Department of Neurosurgery, The Affiliated Lihuili Hospital of Ningbo University, Ningbo, Zhejiang, China.
Department of Neurosurgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China.
CNS Neurosci Ther. 2024 Sep;30(9):e70009. doi: 10.1111/cns.70009.
Traumatic brain injury (TBI) remains a major concern for global health. Recent studies have suggested the role of NOD-like receptor pyrin domain-containing protein 3 (NLRP3), an inflammatory marker, in the cerebrospinal fluid (CSF) and serum as potential indicators of TBI prognosis. The objective of the study was to characterize NLRP3 as a clinically applicable tool for predicting the outcomes of TBI patients.
A total of 270 patients with moderate to severe TBI were included in this retrospective analysis. Serum and CSF samples were collected at 1-, 3-, 7-, and 21-day post-injury to measure NLRP3 levels. The prognosis of patients was evaluated after 3 months using the Glasgow Outcome Scale (GOS). Patients were categorized into good prognosis (GOS score >3) and poor prognosis (GOS score ≤3) groups. The relationship between NLRP3 levels and prognosis was analyzed.
Patients with poor prognosis had significantly elevated NLRP3 levels in their serum on days 1 and 3 post-injury compared with those with a good prognosis. The difference was more pronounced during these early days compared with days 7 and 21. However, NLRP3 levels in CSF consistently showed a large difference between the two groups throughout the observation period. Receiver operating characteristic analysis revealed that the level of NLRP3 in the CSF on day 3 post-injury had the highest predictive value for prognosis, with an area under the curve of 0.83, followed by the level of NLRP3 in the serum on day 3 post-injury.
The levels of NLRP3, especially in the CSF on day 3 post-injury, can serve as a potential biomarker for predicting prognosis in moderate to severe TBI patients. Early measurement of NLRP3 levels can provide valuable insights into patient outcomes and guide therapeutic strategies.
创伤性脑损伤(TBI)仍然是全球健康的主要关注点。最近的研究表明,NOD 样受体富含吡咯烷域蛋白 3(NLRP3)作为炎症标志物,在脑脊液(CSF)和血清中的作用可能是 TBI 预后的潜在指标。本研究的目的是将 NLRP3 作为一种有临床应用价值的工具,用于预测 TBI 患者的预后。
本回顾性分析共纳入 270 例中重度 TBI 患者。在伤后 1、3、7 和 21 天采集血清和 CSF 样本,以测量 NLRP3 水平。3 个月后使用格拉斯哥结局量表(GOS)评估患者的预后。将患者分为预后良好(GOS 评分>3)和预后不良(GOS 评分≤3)两组。分析 NLRP3 水平与预后的关系。
与预后良好的患者相比,预后不良的患者伤后第 1 天和第 3 天血清 NLRP3 水平显著升高。在这些早期,与第 7 天和第 21 天相比,差异更为明显。然而,整个观察期间,两组患者 CSF 中 NLRP3 水平始终存在较大差异。受试者工作特征曲线分析显示,伤后第 3 天 CSF 中 NLRP3 水平对预后的预测价值最高,曲线下面积为 0.83,其次是伤后第 3 天血清 NLRP3 水平。
NLRP3 水平,特别是伤后第 3 天 CSF 中的 NLRP3 水平,可能成为预测中重度 TBI 患者预后的潜在生物标志物。早期测量 NLRP3 水平可以为患者结局提供有价值的信息,并指导治疗策略。