Mckee Ann C, Abdolmohammadi Bobak, Stein Thor D
VA Boston Healthcare System, Boston, MA, United States; Departments of Neurology and Pathology, Boston University School of Medicine, and Boston University CTE Center, Boston, MA, United States.
Departments of Neurology and Pathology, Boston University School of Medicine, and Boston University CTE Center, Boston, MA, United States.
Handb Clin Neurol. 2018;158:297-307. doi: 10.1016/B978-0-444-63954-7.00028-8.
Chronic traumatic encephalopathy (CTE) is a neurodegenerative tauopathy associated with repetitive head trauma, including concussion and subconcussion. CTE was first recognized in boxers nearly a century ago as "dementia pugilistica" or "punch drunk," but has been recently identified in contact sports athletes (including American football, ice hockey, soccer, baseball, rugby, boxing, and wrestling) and military veterans exposed to blast. Similar to many other neurodegenerative diseases, CTE is diagnosed conclusively only by neuropathologic examination of brain tissue. CTE is characterized by the buildup of hyperphosphorylated tau as neurofibrillary tangles, abnormal neurites, and inclusions in astrocytes around small blood vessels with a tendency to occur in clusters at the sulcal depths of the cortex. Using the McKee criteria, a consensus panel of expert neuropathologists confirmed CTE as a unique neurodegenerative disease with a pathognomonic CTE lesion that has only been found in individuals exposed to brain trauma. Recently, 177 instances of CTE were reported in a convenience sample of 202 former American football players, including 110 of 111 former National Football League players (99%), 48 of 53 former college football players (91%), and 3 of 14 former high school players (21%), by far the largest case series ever reported. Significant increases in active microglia and inflammation also occur after repetitive head impact injury and in CTE. A preliminary study showed that inflammatory cytokines were elevated in the brain tissue and cerebrospinal fluid of individuals with pathologically confirmed CTE compared to controls and individuals with Alzheimer disease, which may some day be useful in diagnosis of CTE during life. Although many fundamental questions remain to be answered regarding CTE, postmortem analysis of tissue from brain donors and tissue-based research have accelerated and expanded our current understanding of CTE and its pathogenesis. Guided by the neuropathologic findings, current research efforts are underway to develop biomarkers to diagnose CTE and effective ways to treat the disorder during life.
慢性创伤性脑病(CTE)是一种与重复性头部创伤相关的神经退行性tau蛋白病,包括脑震荡和亚脑震荡。CTE近一个世纪前在拳击手中首次被确认为“拳击性痴呆”或“拳击醉酒”,但最近在接触性运动运动员(包括美式橄榄球、冰球、足球、棒球、橄榄球、拳击和摔跤)以及遭受爆炸冲击的退伍军人中也被发现。与许多其他神经退行性疾病一样,CTE只有通过脑组织的神经病理学检查才能最终确诊。CTE的特征是过度磷酸化的tau蛋白堆积形成神经原纤维缠结、异常神经突以及小血管周围星形胶质细胞中的包涵体,且倾向于在皮质沟深处成簇出现。使用麦基标准,专家神经病理学家共识小组确认CTE是一种独特的神经退行性疾病,具有仅在遭受脑外伤的个体中发现的特征性CTE病变。最近,在202名前美式橄榄球运动员的便利样本中报告了177例CTE病例,其中包括111名前美国国家橄榄球联盟球员中的110例(99%)、53名前大学橄榄球运动员中的48例(91%)以及14名前高中球员中的3例(21%),这是迄今为止报告的最大病例系列。重复性头部撞击损伤后以及CTE患者中还会出现活跃小胶质细胞和炎症的显著增加。一项初步研究表明,与对照组以及阿尔茨海默病患者相比,经病理证实患有CTE的个体的脑组织和脑脊液中炎症细胞因子水平升高,这可能有朝一日有助于生前诊断CTE。尽管关于CTE仍有许多基本问题有待解答,但对脑捐赠者组织的死后分析和基于组织的研究加速并扩展了我们目前对CTE及其发病机制的理解。在神经病理学发现的指导下,目前正在进行研究以开发诊断CTE的生物标志物以及在生前治疗该疾病的有效方法。