Department of Pathology, Glenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases, UT Health San Antonio, San Antonio, Texas.
Department of Neurology, Washington University School of Medicine, Saint Louis, Missouri.
J Neuropathol Exp Neurol. 2021 Feb 22;80(3):210-219. doi: 10.1093/jnen/nlab001.
Chronic traumatic encephalopathy (CTE) is a neurodegenerative disorder associated with exposure to head trauma. In 2015, a panel of neuropathologists funded by the NINDS/NIBIB defined preliminary consensus neuropathological criteria for CTE, including the pathognomonic lesion of CTE as "an accumulation of abnormal hyperphosphorylated tau (p-tau) in neurons and astroglia distributed around small blood vessels at the depths of cortical sulci and in an irregular pattern," based on review of 25 tauopathy cases. In 2016, the consensus panel met again to review and refine the preliminary criteria, with consideration around the minimum threshold for diagnosis and the reproducibility of a proposed pathological staging scheme. Eight neuropathologists evaluated 27 cases of tauopathies (17 CTE cases), blinded to clinical and demographic information. Generalized estimating equation analyses showed a statistically significant association between the raters and CTE diagnosis for both the blinded (OR = 72.11, 95% CI = 19.5-267.0) and unblinded rounds (OR = 256.91, 95% CI = 63.6-1558.6). Based on the challenges in assigning CTE stage, the panel proposed a working protocol including a minimum threshold for CTE diagnosis and an algorithm for the assessment of CTE severity as "Low CTE" or "High CTE" for use in future clinical, pathological, and molecular studies.
慢性创伤性脑病(CTE)是一种与头部创伤暴露相关的神经退行性疾病。2015 年,由 NINDS/NIBIB 资助的一组神经病理学家定义了 CTE 的初步共识神经病理学标准,包括 CTE 的特征性病变,即“皮质沟深部小血管周围神经元和星形胶质细胞中异常高磷酸化 tau(p-tau)的积累,呈不规则模式”,这是基于对 25 例 tau 病病例的回顾。2016 年,共识小组再次开会审查和完善初步标准,考虑到诊断的最低阈值和拟议的病理分期方案的可重复性。八名神经病理学家对 27 例 tau 病病例(17 例 CTE 病例)进行了评估,对临床和人口统计学信息进行了盲法评估。广义估计方程分析显示,评分者与 CTE 诊断之间存在统计学显著关联,无论是盲法(OR=72.11,95%CI=19.5-267.0)还是非盲法(OR=256.91,95%CI=63.6-1558.6)。基于 CTE 分期分配的挑战,该小组提出了一个工作方案,包括 CTE 诊断的最低阈值和用于评估 CTE 严重程度的算法,即“低 CTE”或“高 CTE”,用于未来的临床、病理和分子研究。