Departments of Pathology, Artificial Intelligence & Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank & Research CoRE, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Department of Pathology, Alzheimer's Disease and CTE Center, Boston University School of Medicine, Boston, Massachusetts, USA.
J Neuropathol Exp Neurol. 2022 Sep 19;81(10):781-789. doi: 10.1093/jnen/nlac066.
Chronic traumatic encephalopathy (CTE) is a tauopathy associated with repetitive mild head impacts characterized by perivascular hyperphosphorylated tau (p-tau) in neurofibrillary tangles (NFTs) and neurites in the depths of the neocortical sulci. In moderate to advanced CTE, NFTs accumulate in the hippocampus, potentially overlapping neuroanatomically with primary age-related tauopathy (PART), an age-related tauopathy characterized by Alzheimer disease-like tau pathology in the hippocampus devoid of amyloid plaques. We measured p-tau burden using positive-pixel counts on immunohistochemically stained and neuroanatomically segmented hippocampal tissue. Subjects with CTE had a higher total p-tau burden than PART subjects in all sectors (p = 0.005). Within groups, PART had significantly higher total p-tau burden in CA1/subiculum compared to CA3 (p = 0.02) and CA4 (p = 0.01) and total p-tau burden in CA2 trended higher than CA4 (p = 0.06). In CTE, total p-tau burden in CA1/subiculum was significantly higher than in the dentate gyrus; and CA2 also trended higher than dentate gyrus (p = 0.01, p = 0.06). When controlling for p-tau burden across the entire hippocampus, CA3 and CA4 had significantly higher p-tau burden in CTE than PART (p < 0.0001). These data demonstrate differences in hippocampal p-tau burden and regional distribution in CTE compared to PART that might be helpful in differential diagnosis and reveal insights into disease pathogenesis.
慢性创伤性脑病(CTE)是一种与反复轻度头部撞击相关的tau 病,其特征是神经纤维缠结(NFTs)和新皮质脑沟深部神经突内的血管周围过度磷酸化的 tau(p-tau)。在中度至晚期 CTE 中,NFTs 在海马体中积累,可能与原发性年龄相关性 tau 病(PART)在神经解剖学上重叠,后者是一种以海马体中阿尔茨海默病样 tau 病理学为特征的年龄相关性 tau 病,而无淀粉样斑块。我们使用免疫组织化学染色和神经解剖分割的海马组织上的阳性像素计数来测量 p-tau 负担。与 PART 受试者相比,CTE 受试者在所有区域的总 p-tau 负担都更高(p=0.005)。在组内,PART 在 CA1/下托比 CA3(p=0.02)和 CA4(p=0.01)的总 p-tau 负担显著更高,而 CA2 的总 p-tau 负担比 CA4 更高(p=0.06)。在 CTE 中,CA1/下托的总 p-tau 负担明显高于齿状回;而 CA2 也比齿状回更高(p=0.01,p=0.06)。在控制整个海马体的 p-tau 负担后,CA3 和 CA4 的 CTE 比 PART 的 p-tau 负担显著更高(p<0.0001)。这些数据表明,与 PART 相比,CTE 中海马体的 p-tau 负担和区域分布存在差异,这可能有助于鉴别诊断,并揭示疾病发病机制的见解。