Department of Clinical Sciences Lund, Neurosurgery, Lund University, Lund, Sweden.
Department of Neuroscience, Neurosurgery, Uppsala University, Uppsala, Sweden.
J Neuroinflammation. 2023 Aug 17;20(1):189. doi: 10.1186/s12974-023-02864-0.
A sports-related concussion (SRC) is often caused by rapid head rotation at impact, leading to shearing and stretching of axons in the white matter and initiation of secondary inflammatory processes that may exacerbate the initial injury. We hypothesized that athletes with persistent post-concussive symptoms (PPCS) display signs of ongoing neuroinflammation, as reflected by altered profiles of cerebrospinal fluid (CSF) biomarkers, in turn relating to symptom severity. We recruited athletes with PPCS preventing sports participation as well as limiting work, school and/or social activities for ≥ 6 months for symptom rating using the Sport Concussion Assessment Tool, version 5 (SCAT-5) and for cognitive assessment using the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). Following a spinal tap, we analysed 27 CSF inflammatory biomarkers (pro-inflammatory chemokines and cytokine panels) by a multiplex immunoassay using antibodies as electrochemiluminescent labels to quantify concentrations in PPCS athletes, and in healthy age- and sex-matched controls exercising ≤ 2 times/week at low-to-moderate intensity. Thirty-six subjects were included, 24 athletes with PPCS and 12 controls. The SRC athletes had sustained a median of five concussions, the most recent at a median of 17 months prior to the investigation. CSF cytokines and chemokines levels were significantly increased in eight (IL-2, TNF-α, IL-15, TNF-β, VEGF, Eotaxin, IP-10, and TARC), significantly decreased in one (Eotaxin-3), and unaltered in 16 in SRC athletes when compared to controls, and two were un-detectable. The SRC athletes reported many and severe post-concussive symptoms on SCAT5, and 10 out of 24 athletes performed in the impaired range (Z < - 1.5) on cognitive testing. Individual biomarker concentrations did not strongly correlate with symptom rating or cognitive function. Limitations include evaluation at a single post-injury time point in relatively small cohorts, and no control group of concussed athletes without persisting symptoms was included. Based on CSF inflammatory marker profiling we find signs of ongoing neuroinflammation persisting months to years after the last SRC in athletes with persistent post-concussive symptoms. Since an ongoing inflammatory response may exacerbate the brain injury these results encourage studies of treatments targeting the post-injury inflammatory response in sports-related concussion.
运动相关性脑震荡(SRC)通常是由于头部在撞击时快速旋转,导致白质中的轴突发生剪切和拉伸,并引发继发性炎症过程,从而加重初始损伤。我们假设持续性脑震荡后症状(PPCS)运动员表现出持续的神经炎症迹象,这反映在脑脊液(CSF)生物标志物的改变模式中,进而与症状严重程度相关。我们招募了因持续性脑震荡后症状而无法参加运动、限制工作、学业和/或社交活动≥6 个月的运动员,使用运动性脑震荡评估工具第 5 版(SCAT-5)进行症状评分,并使用重复神经心理状态评估测试(RBANS)进行认知评估。在进行腰椎穿刺后,我们使用多聚免疫分析法分析了 27 种 CSF 炎症生物标志物(促炎趋化因子和细胞因子谱),该方法使用电化学发光标记的抗体来定量 PPCS 运动员和每周运动≤2 次、运动强度为低到中等的健康年龄和性别匹配对照者的 CSF 中浓度。共纳入 36 名受试者,其中 24 名 SRC 运动员和 12 名对照者。SRC 运动员中位发生了 5 次脑震荡,最近一次发生在调查前的中位时间为 17 个月。与对照组相比,SRC 运动员的 CSF 细胞因子和趋化因子水平显著升高了 8 种(IL-2、TNF-α、IL-15、TNF-β、VEGF、Eotaxin、IP-10 和 TARC),显著降低了 1 种(Eotaxin-3),16 种未改变,2 种未检出。SRC 运动员在 SCAT5 上报告了许多和严重的脑震荡后症状,24 名运动员中有 10 名在认知测试中表现出受损(Z<−1.5)。单个生物标志物浓度与症状评分或认知功能没有很强的相关性。局限性包括在相对较小的队列中仅在受伤后单一时间点进行评估,并且没有包括持续存在症状的非持续性脑震荡运动员的对照组。基于 CSF 炎症标志物分析,我们发现,在有持续性脑震荡后症状的运动员中,在最后一次 SRC 后数月至数年内存在持续的神经炎症迹象。由于持续的炎症反应可能会加重脑损伤,因此这些结果鼓励研究针对运动相关性脑震荡的受伤后炎症反应的治疗方法。