- Main
Differential Vulnerability of Hippocampal Subfields in Primary Age-Related Tauopathy and Chronic Traumatic Encephalopathy.
- Farrell, Kurt;
- Iida, Megan A;
- Cherry, Jonathan D;
- Casella, Alicia;
- Stein, Thor D;
- Bieniek, Kevin F;
- Walker, Jamie M;
- Richardson, Timothy E;
- White, Charles L;
- Alvarez, Victor E;
- Huber, Bertrand R;
- Dickson, Dennis W;
- Insausti, Ricardo;
- Dams-O'Connor, Kristen;
- Vonsattel, Jean-Paul;
- Teich, Andy F;
- Gearing, Marla;
- Glass, Jonathan;
- Troncoso, Juan C;
- Frosch, Matthew P;
- Hyman, Bradley T;
- Murray, Melissa E;
- Attems, Johannes;
- Flanagan, Margaret E;
- Mao, Qinwen;
- Mesulam, M-Marsel;
- Weintraub, Sandra;
- Woltjer, Randy L;
- Pham, Thao;
- Kofler, Julia;
- Schneider, Julie A;
- Yu, Lei;
- Purohit, Dushyant P;
- Haroutunian, Vahram;
- Hof, Patrick R;
- Gandy, Sam;
- Sano, Mary;
- Beach, Thomas G;
- Poon, Wayne;
- Kawas, Claudia H;
- Corrada, María M;
- Rissman, Robert A;
- Metcalf, Jeff;
- Shuldberg, Sara;
- Salehi, Bahar;
- Nelson, Peter T;
- Trojanowski, John Q;
- Lee, Edward B;
- Wolk, David A;
- McMillan, Corey T;
- Keene, C Dirk;
- Latimer, Caitlin S;
- Montine, Thomas J;
- Kovacs, Gabor G;
- Lutz, Mirjam I;
- Fischer, Peter;
- Perrin, Richard J;
- Cairns, Nigel J;
- McKee, Ann C;
- Crary, John F
- et al.
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.
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