Clinical Department, Banyan Biomarkers, Inc., Alachua, FL, USA.
Neurology. 2013 Apr 30;80(18):1662-8. doi: 10.1212/WNL.0b013e3182904d43. Epub 2013 Apr 3.
The study aims to examine α-synuclein in the CSF of patients with severe traumatic brain injury (TBI) and its relationship with clinical characteristics and long-term outcomes.
This prospective case-control study enrolled patients with severe TBI (Glasgow Coma Score ≤ 8) who underwent ventriculostomy. CSF samples were taken from each TBI patient at admission and daily for up to 8 days after injury and successively assessed by ELISA. Control CSF was collected for analysis from subjects receiving lumbar puncture for other medical reasons. We used trajectory analysis to identify distinct temporal profiles of CSF α-synuclein that were compared with clinical outcomes.
CSF α-synuclein was elevated in TBI patients after injury as compared to controls (p = 0.0008). Overall, patients who died had higher concentrations (area under the curve) over 8 days of observation compared to those who survived at 6 months postinjury (p = 0.002). Two distinct temporal α-synuclein profiles were recognized over time. Subjects who died had consistently elevated α-synuclein levels compared to those who survived with α-synuclein levels near controls. High-risk trajectory was a strong and accurate predictor of death with 100% specificity and a very high sensitivity (83%).
Taken together, these data support the hypothesis that in severe TBI patients, substantial increase of CSF α-synuclein may indicate widespread neurodegeneration and reflect secondary neuropathologic events occurring after injury. The determination of CSF α-synuclein may be a valuable prognostic marker, adding to the clinical assessment and creating opportunities for medical intervention.
本研究旨在探讨严重创伤性脑损伤(TBI)患者脑脊液(CSF)中的α-突触核蛋白及其与临床特征和长期预后的关系。
这项前瞻性病例对照研究纳入了接受脑室引流术的严重 TBI 患者(格拉斯哥昏迷评分≤8)。在损伤后每天采集每位 TBI 患者的 CSF 样本,连续通过 ELISA 进行评估。对照组 CSF 样本取自因其他医学原因接受腰椎穿刺的受试者。我们使用轨迹分析来识别 CSFα-突触核蛋白的不同时间特征,并与临床结局进行比较。
与对照组相比,TBI 患者损伤后 CSFα-突触核蛋白升高(p=0.0008)。总体而言,与伤后 6 个月存活的患者相比,死亡患者在 8 天观察期内的浓度(曲线下面积)更高(p=0.002)。随着时间的推移,我们识别出了两种不同的 CSFα-突触核蛋白时间特征。与存活患者相比,死亡患者的α-突触核蛋白水平持续升高,而存活患者的α-突触核蛋白水平接近对照组。高危轨迹是死亡的有力且准确预测指标,特异性为 100%,灵敏度非常高(83%)。
综上所述,这些数据支持了以下假设:在严重 TBI 患者中,CSFα-突触核蛋白的大量增加可能表明广泛的神经退行性变,并反映损伤后发生的继发性神经病理事件。CSFα-突触核蛋白的测定可能是一种有价值的预后标志物,可补充临床评估,并为医学干预创造机会。