| Literature DB >> 36004533 |
Kurt Farrell1, Megan A Iida1, Jonathan D Cherry2,3,4, Alicia Casella1, Thor D Stein2,3,4, Kevin F Bieniek5,6, Jamie M Walker5,6, Timothy E Richardson5,6, Charles L White7, Victor E Alvarez2,3,4,8, Bertrand R Huber2,3,4,8, Dennis W Dickson9, Ricardo Insausti10, Kristen Dams-O'Connor11, Ann C McKee2,3,4,8, John F Crary1.
Abstract
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.Entities:
Keywords: Aging; Chronic traumatic encephalopathy; Primary age-related tauopathy; Repetitive head impacts; Tauopathy
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Year: 2022 PMID: 36004533 PMCID: PMC9487677 DOI: 10.1093/jnen/nlac066
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.148