Penn Center for Brain Injury and Repair and Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, 105 Hayden Hall, 3320 Smith Walk, Philadelphia, PA 19104, USA.
Nat Rev Neurol. 2013 Apr;9(4):211-21. doi: 10.1038/nrneurol.2013.29. Epub 2013 Mar 5.
Traumatic brain injury (TBI) has long been recognized to be a risk factor for dementia. This association has, however, only recently gained widespread attention through the increased awareness of 'chronic traumatic encephalopathy' (CTE) in athletes exposed to repetitive head injury. Originally termed 'dementia pugilistica' and linked to a career in boxing, descriptions of the neuropathological features of CTE include brain atrophy, cavum septum pellucidum, and amyloid-β, tau and TDP-43 pathologies, many of which might contribute to clinical syndromes of cognitive impairment. Similar chronic pathologies are also commonly found years after just a single moderate to severe TBI. However, little consensus currently exists on specific features of these post-TBI syndromes that might permit their confident clinical and/or pathological diagnosis. Moreover, the mechanisms contributing to neurodegeneration following TBI largely remain unknown. Here, we review the current literature and controversies in the study of chronic neuropathological changes after TBI.
创伤性脑损伤(TBI)长期以来一直被认为是痴呆的一个危险因素。然而,正是由于人们对运动员反复头部受伤导致的“慢性创伤性脑病”(CTE)的认识不断提高,这种关联才引起了广泛关注。CTE 最初被称为“拳击痴呆症”,与拳击生涯有关,其神经病理学特征包括脑萎缩、透明隔腔、淀粉样β、tau 和 TDP-43 病理学,其中许多可能导致认知障碍的临床综合征。即使只有一次中度至重度 TBI,多年后也会出现类似的慢性病变。然而,目前对于这些 TBI 后综合征的特定特征还没有达成共识,这些特征可能会使其得到明确的临床和/或病理诊断。此外,TBI 后导致神经退行性变的机制在很大程度上仍不清楚。在这里,我们回顾了 TBI 后慢性神经病理学变化研究的现有文献和争议。