McCabe John J, Harris Katie, Walsh Cathal, Gorey Sarah, Arnold Markus, De Marchis Gian Marco, Hervella Pablo, Iglesias-Rey Ramon, Jern Christina, Katan Mira, Li Linxin, Miyamoto Nobukazu, Montaner Joan, Purroy Francisco, Rothwell Peter M, Stanne Tara M, Sudlow Cathie, Ueno Yuji, Vicente-Pascual Mikel, Whiteley William, Woodward Mark, Kelly Peter J
Health Research Board (HRB) Stroke Clinical Trials Network Ireland (SCTNI) (J.J.M., C.W., S.G., P.J.K.).
School of Medicine, University College Dublin (UCD), Ireland (J.J.M., S.G., P.J.K.).
Stroke. 2025 Sep;56(9):2588-2596. doi: 10.1161/STROKEAHA.125.052091. Epub 2025 Jul 18.
Uncertainty remains whether inflammation is implicated in poststroke recurrence in patients without atherosclerosis. We evaluated the contribution of atherosclerosis status to the association between inflammatory markers and major adverse cardiovascular events (MACE) poststroke.
We performed an individual-participant data meta-analysis of 11 prospective cohorts (12 countries, 1995-2017). Studies included patients with ischemic stroke/transient ischemic attack and measured IL (interleukin)-6/hsCRP (high-sensitivity C-reactive protein) postevent. We analyzed the association between IL-6/hsCRP and recurrent stroke/MACE using multivariable Cox regression analyses (conditional logistic regression for 1 study). Analyses were stratified by the presence/absence of atherosclerosis (definition: prior history of coronary disease, peripheral artery disease, or large artery atherosclerotic stroke) and adjusted for cardiovascular risk factors/preventative medication.
Overall 10 148 patients (3448 [34.0%] had atherosclerosis) with 21 177 years of follow-up were included (1707 MACE outcomes/1353 recurrent strokes). In patients with atherosclerosis, IL-6 was independently associated with MACE (risk ratio [RR], 1.22 [95% CI, 1.08-1.37]; per logunit increase) and recurrent stroke (RR, 1.23 [95% CI, 1.08-1.41]). Compared with patients in the bottom quarter, those in the top quarter of IL-6 levels had double the risk of MACE (RR, 2.05 [95% CI, 1.37-3.08]) and stroke (RR, 1.97 [95% CI, 1.28-3.05]). IL-6 was also associated with MACE (RR, 1.11 [95% CI, 1.01-1.23]) but not stroke (RR, 1.08 [95% CI, 0.98-1.20]; per logunit) in patients without atherosclerosis. However, there was no evidence of statistical interaction between IL-6 levels and atherosclerosis status for either outcome (=0.25 and 0.13 for MACE/recurrent stroke, respectively). hsCRP was associated with MACE in patients with (RR, 1.12 [95% CI, 1.05-1.21]; per logunit) and without atherosclerosis (RR, 1.07 [95% CI, 1.01-1.14]; =0.28). No association with recurrent stroke was observed for hsCRP with (RR, 1.06 [95% CI, 0.98-1.14]) or without atherosclerosis (RR, 0.97 [95% CI, 0.91-1.04]; =0.18).
IL-6/hsCRP were associated with poststroke recurrence irrespective of atherosclerosis. These data support the inclusion of patients in trials of anti-inflammatory therapies after stroke with elevated IL-6 or hsCRP, including those without prior atherosclerotic events.
对于无动脉粥样硬化的患者,炎症是否与卒中后复发有关仍不确定。我们评估了动脉粥样硬化状态对炎症标志物与卒中后主要不良心血管事件(MACE)之间关联的影响。
我们对11个前瞻性队列(12个国家,1995 - 2017年)进行了个体参与者数据荟萃分析。研究纳入了缺血性卒中/短暂性脑缺血发作患者,并在事件发生后测量了白细胞介素(IL)-6/高敏C反应蛋白(hsCRP)。我们使用多变量Cox回归分析(1项研究采用条件逻辑回归)分析了IL-6/hsCRP与复发性卒中/MACE之间的关联。分析按有无动脉粥样硬化(定义:冠心病、外周动脉疾病或大动脉粥样硬化性卒中的既往史)进行分层,并对心血管危险因素/预防性用药进行了调整。
共纳入10148例患者(3448例[34.0%]有动脉粥样硬化),随访21177人年(1707例MACE结局/1353例复发性卒中)。在有动脉粥样硬化的患者中,IL-6与MACE(风险比[RR],1.22[95%CI,1.08 - 1.37];每增加一个对数单位)和复发性卒中(RR,1.23[95%CI,1.08 - 1.41])独立相关。与IL-6水平处于最低四分位数的患者相比,处于最高四分位数的患者发生MACE的风险加倍(RR,2.05[95%CI,1.37 - 3.08])和卒中的风险加倍(RR,1.97[95%CI,1.28 - 3.05])。在无动脉粥样硬化的患者中,IL-6也与MACE相关(RR,1.11[95%CI,1.01 - 1.23]),但与卒中无关(RR,1.08[95%CI,0.98 -