4.5 Article

Frontal Cortex Neuropathology in Dementia Pugilistica

期刊

JOURNAL OF NEUROTRAUMA
卷 29, 期 6, 页码 1054-1070

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2011.1957

关键词

beta-amyloid; C1q; chronic traumatic encephalopathy; tauopathy; TDP-43

资金

  1. University of California Irvine Alzheimer' Disease Research Center (National Institutes on Health/National Institutes on Aging) [P50 AG16573]
  2. National Institutes on Health/National Institutes on Aging [AG21912, AG00538]
  3. University of Kentucky Alzheimer's Disease Center [P30 AG028383]
  4. National Institute of Child Health and Human Development Brain [N01-HD-4-3368, N01-HD-4-3383]

向作者/读者索取更多资源

Dementia pugilistica (DP) is associated with chronic traumatic brain injury (CTBI), and leads to a punch drunk'' syndrome characterized by impairments in memory and executive function, behavioral changes, and motor signs. Microscopic features include the accumulation of neurofibrillary tangles (NFTs), beta-amyloid (A beta), and TAR DNA binding protein 43 (TDP-43) pathology. Here we describe detailed clinical and neuropathological data about a 55-year-old retired boxer (ApoE3/4), who presented with executive dysfunction and behavioral impairments. At autopsy, significant A beta pathology was seen, primarily in the form of diffuse plaques. Tau pathology was extensive and was determined to be of Braak and Braak stage VI. Frontal white matter showed evidence of glial tau inclusions (astrocytes and oligodendroglia). Cerebrovascular pathology was minimal with patchy amyloid angiopathy. Inflammation was another key feature, including microglial activation and significant C1q labeling of neurons, along with NFTs. TDP-43-positive pathology was also observed. Inflammation may be a key inciting as well as propagating feature of DP neuropathology.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据