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Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study
BACKGROUND: There are only few population-based studies that have systemically investigated the prevalence of hippocampal sclerosis (HS) in the very old. The frequency of unilateral versus bilateral HS has been rarely studied. OBJECTIVE: We investigated the prevalence and laterality of HS and its as...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900558/ https://www.ncbi.nlm.nih.gov/pubmed/29614661 http://dx.doi.org/10.3233/JAD-171068 |
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author | Kero, Mia Raunio, Anna Polvikoski, Tuomo Tienari, Pentti J. Paetau, Anders Myllykangas, Liisa |
author_facet | Kero, Mia Raunio, Anna Polvikoski, Tuomo Tienari, Pentti J. Paetau, Anders Myllykangas, Liisa |
author_sort | Kero, Mia |
collection | PubMed |
description | BACKGROUND: There are only few population-based studies that have systemically investigated the prevalence of hippocampal sclerosis (HS) in the very old. The frequency of unilateral versus bilateral HS has been rarely studied. OBJECTIVE: We investigated the prevalence and laterality of HS and its association with other neurodegenerative and vascular pathologies in a population-based sample of very elderly. Furthermore, the concomitant presence of immunoreactivity for TDP-43, p62, and HPtau was studied. METHODS: The population-based Vantaa 85+ study includes all inhabitants of the city of Vantaa, who were >85 years in 1991 (n = 601). Neuropathological assessment was possible in 302 subjects. Severity of neuronal loss of CA sectors and subiculum was determined bilaterally by HE- staining. Immunohistochemistry performed using antibodies for TDP-43, p62, and HPtau. RESULTS: Neuronal loss and pathological changes in the hippocampus sector CA1 and subiculum were observed in 47 of the 302 individuals (16%), and 51% of these changes were bilateral. HS without comorbid neurodegenerative pathology was found in 1/47 subjects with HS (2%). Dementia (p < 0.001) and TDP-43 immunopositivity of the granular cell layer of the dentate fascia (p < 0.001) were strongly associated with HS. The CERAD score, immunopositivity for HPtau and p62 in the granular cell layer of the fascia dentate were also associated. CONCLUSION: HS is prevalent (16%) in the oldest old population, but HS without any comorbid neurodegenerative pathology is rare. The high frequency of unilateral HS (49%) implied that bilateral sampling of hippocampi should be routine practice in neuropathological examination. |
format | Online Article Text |
id | pubmed-5900558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59005582018-04-19 Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study Kero, Mia Raunio, Anna Polvikoski, Tuomo Tienari, Pentti J. Paetau, Anders Myllykangas, Liisa J Alzheimers Dis Research Article BACKGROUND: There are only few population-based studies that have systemically investigated the prevalence of hippocampal sclerosis (HS) in the very old. The frequency of unilateral versus bilateral HS has been rarely studied. OBJECTIVE: We investigated the prevalence and laterality of HS and its association with other neurodegenerative and vascular pathologies in a population-based sample of very elderly. Furthermore, the concomitant presence of immunoreactivity for TDP-43, p62, and HPtau was studied. METHODS: The population-based Vantaa 85+ study includes all inhabitants of the city of Vantaa, who were >85 years in 1991 (n = 601). Neuropathological assessment was possible in 302 subjects. Severity of neuronal loss of CA sectors and subiculum was determined bilaterally by HE- staining. Immunohistochemistry performed using antibodies for TDP-43, p62, and HPtau. RESULTS: Neuronal loss and pathological changes in the hippocampus sector CA1 and subiculum were observed in 47 of the 302 individuals (16%), and 51% of these changes were bilateral. HS without comorbid neurodegenerative pathology was found in 1/47 subjects with HS (2%). Dementia (p < 0.001) and TDP-43 immunopositivity of the granular cell layer of the dentate fascia (p < 0.001) were strongly associated with HS. The CERAD score, immunopositivity for HPtau and p62 in the granular cell layer of the fascia dentate were also associated. CONCLUSION: HS is prevalent (16%) in the oldest old population, but HS without any comorbid neurodegenerative pathology is rare. The high frequency of unilateral HS (49%) implied that bilateral sampling of hippocampi should be routine practice in neuropathological examination. IOS Press 2018-04-10 /pmc/articles/PMC5900558/ /pubmed/29614661 http://dx.doi.org/10.3233/JAD-171068 Text en © 2018 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kero, Mia Raunio, Anna Polvikoski, Tuomo Tienari, Pentti J. Paetau, Anders Myllykangas, Liisa Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study |
title | Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study |
title_full | Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study |
title_fullStr | Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study |
title_full_unstemmed | Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study |
title_short | Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study |
title_sort | hippocampal sclerosis in the oldest old: a finnish population-based study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900558/ https://www.ncbi.nlm.nih.gov/pubmed/29614661 http://dx.doi.org/10.3233/JAD-171068 |
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