德国美式足球运动员在一个赛季中重复性头部受伤不会改变 CTE 的血液生物标志物候选者。

Q2 Medicine
Theres Bastgen, Janis Evers, Christiane Oedekoven, Caroline Weide, Lars Herzog, Nicholas Ashton, Henrik Zetterberg, Kaj Blennow, Alexandra Albus, Natasha Vidovic, Oliver Kraff, Cornelius Deuschl, Richard Dodel, J Alexander Ross
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引用次数: 0

摘要

背景:美式橄榄球运动员(AFP)的重复性脑外伤可导致神经退行性疾病慢性创伤性脑病(CTE)。CTE 的临床症状包括情绪和行为变化、认知障碍、抑郁和自杀。迄今为止,CTE 尚无法在体内诊断,因此需要找到 CTE 的特定诊断参数,以便尽早观察和治疗暴露的运动员。有前景的 CTE 血液生物标志物包括总 tau(tTau)、高磷酸化 tau(pTau)、神经丝蛋白(NF-L)、神经胶质纤维酸性蛋白(GFAP)、淀粉样蛋白-β40(Aβ40)、淀粉样蛋白-β42(Aβ42)和钙结合蛋白 B(S100-B)。先前的研究发现,这些生物标志物在受到创伤性脑损伤的受试者中水平升高,而在 CTE 受试者中,Aβ40 和 Aβ42 的脑脊液(CSF)水平降低。在此,我们研究了年轻的 AFPs 在单个活跃季节是否已经表现出这些候选生物标志物的变化:方法:在一个完整赛季之前和之后,从 n = 18 名美式足球运动员和 n = 18 名年龄匹配的男性对照组受试者身上抽取血样。测定血浆中 tTau、pTau、NF-L、GFAP、Aβ40、Aβ42 和 S100-B 的滴度。此外,还对冷漠、抑郁和健康状况以及脑震荡病史和医疗护理进行了评估和相关分析:结果:我们在此表明,与健康对照组相比,所选的 CTE 候选生物标志物在美式足球单个活跃赛季的七个月期间,在 AFPs 血液样本中并无明显变化。但有趣的是,他们的 pTau 滴度普遍升高。此外,我们还发现抑郁、生活质量、职业生涯长度、训练参与度和训练持续时间与不同滴度的脑震荡后头痛存在相关性:我们的数据表明,CTE 标志物候选者的变化要么在美式足球的几个活跃赛季中缓慢发生,要么只在脑脊液中发现。尽管如此,我们的研究结果还是强调了对这些候选生物标志物进行长期评估的重要性,这在未来有可能通过重复监测暴露运动员的血液生物标志物来实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Repetitive head injuries in German American football players do not change blood-based biomarker candidates for CTE during a single season.

Background: Repetitive traumatic brain injuries in American football players (AFPs) can lead to the neurodegenerative disease chronic traumatic encephalopathy (CTE). Clinical symptoms of CTE range from mood and behavioral changes to cognitive impairment, depression, and suicidality. So far, CTE cannot be diagnosed in vivo and thus specific diagnostic parameters for CTE need to be found, to observe and treat exposed athletes as early as possible. Promising blood-based biomarkers for CTE include total tau (tTau), hyperphosphorylated tau (pTau), neurofilament light protein (NF-L), glial fibrillary acidic protein (GFAP), amyloid-β40 (Aβ40), amyloid-β42 (Aβ42) and calcium-binding protein B (S100-B). Previous studies have found elevated levels of these biomarkers in subjects exposed to TBIs, whereas cerebrospinal fluid (CSF) levels of Aβ40 and Aβ42 were decreased in CTE subjects. Here, we investigated whether young AFPs already exhibit changes of these biomarker candidates during the course of a single active season.

Methods: Blood samples were drawn from n = 18 American Football Players before and after a full season and n = 18 male age-matched control subjects. The plasma titers of tTau, pTau, NF-L, GFAP, Aβ40, Aβ42 and S100-B were determined. Additionally, Apathy, Depression, and Health status as well as the concussion history and medical care were assessed and analyzed for correlations.

Results: Here we show, that the selected biomarker candidates for CTE do not change significantly during the seven-month period of a single active season of American Football in blood samples of AFPs compared to healthy controls. But interestingly, they exhibit generally elevated pTau titers. Furthermore, we found correlations of depression, quality-of-life, career length, training participation and training continuation with headache after concussion with various titers.

Conclusion: Our data indicates, that changes of CTE marker candidates either occur slowly over several active seasons of American Football or are exclusively found in CSF. Nevertheless, our results underline the importance of a long-term assessment of these biomarker candidates, which might be possible through repeated blood biomarker monitoring in exposed athletes in the future.

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