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Effect of olfactory bulb pathology on olfactory function in normal aging

Decline of olfactory function is frequently observed in aging and is an early symptom of neurodegenerative diseases. As the olfactory bulb (OB) is one of the first regions involved by pathology and may represent an early disease stage, we specifically aimed to evaluate the contribution of OB patholo...

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Autores principales: Tremblay, Cécilia, Serrano, Geidy E., Intorcia, Anthony J., Sue, Lucia I., Wilson, Jeffrey R., Adler, Charles H., Shill, Holly A., Driver‐Dunckley, Erika, Mehta, Shyamal H., Beach, Thomas G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424999/
https://www.ncbi.nlm.nih.gov/pubmed/35485279
http://dx.doi.org/10.1111/bpa.13075
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author Tremblay, Cécilia
Serrano, Geidy E.
Intorcia, Anthony J.
Sue, Lucia I.
Wilson, Jeffrey R.
Adler, Charles H.
Shill, Holly A.
Driver‐Dunckley, Erika
Mehta, Shyamal H.
Beach, Thomas G.
author_facet Tremblay, Cécilia
Serrano, Geidy E.
Intorcia, Anthony J.
Sue, Lucia I.
Wilson, Jeffrey R.
Adler, Charles H.
Shill, Holly A.
Driver‐Dunckley, Erika
Mehta, Shyamal H.
Beach, Thomas G.
author_sort Tremblay, Cécilia
collection PubMed
description Decline of olfactory function is frequently observed in aging and is an early symptom of neurodegenerative diseases. As the olfactory bulb (OB) is one of the first regions involved by pathology and may represent an early disease stage, we specifically aimed to evaluate the contribution of OB pathology to olfactory decline in cognitively normal aged individuals without parkinsonism or dementia. This clinicopathological study correlates OB tau, amyloid β (Aβ) and α‐synuclein (αSyn) pathology densities and whole brain pathology load to olfactory identification function as measured with the University of Pennsylvania Smell Identification Test (UPSIT) and clinical data measured proximate to death in a large autopsy study including 138 cases considered non‐demented controls during life. Tau pathology was frequently observed in the OB (95% of cases), while both Aβ (27% of cases) and αSyn (20% of cases) OB pathologies were less commonly observed. A weak correlation was only observed between OB tau and olfactory performance, but when controlled for age, neither OB tau, Aβ or αSyn significantly predict olfactory performance. Moreover, whole brain tau and αSyn pathology loads predicted olfactory performance; however, only αSyn pathology loads survived age correction. In conclusion, OB tau pathology is frequently observed in normally aging individuals and increases with age but does not appear to independently contribute to age‐related olfactory impairment suggesting that further involvement of the brain seems necessary to contribute to age‐related olfactory decline.
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spelling pubmed-94249992022-08-31 Effect of olfactory bulb pathology on olfactory function in normal aging Tremblay, Cécilia Serrano, Geidy E. Intorcia, Anthony J. Sue, Lucia I. Wilson, Jeffrey R. Adler, Charles H. Shill, Holly A. Driver‐Dunckley, Erika Mehta, Shyamal H. Beach, Thomas G. Brain Pathol Letters to the Editor Decline of olfactory function is frequently observed in aging and is an early symptom of neurodegenerative diseases. As the olfactory bulb (OB) is one of the first regions involved by pathology and may represent an early disease stage, we specifically aimed to evaluate the contribution of OB pathology to olfactory decline in cognitively normal aged individuals without parkinsonism or dementia. This clinicopathological study correlates OB tau, amyloid β (Aβ) and α‐synuclein (αSyn) pathology densities and whole brain pathology load to olfactory identification function as measured with the University of Pennsylvania Smell Identification Test (UPSIT) and clinical data measured proximate to death in a large autopsy study including 138 cases considered non‐demented controls during life. Tau pathology was frequently observed in the OB (95% of cases), while both Aβ (27% of cases) and αSyn (20% of cases) OB pathologies were less commonly observed. A weak correlation was only observed between OB tau and olfactory performance, but when controlled for age, neither OB tau, Aβ or αSyn significantly predict olfactory performance. Moreover, whole brain tau and αSyn pathology loads predicted olfactory performance; however, only αSyn pathology loads survived age correction. In conclusion, OB tau pathology is frequently observed in normally aging individuals and increases with age but does not appear to independently contribute to age‐related olfactory impairment suggesting that further involvement of the brain seems necessary to contribute to age‐related olfactory decline. John Wiley and Sons Inc. 2022-04-29 /pmc/articles/PMC9424999/ /pubmed/35485279 http://dx.doi.org/10.1111/bpa.13075 Text en © 2022 The Authors. Brain Pathology published by John Wiley & Sons Ltd on behalf of International Society of Neuropathology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters to the Editor
Tremblay, Cécilia
Serrano, Geidy E.
Intorcia, Anthony J.
Sue, Lucia I.
Wilson, Jeffrey R.
Adler, Charles H.
Shill, Holly A.
Driver‐Dunckley, Erika
Mehta, Shyamal H.
Beach, Thomas G.
Effect of olfactory bulb pathology on olfactory function in normal aging
title Effect of olfactory bulb pathology on olfactory function in normal aging
title_full Effect of olfactory bulb pathology on olfactory function in normal aging
title_fullStr Effect of olfactory bulb pathology on olfactory function in normal aging
title_full_unstemmed Effect of olfactory bulb pathology on olfactory function in normal aging
title_short Effect of olfactory bulb pathology on olfactory function in normal aging
title_sort effect of olfactory bulb pathology on olfactory function in normal aging
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424999/
https://www.ncbi.nlm.nih.gov/pubmed/35485279
http://dx.doi.org/10.1111/bpa.13075
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