Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, United States; Department of Biomedical Engineering, Medical College of Wisconsin, Milwaukee, WI, United States; Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, United States.
Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Brain Behav Immun. 2021 Jan;91:531-540. doi: 10.1016/j.bbi.2020.11.011. Epub 2020 Nov 8.
The molecular mechanisms underlying the diverse psychiatric and neuropathological sequalae documented in subsets of athletes with concussion have not been identified. We have previously reported elevated quinolinic acid (QuinA), a neurotoxic kynurenine pathway metabolite, acutely following concussion in football players with prior concussion. Similarly, work from our group and others has shown that increased functional connectivity strength, assessed using resting state fMRI, occurs following concussion and is associated with worse concussion-related symptoms and outcome. Moreover, other work has shown that repetitive concussion may have cumulative effects on functional connectivity and is a risk factor for adverse outcomes. Understanding the molecular mechanisms underlying these cumulative effects may ultimately be important for therapeutic interventions or the development of prognostic biomarkers. Thus, in this work, we tested the hypothesis that the relationship between QuinA in serum and functional connectivity following concussion would depend on the presence of a prior concussion. Concussed football players with prior concussion (N = 21) and without prior concussion (N = 16) completed a MRI session and provided a blood sample at approximately 1 days, 8 days, 15 days, and 45 days post-injury. Matched, uninjured football players with (N = 18) and without prior concussion (N = 24) completed similar visits. The association between QuinA and global connectivity strength differed based on group (F(3, 127) = 3.46, p = 0.019); post-hoc analyses showed a positive association between QuinA and connectivity strength in concussed athletes with prior concussion (B = 16.05, SE = 5.06, p = 0.002, 95%CI[6.06, 26.03]), but no relationship in concussed athletes without prior concussion or controls. Region-specific analyses showed that this association was strongest in bilateral orbitofrontal cortices, insulae, and basal ganglia. Finally, exploratory analyses found elevated global connectivity strength in concussed athletes with prior concussion who reported depressive symptoms at the 1-day visit compared to those who did not report depressive symptoms (t(15) = 2.37, mean difference = 13.50, SE = 5.69, p = 0.032, 95%CI[1.36, 25.63], Cohen's d = 1.15.). The results highlight a potential role of kynurenine pathway (KP) metabolites in altered functional connectivity following concussion and raise the possibility that repeated concussion has a "priming" effect on KP metabolism.
在有脑震荡病史的运动员中,有多种精神和神经病理学后遗症,但目前尚未明确其潜在的分子机制。我们之前曾报道过,在有脑震荡病史的足球运动员中,急性脑震荡后会出现升高的犬尿氨酸途径代谢产物喹啉酸(QuinA)。同样,我们组和其他组的工作表明,静息态 fMRI 评估的功能连接强度增强会在脑震荡后发生,并且与更严重的脑震荡相关症状和结果相关。此外,其他研究表明,重复脑震荡可能对功能连接产生累积影响,并且是不良结果的危险因素。了解这些累积效应的潜在分子机制对于治疗干预或预后生物标志物的开发可能最终很重要。因此,在这项工作中,我们检验了以下假设:血清中 QuinA 与脑震荡后功能连接之间的关系取决于先前是否有脑震荡。有脑震荡病史的脑震荡足球运动员(N=21)和没有脑震荡病史的足球运动员(N=16)在受伤后约 1 天、8 天、15 天和 45 天进行 MRI 检查并采集血液样本。有脑震荡病史的匹配、未受伤的足球运动员(N=18)和无脑震荡病史的匹配、未受伤的足球运动员(N=24)进行了类似的就诊。QuinA 与整体连接强度之间的关系因组而异(F(3,127)=3.46,p=0.019);事后分析显示,在有脑震荡病史的运动员中,QuinA 与连接强度呈正相关(B=16.05,SE=5.06,p=0.002,95%CI[6.06,26.03]),但在无脑震荡病史的运动员或对照组中没有关系。区域特异性分析表明,这种关联在双侧眶额皮质、岛叶和基底节最强。最后,探索性分析发现,在有脑震荡病史且在第 1 天就诊时报告有抑郁症状的运动员中,整体连接强度升高,而那些没有报告抑郁症状的运动员则没有(t(15)=2.37,平均差异=13.50,SE=5.69,p=0.032,95%CI[1.36,25.63],Cohen's d=1.15)。研究结果突出了犬尿氨酸途径(KP)代谢产物在脑震荡后功能连接改变中的潜在作用,并提出了重复脑震荡对 KP 代谢具有“启动”作用的可能性。