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Metcalf, Jeff

https://orcid.org/0009-0007-2428-9856

Mayo Clinic

No affiliation available

Citations 1

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. , Richardson, Timothy E. , Alvarez, Victor E., Huber, Bertrand R. , Insausti, Ricardo , Group, The Part Working, Vonsattel, Jean‐Paul, Teich, Andy F, Gearing, Marla , Glass, Jonathan D. , Troncoso, Juan C. , Frosch, Matthew P. , Attems, Johannes , Mesulam, M-Marsel, Weıntraub, Sandra , Woltjer, Randy, Pham, Thao, Kofler, Julia , Yu, Lei , Purohit, Dushyant P. , Haroutunian, Vahram , Sano, Mary , Beach, Thomas G. , Kawas, Claudia H. , Metcalf, Jeff , Shuldberg, Sara, Salehi, Bahar , Nelson, Peter T. , Trojanowski, John Q. , Latimer, Caitlin S. , Montine, Thomas J. , Kovács, Gábor G. , Lutz, Mirjam I. , Perrin, Richard J. , Cairns, Nigel J. , McKee, Ann C. , Crary, John F. , Kovacs, Gabor G , Farrell, Kurt , Walker, Jamie M. , White, Charles L. , Dickson, Dennis W. , Dams-O’Connor, Kristen , Group, The Part Working, Teich, Andy F, Hyman, Bradley T. , Murray, Melissa E. , Flanagan, Margaret E. , Mao, Qinwen , Schneider, Julie A. , Yu, Lei , Hof, Patrick R. , Gandy, Sam , Poon, Wayne W. , Corrada, María M. , Rissman, Robert A. , Lee, Edward B. , Wolk, David A. , McMillan, Corey T. , Keene, C. Dirk , Fischer, Peter A.

Journal of Neuropathology & Experimental Neurology | August 25, 2022 | Volume: 81 | Issue: 10 | Pages: 781-789

10.1093/jnen/nlac066 Get It

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.