From the Department of Neurology (H. Liu, J.J., A.W., Q.X., X.M., H. Li, Z.L., Y.W.), Beijing Tiantan Hospital, Capital Medical University; China National Clinical Research Center for Neurological Diseases (H. Liu, J.J., A.W., Q.X., X.M., H. Li, Z.L., Y.W.), Beijing; and Department of Neurology and Suzhou Clinical Research Center of Neurological Disease (H. Liu), the Second Affiliated Hospital of Soochow University, China.
Neurology. 2023 Apr 18;100(16):e1643-e1654. doi: 10.1212/WNL.0000000000206775. Epub 2023 Jan 25.
Single small subcortical infarction (SSSI) is an important stroke subtype. The optimal antiplatelet medication for patients with ischemic stroke with an SSSI is still unclear. We aimed to test the efficacy and safety of ticagrelor-aspirin in preventing stroke recurrence among patients with SSSI in the Ticagrelor or Clopidogrel with Aspirin in High-Risk Patients with Acute Nondisabling Cerebrovascular Events II (CHANCE-2) trial.
In the CHANCE-2 trial, patients with a minor stroke or TIA who carried loss-of-function (LOF) alleles were randomly assigned within 24 hours after symptom onset, to either ticagrelor-aspirin (placebo clopidogrel plus a 180 mg loading dose of ticagrelor on day 1, followed by 90 mg twice daily on days 2-90) or clopidogrel-aspirin (placebo ticagrelor plus a 300 mg loading dose of clopidogrel on day 1, followed by 75 mg daily on days 2-90). Aspirin was applied during the first 21 days. Patients who had an SSSI (diffusion-weighted imaging lesion diameter ≤20 mm) were included in this analysis and further categorized into 2 types according to whether they had the responsible intracranial artery stenosis (ICAS): SSSI + ICAS and SSSI - ICAS. The primary efficacy outcome was a new stroke at 90 days.
Among 2,143 eligible patients, 340 had the responsible ICAS, and 1,803 did not. Ticagrelor-aspirin reduced stroke recurrence among all patients with SSSI (hazard ratio [HR]: 0.55; 95% CI 0.38-0.78; = 0.001) compared with clopidogrel-aspirin. Stroke recurrence occurred in 35/901 (3.9%) patients with SSSI - ICAS on ticagrelor-aspirin and in 72/902 (8.0%) on clopidogrel-aspirin (hazard ratio [HR]: 0.45; 95% CI 0.29-0.68; < 0.001). In patients with SSSI + ICAS, the corresponding event rates were 14/176 (8.0%) and 13/164 (7.9%), respectively (HR: 1.20; 95% CI 0.45-3.23; = 0.71; for interaction = 0.08). The risk of severe or moderate bleeding only occurred in patients with SSSI - ICAS (5/901 [0.6%] vs 5/902 [0.6%]).
In this prespecified substudy, ticagrelor-aspirin was superior to clopidogrel-aspirin in reducing the risk of stroke at 90 days among patients with SSSI who carried LOF allele(s). Although there was no treatment-by-heterogeneous etiology interaction, a greater absolute risk reduction of stroke was observed in patients with SSSI - ICAS than in those with SSSI + ICAS.
This study provides Class II evidence that ticagrelor and aspirin reduced the risk of stroke recurrence compared with clopidogrel with aspirin in adult patients with acute minor SSSI.
单发小皮质下梗死(SSSI)是一种重要的卒中亚型。对于伴有 SSSI 的缺血性卒中患者,最佳的抗血小板药物仍不明确。我们旨在 CHANCE-2 试验中检验替格瑞洛-阿司匹林在预防 SSSI 患者卒中复发方面的疗效和安全性。
在 CHANCE-2 试验中,症状出现后 24 小时内,携带功能丧失(LOF)等位基因的小卒中和 TIA 患者被随机分为替格瑞洛-阿司匹林组(替格瑞洛安慰剂联合第 1 天 180mg 负荷剂量,第 2-90 天每天 90mg;21 天内给予阿司匹林)或氯吡格雷-阿司匹林组(氯吡格雷安慰剂联合第 1 天 300mg 负荷剂量,第 2-90 天每天 75mg;21 天内给予阿司匹林)。患者均于第 1 天接受替格瑞洛或氯吡格雷负荷剂量。本分析纳入了存在 SSSI(弥散加权成像病变直径≤20mm)的患者,并根据是否存在责任颅内动脉狭窄(ICAS)进一步分为 2 种类型:SSSI + ICAS 和 SSSI - ICAS。主要疗效终点为 90 天新发卒中。
在 2143 名合格患者中,340 名患者存在责任 ICAS,1803 名患者不存在。与氯吡格雷-阿司匹林相比,替格瑞洛-阿司匹林降低了所有 SSSI 患者的卒中复发风险(风险比[HR]:0.55;95%置信区间[CI]:0.38-0.78; = 0.001)。在 SSSI - ICAS 患者中,替格瑞洛-阿司匹林组发生卒中复发 35/901(3.9%),氯吡格雷-阿司匹林组为 72/902(8.0%)(HR:0.45;95%CI:0.29-0.68; < 0.001)。在 SSSI + ICAS 患者中,相应的事件发生率分别为 14/176(8.0%)和 13/164(7.9%)(HR:1.20;95%CI:0.45-3.23; = 0.71;交互检验=0.08)。严重或中度出血风险仅见于 SSSI - ICAS 患者(5/901 [0.6%] vs 5/902 [0.6%])。
在本预先设定的亚组研究中,替格瑞洛-阿司匹林降低了携带 LOF 等位基因的 SSSI 患者 90 天卒中风险,优于氯吡格雷-阿司匹林。虽然治疗与异质性病因之间无交互作用,但 SSSI - ICAS 患者的卒中绝对风险降低幅度大于 SSSI + ICAS 患者。
本研究提供了 II 级证据,表明替格瑞洛联合阿司匹林与氯吡格雷联合阿司匹林相比,降低了急性小 SSSI 成人患者的卒中复发风险。