Molnar Tihamer, Borocz Kata, Berki Timea, Szapary Laszlo, Szolics Alex, Janszky Jozsef, Illes Zsolt, Csecsei Peter
Department of Anaesthesiology and Intensive Care, University of Pecs, Pecs, Hungary.
Department of Immunology and Biotechnology, University of Pecs, Pecs, Hungary.
J Stroke Cerebrovasc Dis. 2019 Mar;28(3):719-727. doi: 10.1016/j.jstrokecerebrovasdis.2018.11.015. Epub 2018 Dec 5.
Caspase-cleaved cytokeratin-18 (CCCK-18) is an apoptosis marker. Here, we analyzed the relationship between plasma level of CCCK-18 in the acute and subacute stage of ischemic stroke and early and late functional outcome. Besides, correlation among CCCK-18 and complications, such as hemorrhagic transformation (HT) were also explored.
Plasma concentration of CCCK-18 was investigated in 54 patients at admission and poststroke 72 hours. HT was evaluated by CT scans on 24 poststroke hours. Outcome measures were assessed by modified Rankin scale at hospital discharge and 6-month later. Receiver operating characteristics (ROC) analysis was used to determine the best cut-off values of CCCK-18 as a predictor of unfavorable functional outcome.
Significantly elevated CCCK-18 level was observed at 72 hours after onset of stroke, in nonsurviving compared to surviving patients (331 ± 191 ng/L versus 251 ± 164 ng/L, P = .01). Based on ROC analysis, the cut-off value of plasma CCCK-18 levels >223 ng/L at 72 poststroke hours predicted 6-month unfavorable stroke outcome with a sensitivity of 84.4% and a specificity of 77.3% (area under the curve: .851, 95% confidence interval = .745-.955, P < .001). The rate of complications such as HT and in-hospital infection was significantly higher in patients presented with a plasma CCCK-18 level above the cut-off value.
The association between high serum CCCK-18 levels and unfavorable early and late stroke outcome in an unselected study population was first described here. Besides, the apoptosis marker CCCK-18 might be a predictor of further complication such as HT and in-hospital infection.
半胱天冬酶切割的细胞角蛋白18(CCCK-18)是一种凋亡标志物。在此,我们分析了缺血性中风急性和亚急性期血浆CCCK-18水平与早期和晚期功能结局之间的关系。此外,还探讨了CCCK-18与出血性转化(HT)等并发症之间的相关性。
对54例患者入院时及卒中后72小时的血浆CCCK-18浓度进行了研究。通过卒中后24小时的CT扫描评估HT。出院时及6个月后采用改良Rankin量表评估结局指标。采用受试者工作特征(ROC)分析确定CCCK-18作为不良功能结局预测指标的最佳截断值。
与存活患者相比,卒中发作后72小时未存活患者的CCCK-18水平显著升高(331±191 ng/L对251±164 ng/L,P = 0.01)。基于ROC分析,卒中后72小时血浆CCCK-18水平>223 ng/L的截断值预测6个月时不良卒中结局的敏感性为84.4%,特异性为77.3%(曲线下面积:0.851,95%置信区间=0.745 - 0.955,P < 0.001)。血浆CCCK-18水平高于截断值的患者发生HT和院内感染等并发症的发生率显著更高。
本研究首次描述了在未选择的研究人群中高血清CCCK-18水平与早期和晚期不良卒中结局之间的关联。此外,凋亡标志物CCCK-18可能是HT和院内感染等进一步并发症的预测指标。