Escalera Erica, Saver Jeffrey L
David Geffen School of Medicine, University of California, Los Angeles, CA USA.
Comprehensive Stroke Center and Department of Neurology, Ronald Reagan - UCLA Medical Center, Los Angeles, CA USA.
J Stroke Cerebrovasc Dis. 2025 Feb;34(2):108186. doi: 10.1016/j.jstrokecerebrovasdis.2024.108186. Epub 2024 Dec 10.
As the Food and Drug Administration in June 2023 approved low dose colchicine for primary prevention of stroke and other cardiovascular events, an updated meta-analysis of stroke outcomes in randomized trials would help inform clinical practice.**** METHODS: Systematic, study-level meta-analysis of randomized clinical trials of long-term colchicine in patients with established atherosclerotic cardiovascular disease (ASCVD, preponderantly primary prevention for stroke) or following non-cardioembolic ischemic stroke/transient ischemic attack (secondary prevention). Heterogeneity was assessed with the I statistic and Cochrane's Q and potential bias assessed with the Risk of Bias 2.0 scale.
Six randomized control trials met selection criteria, enrolling 14,987 patients (7495 colchicine, 7492 placebo), with median follow-up 26.3 months. Colchicine dosage in all trials was 0.5 mg once-daily. Across all trials, colchicine treatment produced a 28 % relative risk reduction in stroke (1.77 % vs 2.54 %, risk ratio (RR)=0.72, 95 %CI: 0.58-0.89; p = 0.003) and a comparable relative reduction on major adverse cardiovascular events. There was potential heterogeneity by subgroup (p = 0.06), with a stronger relative reduction for stroke in the five ASCVD trials (RR=0.48, 95 %CI:0.30-0.77; p = 0.003) than the non-cardioembolic ischemic stroke/TIA population (RR=0.80, 95 %CI:0.63-1.02; p = 0.07). Colchicine was associated with a small, non-significant increase in all-cause mortality (RR: 1.09; 95 %Cl: 0.85-1.40, p = 0.49) but not cardiovascular death (RR: 0.92; 95 %Cl: 0.65-1.29, p = 0.61).
Low-dose colchicine treatment decreases stroke and major adverse cardiovascular event risk in patients with ASCVD and potentially in patients following a non-cardioembolic ischemic stroke/TIA. Among every 1000 patients treated over 2 years, approximately 6.6 strokes and 24 major adverse cardiovascular events are avoided.
由于美国食品药品监督管理局于2023年6月批准低剂量秋水仙碱用于中风和其他心血管事件的一级预防,对随机试验中的中风结局进行更新的荟萃分析将有助于为临床实践提供参考。
对已确诊动脉粥样硬化性心血管疾病(ASCVD,主要为中风一级预防)患者或非心源性缺血性中风/短暂性脑缺血发作后(二级预防)长期使用秋水仙碱的随机临床试验进行系统的、研究水平的荟萃分析。使用I统计量和Cochrane's Q评估异质性,使用偏倚风险2.0量表评估潜在偏倚。
六项随机对照试验符合入选标准,纳入14987例患者(7495例秋水仙碱组,7492例安慰剂组),中位随访时间为26.3个月。所有试验中秋水仙碱剂量均为每日一次0.5毫克。在所有试验中,秋水仙碱治疗使中风的相对风险降低28%(1.77%对2.54%,风险比(RR)=0.72,95%置信区间:0.58 - 0.89;p = 0.003),主要不良心血管事件的相对降低幅度相当。亚组间存在潜在异质性(p = 0.06),在五项ASCVD试验中中风的相对降低幅度更强(RR = 0.48,95%置信区间:0.30 - 0.77;p = 0.003),高于非心源性缺血性中风/短暂性脑缺血发作人群(RR = 0.80,95%置信区间:0.63 - 1.02;p = 0.07)。秋水仙碱与全因死亡率的小幅非显著性增加相关(RR:1.09;95%置信区间:0.85 - 1.40,p = 0.49),但与心血管死亡无关(RR:0.92;95%置信区间:0.65 - 1.29,p = 0.61)。
低剂量秋水仙碱治疗可降低ASCVD患者以及可能非心源性缺血性中风/短暂性脑缺血发作患者的中风和主要不良心血管事件风险。在两年内接受治疗的每1000例患者中,大约可避免6.6例中风和24例主要不良心血管事件。