Nicks Raymond, Shah Arsal, Stathas Spiro Anthony, Kirsch Daniel, Horowitz Sarah M, Saltiel Nicole, Calderazzo Samantha M, Butler Morgane L M D, Cormier Kerry A, Aytan Nurgul, Tu-Zahra Fatima, Mathias Rebecca, Faheem Farwa, Marcus Suzie, Spurlock Elizabeth, Fishbein Lucas, Esnault Camille D, Boden Alexandra, Rosen Grace, Xia Weiming, Daley Sarah, Meng Gaoyuan, Martin Brett R, Daneshvar Daniel H, Nowinski Christopher J, Alosco Michael L, Mez Jesse, Tripodis Yorghos, Huber Bertrand R, Alvarez Victor E, Cherry Jonathan D, McKee Ann C, Stein Thor D
Boston University Alzheimer's Disease and CTE Center, Boston Chobanian & Avedisian University School of Medicine, Boston, MA, USA.
VA Boston Healthcare System, Boston, MA, USA.
Acta Neuropathol. 2024 Dec 6;148(1):79. doi: 10.1007/s00401-024-02833-8.
Neurodegeneration is a seminal feature of many neurological disorders. Chronic traumatic encephalopathy (CTE) is caused by repetitive head impacts (RHI) and is characterized by sulcal tau pathology. However, quantitative assessments of regional neurodegeneration in CTE have not been described. In this study, we quantified three key neurodegenerative measures, including cortical thickness, neuronal density, and synaptic proteins, in contact sport athletes (n = 185) and non-athlete controls (n = 52) within the sulcal depth, middle, and gyral crest of the dorsolateral frontal cortex. Cortical thickness and neuronal density were decreased within the sulcus in CTE compared to controls (p's < 0.05). Measurements of synaptic proteins within the gyral crest showed a reduction of α-synuclein with CTE stage (p = 0.002) and variable changes in PSD-95 density. After adjusting for age, multiple linear regression models demonstrated a strong association between the duration of contact sports play and cortical thinning (p = 0.001) and neuronal loss (p = 0.032) within the sulcus. Additional regression models, adjusted for tau pathology, suggest that within the sulcus, the duration of play was associated with neuronal loss predominantly through tau pathology. In contrast, the association of duration of play with cortical thinning was minimally impacted by tau pathology. Overall, CTE is associated with cortical atrophy and a predominant sulcal neurodegeneration. Furthermore, the duration of contact sports play is associated with measures of neurodegeneration that are more severe in the cortical sulcus and may occur through tau-dependent and independent mechanisms.
神经退行性变是许多神经系统疾病的一个关键特征。慢性创伤性脑病(CTE)由重复性头部撞击(RHI)引起,其特征为脑沟内tau蛋白病变。然而,尚未有对CTE中区域神经退行性变的定量评估报道。在本研究中,我们对185名从事接触性运动的运动员和52名非运动员对照者背外侧前额叶皮质脑沟深度、中部和脑回嵴处的三项关键神经退行性变指标进行了量化,包括皮质厚度、神经元密度和突触蛋白。与对照组相比,CTE患者脑沟内的皮质厚度和神经元密度降低(p值<0.05)。脑回嵴处突触蛋白的测量显示,α-突触核蛋白随CTE分期减少(p = 0.002),而突触后致密蛋白95(PSD-95)密度有不同变化。在调整年龄后,多元线性回归模型显示接触性运动的持续时间与脑沟内皮质变薄(p = 0.001)和神经元丢失(p = 0.032)之间存在强关联。经tau蛋白病变调整的其他回归模型表明,在脑沟内,运动持续时间与神经元丢失的关联主要通过tau蛋白病变介导。相比之下,运动持续时间与皮质变薄的关联受tau蛋白病变的影响最小。总体而言,CTE与皮质萎缩和主要的脑沟神经退行性变相关。此外,接触性运动的持续时间与神经退行性变指标相关,这些指标在皮质脑沟处更为严重,可能通过tau蛋白依赖和非依赖机制发生。