Journal of Stroke & Cerebrovascular Diseases ( IF 2.5 ) Pub Date : 2021-08-26 , DOI: 10.1016/j.jstrokecerebrovasdis.2021.106068 Daniel Schranz 1 , Tihamer Molnar 2 , Szabina Erdo-Bonyar 3 , Diana Simon 3 , Tímea Berki 3 , Laszlo Zavori 4 , Alex Szolics 5 , Andras Buki 6 , Gabor Lenzser 6 , Peter Csecsei 6
Background
Aneurysmal subarachnoid hemorrhage (aSAH) is associated with activation of the inflammatory cascade contributing to unfavorable outcome and secondary complications, such as delayed cerebral ischemia (DCI). Both fatty acid–binding protein 3 (FABP3) and CXC-chemokine ligand 16 (CXCL-16) have been linked to vascular inflammation and cellular death. The authors aimed to assess the 30-day prognostic value of serum levels of FABP3 and CXCL-16 and explore their associations with DCI in aSAH patients.
Methods
A total of 60 patients with aSAH were prospectively enrolled. Sampling for markers was done at 24 hours after the index event. FABP3 and CXCL-16 serum concentrations were determined by MilliPlex multiplex immunoassay method. The primary endpoint was unfavorable outcome at Day 30 based on the modified Rankin Scale.
Results
Both FABP3 and CXCL-16 levels were significantly elevated in patients with unfavorable outcome compared to those with favorable outcome after aSAH (FABP3: 2133 pg/mL, IQR: 1053-4567 vs. 3773, 3295-13116; p<0.003 and CXCL-16: 384 pg/mL, 313-502 vs. 498, 456-62, p<0.001). The area under the curve (AUC) for serum CXCL-16 levels as a predictor of unfavorable outcome at Day 30 was 0.747 (95% CI =0.622-0.871; p<0.001). Based on binary logistic regression analysis, serum CXCL-16 with a cut-off level >446.7 ng/L independently predicted Day 30 unfavorable outcome with a sensitivity of 81% and a specificity of 62%. Neither CXCL-16 nor FABP3 showed a significant correlation with DCI.
Conclusion
Early FABP3 and CXCL-16 levels are significantly associated with poor 30-day outcome in patients with aSAH.
中文翻译:
脂肪酸结合蛋白 3 和 CXC-趋化因子配体 16 与动脉瘤性蛛网膜下腔出血的不良结局相关
背景
动脉瘤性蛛网膜下腔出血 (aSAH) 与炎症级联反应的激活有关,导致不良结果和继发性并发症,例如迟发性脑缺血 (DCI)。脂肪酸结合蛋白 3 (FABP3) 和 CXC-趋化因子配体 16 (CXCL-16) 都与血管炎症和细胞死亡有关。作者旨在评估 FABP3 和 CXCL-16 血清水平的 30 天预后价值,并探讨它们与 aSAH 患者中 DCI 的关联。
方法
共有 60 名 aSAH 患者被前瞻性纳入。在指标事件后 24 小时进行标记物采样。FABP3 和 CXCL-16 血清浓度通过 MilliPlex 多重免疫测定法测定。主要终点是第 30 天基于改良 Rankin 量表的不利结果。
结果
与 aSAH 后预后良好的患者相比,预后不良的患者的 FABP3 和 CXCL-16 水平均显着升高(FABP3:2133 pg/mL,IQR:1053-4567 vs. 3773、3295-13116;p<0.003 和 CXCL- 16:384 pg/mL,313-502 对比 498、456-62,p<0.001)。作为第 30 天不利结果的预测因子的血清 CXCL-16 水平的曲线下面积 (AUC) 为 0.747(95% CI = 0.622-0.871;p<0.001)。基于二元逻辑回归分析,具有 >446.7 ng/L 临界值的血清 CXCL-16 独立预测第 30 天不利结果,敏感性为 81%,特异性为 62%。CXCL-16 和 FABP3 均未显示出与 DCI 的显着相关性。
结论
早期 FABP3 和 CXCL-16 水平与 aSAH 患者的 30 天预后不良显着相关。