Revisiting the relevance of Hirano bodies in neurodegenerative diseases

Author:

Yoshida Koji123,Forrest Shelley L.1245,Ichimata Shojiro3,Tanaka Hidetomo12,Kon Tomoya126,Tartaglia Maria Carmela78,Tator Charles H.910,Lang Anthony E.28911,Nishida Naoki3ORCID,Kovacs Gabor G.12411ORCID

Affiliation:

1. Department of Laboratory Medicine and Pathobiology and Department of Medicine University of Toronto Toronto Ontario Canada

2. Tanz Centre for Research in Neurodegenerative Disease, Krembil Discovery Tower University of Toronto Toronto Ontario Canada

3. Department of Legal Medicine, Graduate School of Medicine and Pharmaceutical Sciences University of Toyama Toyama Toyama Japan

4. Laboratory Medicine Program & Krembil Brain Institute University Health Network Toronto Ontario Canada

5. Dementia Research Centre, Macquarie Medical School, Faculty of Medicine, Health and Human Sciences Macquarie University Sydney Australia

6. Department of Neurology Hirosaki University Graduate School of Medicine Hirosaki Aomori Japan

7. Institute of Medical Science, Temerty Faculty of Medicine University of Toronto Toronto Ontario Canada

8. Division of Neurology, Department of Medicine University of Toronto Toronto Ontario Canada

9. Krembil Brain Institute Toronto Western Hospital Toronto Ontario Canada

10. Canadian Concussion Centre, Krembil Brain Institute University Health Network Toronto Ontario Canada

11. Edmond J. Safra Program in Parkinson's Disease, Rossy Program for PSP Research and the Morton and Gloria Shulman Movement Disorders Clinic Toronto Western Hospital Toronto ON Canada

Abstract

AbstractAimsHirano bodies (HBs) are eosinophilic pathological structures with two morphological phenotypes commonly found in the hippocampal CA1 region in Alzheimer's disease (AD). This study evaluated the prevalence and distribution of HBs in AD and other neurodegenerative diseases.MethodsThis cross‐sectional study systematically evaluated HBs in a cohort of 193 cases with major neurodegenerative diseases, including AD (n = 91), Lewy body disease (LBD, n = 87), progressive supranuclear palsy (PSP, n = 36), multiple system atrophy (MSA, n = 14) and controls (n = 26). The prevalence, number and morphology of HBs in the stratum lacunosum (HBL) and CA1 pyramidal cell layer were examined. In addition, we investigated the presence of HBs in five additional hippocampal subregions.ResultsThe morphological types of HBs in CA1 were divided into three, including a newly discovered type, and were evaluated separately, with their morphology confirmed in three dimensions: (1) classic rod‐shaped HB (CHB), (2) balloon‐shaped HB (BHB) and the newly described (3) string‐shaped HB (SHB). The prevalence of each HB type differed between disease groups: Compared with controls, for CHB in AD, AD + LBD, PSP and corticobasal degeneration, for BHB in AD + LBD and PSP, and SHB in AD + LBD and PSP were significantly increased. Regression analysis showed that CHBs were independently associated with higher Braak NFT stage, BHBs with LBD and TDP‐43 pathology, SHBs with higher Braak NFT stage, PSP and argyrophilic grain disease and HBLs with MSA.ConclusionsThis study demonstrates that HBs are associated with diverse neurodegenerative diseases and shows that morphological types appear distinctively in various conditions.

Funder

Edmond J. Safra Philanthropic Foundation

Canada Foundation for Innovation

Publisher

Wiley

Reference75 articles.

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