Hemispheric Asymmetry and Atypical Lobar Progression of Alzheimer-Type Tauopathy

Author:

Tremblay Cécilia1ORCID,Serrano Geidy E1ORCID,Intorcia Anthony J1,Curry Jasmine1,Sue Lucia I1,Nelson Courtney M1,Walker Jessica E1,Glass Michael J1,Arce Richard A1,Fleisher Adam S2,Pontecorvo Michael J2,Atri Alireza13,Montine Thomas J4,Chen Kewei567,Beach Thomas G1

Affiliation:

1. From the Banner Sun Health Research Institute, Sun City, Arizona, USA

2. Avid Radiopharmaceuticals, Philadelphia, Pennsylvania, USA

3. Department of Neurology, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts, USA

4. Department of Pathology, Stanford University, Stanford, California, USA

5. Banner Alzheimer’s Institute, Phoenix, Arizona, USA

6. School of Mathematics and Statistics, Arizona State University, Tempe, Arizona, USA

7. Department of Neurology, College of Medicine Phoenix, University of Arizona, Tucson, Arizona, USA

Abstract

Abstract The spread of neurofibrillary tau pathology in Alzheimer disease (AD) mostly follows a stereotypical pattern of topographical progression but atypical patterns associated with interhemispheric asymmetry have been described. Because histopathological studies that used bilateral sampling are limited, this study aimed to assess interhemispheric tau pathology differences and the presence of topographically atypical cortical spreading patterns. Immunohistochemical staining for detection of tau pathology was performed in 23 regions of interest in 57 autopsy cases comparing bilateral cortical regions and hemispheres. Frequent mild (82% of cases) and occasional moderate (32%) interhemispheric density discrepancies were observed, whereas marked discrepancies were uncommon (7%) and restricted to occipital regions. Left and right hemispheric tau pathology dominance was observed with similar frequencies, except in Braak Stage VI that favored a left dominance. Interhemispheric Braak stage differences were observed in 16% of cases and were more frequent in advanced (IV–VI) versus early (I–III) stages. One atypical lobar topographical pattern in which occipital tau pathology density exceeded frontal lobe scores was identified in 4 cases favoring a left dominant asymmetry. We speculate that asymmetry and atypical topographical progression patterns may be associated with atypical AD clinical presentations and progression characteristics, which should be tested by comprehensive clinicopathological correlations.

Funder

Avid Radiopharmaceuticals

Publisher

Oxford University Press (OUP)

Subject

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

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