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血清GFAP和UCH-L1水平用于评估无出血转化:一项多中心前瞻性队列研究

Serum GFAP and UCH-L1 Levels for the Assessment of the Absence of Hemorrhagic Transformation: A Multicenter Prospective Cohort Study.

作者信息

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

机构信息

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.

出版信息

Stroke. 2025 Jan;56(1):22-29. doi: 10.1161/STROKEAHA.124.047887. Epub 2024 Dec 9.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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%)。

结论

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。

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