Abstract

To quantitatively assess the distribution pattern of hippocampal tau pathology in Alzheimer’s disease (AD) and primary age-related tauopathy (PART), we investigated the distribution of phosphorylated tau protein (AT8) in 6 anatomically defined subregions of the hippocampal formation and developed a mathematical algorithm to compare the patterns of tau deposition in PART and AD. We demonstrated regional patterns of selective vulnerability as distinguishing features of PART and AD in functionally relevant structures of the hippocampus. In AD cases, tau pathology was high in both CA1 and subiculum, followed by CA2/3, entorhinal cortex (EC), CA4, and dentate gyrus (DG). In PART, the severity of tau pathology in CA1 and subiculum was high, followed by EC, CA2/3, CA4, and DG. There are significant differences between sector DG and CA1, DG and subiculum in both AD and PART.

Highlights

  • To quantitatively assess the distribution pattern of hippocampal tau pathology in Alzheimer’s disease (AD) and primary agerelated tauopathy (PART), we investigated the distribution of phosphorylated tau protein (AT8) in 6 anatomically defined subregions of the hippocampal formation and developed a mathematical algorithm to compare the patterns of tau deposition in PART and AD

  • It remains a debate whether PART is a subtype of AD or a distinct tauopathy different from AD (Duyckaerts et al 2015; Jellinger et al 2015)

  • We investigated the distribution of phosphorylated tau protein (AT8) in 6 anatomically defined subregions of the hippocampal formation and developed a mathematical algorithm to compare the patterns of tau deposition in PART and AD

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Summary

Introduction

To quantitatively assess the distribution pattern of hippocampal tau pathology in Alzheimer’s disease (AD) and primary agerelated tauopathy (PART), we investigated the distribution of phosphorylated tau protein (AT8) in 6 anatomically defined subregions of the hippocampal formation and developed a mathematical algorithm to compare the patterns of tau deposition in PART and AD. 2 Department of Pathology, Zhejiang University School of Medicine, Hangzhou 310058, China The hippocampus is an early region demonstrating tau pathology in both PART and AD.

Results
Conclusion

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