Guo Zhen-Ni, Qu Yang, Abuduxukuer Reziya, Jin Hang, Zhang Peng, Wang Jing, Zhang Ke-Jia, Qi Shuang, Zheng Xiang-Yu, Zhang Yu, Gao Jian-Hua, Pan De-Wang, Liu Xiao-Dong, Li Chun-Ying, Chen Li-Ping, Chen Jin-Hua, Gu Ji-Liang, Wang An-Ying, Jiang Ligang, Liu Liang, Jiang Yongfei, Wang Chun-Fei, Jia Yan, Xin Hong, Jiang Chun-Li, Qi Ying-Bin, Hu Xue-Feng, Li Song, Sun Xin, Nguyen Thanh N, Yang Yi
Stroke Center, Department of Neurology (Z.-N.G., Y.Q., R.A., H.J., P.Z., J.W., K.-J.Z., S.Q., X.S., Y.Y.), The First Hospital of Jilin University, Changchun, China.
Neuroscience Research Center, Department of Neurology (Z.-N.G.), The First Hospital of Jilin University, Changchun, China.
Stroke. 2025 Jan;56(1):22-29. doi: 10.1161/STROKEAHA.124.047887. Epub 2024 Dec 9.
Currently, validated biomarkers for assessing hemorrhagic transformation (HT) after intravenous thrombolysis (IVT) are lacking. We aimed to validate a test combining GFAP (glial fibrillary acidic protein) and UCH-L1 (ubiquitin C-terminal hydrolase-L1) to indicate the absence of HT after IVT.
We prospectively enrolled consecutive patients with stroke treated with IVT from 16 hospitals. Serum GFAP and UCH-L1 levels were measured 24 hours after IVT. Cases from 1 hospital were randomly assigned to the training (70%) and testing (30%) cohorts for internal validation. The external validation cohort included patients from the other 15 hospitals. Cutoff levels of GFAP and UCH-L1 for assessing the absence of HT were established in the training cohort and subjected to internal and external verification.
A total of 1063 patients were included. Both GFAP and UCH-L1 levels were independently associated with HT, infarct volume, and 3-month outcome; levels lower than cutoff (12.6 and 63.1 pg/mL, respectively) excluded patients with HT with a negative predictive value of 98.31% (95% CI, 89.70%-99.91%) and detection sensitivity of 98.08% (95% CI, 88.42%-99.90%) in the training cohort. In the testing and validation cohorts, negative predictive value was 100% (95% CI, 75.93%-100%) and 100% (95% CI, 82.19%-100%), respectively, and the sensitivity was 100% (95% CI, 80.76%-100%) and 100% (95% CI, 77.08%-100%), respectively.
Serum GFAP and UCH-L1 levels exhibit high sensitivity and negative predictive value for indicating the absence of HT 24 hours after IVT, which supports their potential role in assessing patients' condition after IVT.
目前,缺乏用于评估静脉溶栓(IVT)后出血性转化(HT)的经过验证的生物标志物。我们旨在验证一种结合胶质纤维酸性蛋白(GFAP)和泛素羧基末端水解酶-L1(UCH-L1)的检测方法,以表明IVT后无HT。
我们前瞻性地纳入了来自16家医院接受IVT治疗的连续卒中患者。在IVT后24小时测量血清GFAP和UCH-L1水平。将1家医院的病例随机分配到训练队列(70%)和测试队列(30%)进行内部验证。外部验证队列包括来自其他15家医院的患者。在训练队列中确定用于评估无HT的GFAP和UCH-L1的临界值,并进行内部和外部验证。
共纳入1063例患者。GFAP和UCH-L1水平均与HT、梗死体积和3个月结局独立相关;低于临界值(分别为12.6和63.1 pg/mL)的水平排除了HT患者,在训练队列中阴性预测值为98.31%(95%CI,89.70%-99.91%),检测灵敏度为98.08%(95%CI,88.42%-99.90%)。在测试队列和验证队列中,阴性预测值分别为100%(95%CI,75.93%-100%)和100%(95%CI,82.19%-100%),灵敏度分别为100%(95%CI,80.76%-100%)和100%(95%CI,77.08%-100%)。
血清GFAP和UCH-L1水平在IVT后24小时表明无HT方面表现出高灵敏度和阴性预测值,这支持了它们在评估IVT后患者病情中的潜在作用。