21.
Colchicine has been approved to reduce cardiovascular risk in patients with coronary heart disease on the basis of its potential benefits demonstrated in the COLCOT (Colchicine Cardiovascular Outcomes Trial) and LoDoCo2 (Low-Dose Colchicine 2) studies. Nevertheless, there are limited data available about the specific impact of colchicine on coronary plaques.
This was a prospective, single-center, randomized, double-blind clinical trial. From May 3, 2021, until August 31, 2022, a total of 128 patients with acute coronary syndrome aged 18 to 80 years with lipid-rich plaque (lipid pool arc >90°) detected by optical coherence tomography were included. The subjects were randomly assigned in a 1:1 ratio to receive either colchicine (0.5 mg once daily) or placebo for 12 months. The primary end point was the change in the minimal fibrous cap thickness from baseline to the 12-month follow-up.
Among 128 patients, 52 in the colchicine group and 52 in the placebo group completed the study. The mean age of the 128 patients was 58.0±9.8 years, and 25.0% were female. Compared with placebo, colchicine therapy significantly increased the minimal fibrous cap thickness (51.9 [95% CI, 32.8 to 71.0] μm versus 87.2 [95% CI, 69.9 to 104.5] μm; difference, 34.2 [95% CI, 9.7 to 58.6] μm; =0.006), and reduced average lipid arc (-25.2° [95% CI, -30.6° to -19.9°] versus -35.7° [95% CI, -40.5° to -30.8°]; difference, -10.5° [95% CI, -17.7° to -3.4°]; =0.004), mean angular extension of macrophages (-8.9° [95% CI, -13.3° to -4.6°] versus -14.0° [95% CI, -18.0° to -10.0°]; difference, -6.0° [95% CI, -11.8° to -0.2°]; =0.044), high-sensitivity C-reactive protein level (geometric mean ratio, 0.6 [95% CI, 0.4 to 1.0] versus 0.3 [95% CI, 0.2 to 0.5]; difference, 0.5 [95% CI, 0.3 to 1.0]; =0.046), interleukin-6 level (geometric mean ratio, 0.8 [95% CI, 0.6 to 1.1] versus 0.5 [95% CI, 0.4 to 0.7]; difference, 0.6 [95% CI, 0.4 to 0.9]; =0.025), and myeloperoxidase level (geometric mean ratio, 1.0 [95% CI, 0.8 to 1.2] versus 0.8 [95% CI, 0.7 to 0.9]; difference, 0.8 [95% CI, 0.6 to 1.0]; =0.047).
Our findings suggested that colchicine resulted in favorable effects on coronary plaque stabilization at optical coherence tomography in patients with acute coronary syndrome.
URL: https://www.clinicaltrials.gov; Unique identifier: NCT04848857.
基于 COLCOT(秋水仙碱心血管结局试验)和 LoDoCo2(低剂量秋水仙碱 2 )研究中显示的潜在益处,秋水仙碱已被批准用于降低冠心病患者的心血管风险。然而,关于秋水仙碱对冠状动脉斑块的具体影响,数据有限。
这是一项前瞻性、单中心、随机、双盲临床试验。从 2021 年 5 月 3 日至 2022 年 8 月 31 日,共纳入 128 例年龄在 18 至 80 岁之间、经光学相干断层扫描(OCT)检测为富含脂质斑块(脂质池弧>90°)的急性冠状动脉综合征患者。将患者按 1:1 的比例随机分配,分别接受秋水仙碱(0.5mg,每日 1 次)或安慰剂治疗 12 个月。主要终点是从基线到 12 个月随访时最小纤维帽厚度的变化。
在 128 例患者中,52 例接受秋水仙碱治疗,52 例接受安慰剂治疗,共有 128 例患者完成了研究。患者的平均年龄为 58.0±9.8 岁,25.0%为女性。与安慰剂相比,秋水仙碱治疗组最小纤维帽厚度显著增加(51.9[95%CI,32.8 至 71.0]μm 与 87.2[95%CI,69.9 至 104.5]μm;差值,34.2[95%CI,9.7 至 58.6]μm;=0.006),平均脂质弧(-25.2°[95%CI,-30.6°至-19.9°]与 -35.7°[95%CI,-40.5°至-30.8°];差值,-10.5°[95%CI,-17.7°至-3.4°];=0.004)、巨噬细胞平均角延伸(-8.9°[95%CI,-13.3°至-4.6°]与 -14.0°[95%CI,-18.0°至-10.0°];差值,-6.0°[95%CI,-11.8°至-0.2°];=0.044)、高敏 C 反应蛋白水平(几何均数比值,0.6[95%CI,0.4 至 1.0]与 0.3[95%CI,0.2 至 0.5];差值,0.5[95%CI,0.3 至 1.0];=0.046)、白细胞介素-6 水平(几何均数比值,0.8[95%CI,0.6 至 1.1]与 0.5[95%CI,0.4 至 0.7];差值,0.6[95%CI,0.4 至 0.9];=0.025)和髓过氧化物酶水平(几何均数比值,1.0[95%CI,0.8 至 1.2]与 0.8[95%CI,0.7 至 0.9];差值,0.8[95%CI,0.6 至 1.0];=0.047)。
我们的研究结果表明,秋水仙碱在 OCT 检查中对急性冠状动脉综合征患者的冠状动脉斑块稳定具有有利作用。