Asymmetry of Hippocampal Tau Pathology in Primary Age-Related Tauopathy and Alzheimer Disease

Author:

Walker Jamie M12,Fudym Yelena34,Farrell Kurt567,Iida Megan A5678,Bieniek Kevin F129,Seshadri Sudha21011,White Charles L12,Crary John F567,Richardson Timothy E132

Affiliation:

1. From the Department of Pathology and Laboratory Medicine, Upstate Medical University, Syracuse, New York, USA

2. Glenn Biggs Institute for Alzheimer’s & Neurodegenerative Diseases, University of Texas Health Science Center, San Antonio, Texas, USA

3. Department of Pathology, State University of New York, Upstate Medical University, Syracuse, New York, USA

4. Department of Pathology, University of Michigan, Ann Arbor, Michigan, USA

5. Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, New York, USA

6. Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA

7. Ronald M. Loeb Center for Alzheimer’s Disease, Icahn School of Medicine at Mount Sinai, New York, New York, USA

8. School of Medicine, University of Michigan, Ann Arbor, Michigan, USA

9. Department of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA

10. Department of Neurology, University of Texas Health Science Center, San Antonio, Texas, USA

11. The Framingham Heart Study, Framingham, Massachusetts, USA

12. Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA

Abstract

Abstract Primary age-related tauopathy (PART) is a neurodegenerative entity defined as neurofibrillary degeneration generally restricted to the medial temporal region (Braak stage I–IV) with complete or near absence of diffuse and neuritic plaques. Symptoms range in severity but are generally milder and later in onset than in Alzheimer disease (AD). Recently, an early predilection for neurofibrillary degeneration in the hippocampal CA2 subregion has been demonstrated in PART, whereas AD neuropathologic change (ADNC) typically displays relative sparing of CA2 until later stages. In this study, we utilized a semiquantitative scoring system to evaluate asymmetry of neurofibrillary degeneration between left and right hippocampi in 67 PART cases and 17 ADNC cases. 49% of PART cases demonstrated asymmetric findings in at least one hippocampal subregion, and 79% of the asymmetric cases displayed some degree of CA2 asymmetry. Additionally, 19% of cases revealed a difference in Braak score between the right and left hippocampi. There was a significant difference in CA2 neurofibrillary degeneration (p = 0.0006) and CA2/CA1 ratio (p < 0.0001) when comparing the contralateral sides, but neither right nor left was more consistently affected. These data show the importance of analyzing bilateral hippocampi in the diagnostic evaluation of PART and potentially of other neurodegenerative diseases.

Funder

National Institute on Aging

NIA

National Institutes of Health

Alzheimer’s Association

Tau Consortium

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

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