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Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain

OBJECTIVE: We aimed to examine whether impaired olfaction is associated with cognitive decline and indicators of neurodegeneration in the brain of dementia-free older adults. METHODS: Within the Rush Memory and Aging Project, 380 dementia-free participants (mean age = 78 years) were followed for up...

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Autores principales: Dintica, Christina S., Marseglia, Anna, Rizzuto, Debora, Wang, Rui, Seubert, Janina, Arfanakis, Konstantinos, Bennett, David A., Xu, Weili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382360/
https://www.ncbi.nlm.nih.gov/pubmed/30651382
http://dx.doi.org/10.1212/WNL.0000000000006919
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author Dintica, Christina S.
Marseglia, Anna
Rizzuto, Debora
Wang, Rui
Seubert, Janina
Arfanakis, Konstantinos
Bennett, David A.
Xu, Weili
author_facet Dintica, Christina S.
Marseglia, Anna
Rizzuto, Debora
Wang, Rui
Seubert, Janina
Arfanakis, Konstantinos
Bennett, David A.
Xu, Weili
author_sort Dintica, Christina S.
collection PubMed
description OBJECTIVE: We aimed to examine whether impaired olfaction is associated with cognitive decline and indicators of neurodegeneration in the brain of dementia-free older adults. METHODS: Within the Rush Memory and Aging Project, 380 dementia-free participants (mean age = 78 years) were followed for up to 15 years, and underwent MRI scans. Olfactory function was assessed using the Brief Smell Identification Test (B-SIT) at baseline, and categorized as anosmia (B-SIT <6), hyposmia (B-SIT 6–10 in men and 6–10.25 in women), and normal (B-SIT 10.25–12 in men and 10.5–12 in women). Cognitive function was annually assessed with a battery of 21 tests, from which composite scores were derived. Structural total and regional brain volumes were estimated. Data were analyzed using linear regression and mixed-effects models. RESULTS: At study entry, 138 (36.3%) had normal olfactory function, 213 (56.1%) had hyposmia, and 29 (7.6%) had anosmia. In multiadjusted mixed-effects models, hyposmia (β = −0.03, 95% confidence interval [CI] −0.05 to −0.02) and anosmia (β = −0.13, 95% CI −0.16 to −0.09) were associated with faster rate of cognitive decline compared to normal olfaction. On MRI, impaired olfaction (hyposmia or anosmia) was related to smaller volumes of the hippocampus (β = −0.19, 95% CI −0.33 to −0.05), and in the entorhinal (β = −0.16, 95% CI −0.24 to −0.08), fusiform (β = −0.45, 95% CI −0.78 to −0.14), and middle temporal (β = −0.38, 95% CI −0.72 to −0.01) cortices. CONCLUSION: Impaired olfaction predicts faster cognitive decline and might indicate neurodegeneration in the brain among dementia-free older adults.
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spelling pubmed-63823602019-04-11 Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain Dintica, Christina S. Marseglia, Anna Rizzuto, Debora Wang, Rui Seubert, Janina Arfanakis, Konstantinos Bennett, David A. Xu, Weili Neurology Article OBJECTIVE: We aimed to examine whether impaired olfaction is associated with cognitive decline and indicators of neurodegeneration in the brain of dementia-free older adults. METHODS: Within the Rush Memory and Aging Project, 380 dementia-free participants (mean age = 78 years) were followed for up to 15 years, and underwent MRI scans. Olfactory function was assessed using the Brief Smell Identification Test (B-SIT) at baseline, and categorized as anosmia (B-SIT <6), hyposmia (B-SIT 6–10 in men and 6–10.25 in women), and normal (B-SIT 10.25–12 in men and 10.5–12 in women). Cognitive function was annually assessed with a battery of 21 tests, from which composite scores were derived. Structural total and regional brain volumes were estimated. Data were analyzed using linear regression and mixed-effects models. RESULTS: At study entry, 138 (36.3%) had normal olfactory function, 213 (56.1%) had hyposmia, and 29 (7.6%) had anosmia. In multiadjusted mixed-effects models, hyposmia (β = −0.03, 95% confidence interval [CI] −0.05 to −0.02) and anosmia (β = −0.13, 95% CI −0.16 to −0.09) were associated with faster rate of cognitive decline compared to normal olfaction. On MRI, impaired olfaction (hyposmia or anosmia) was related to smaller volumes of the hippocampus (β = −0.19, 95% CI −0.33 to −0.05), and in the entorhinal (β = −0.16, 95% CI −0.24 to −0.08), fusiform (β = −0.45, 95% CI −0.78 to −0.14), and middle temporal (β = −0.38, 95% CI −0.72 to −0.01) cortices. CONCLUSION: Impaired olfaction predicts faster cognitive decline and might indicate neurodegeneration in the brain among dementia-free older adults. Lippincott Williams & Wilkins 2019-02-12 /pmc/articles/PMC6382360/ /pubmed/30651382 http://dx.doi.org/10.1212/WNL.0000000000006919 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Dintica, Christina S.
Marseglia, Anna
Rizzuto, Debora
Wang, Rui
Seubert, Janina
Arfanakis, Konstantinos
Bennett, David A.
Xu, Weili
Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain
title Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain
title_full Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain
title_fullStr Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain
title_full_unstemmed Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain
title_short Impaired olfaction is associated with cognitive decline and neurodegeneration in the brain
title_sort impaired olfaction is associated with cognitive decline and neurodegeneration in the brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382360/
https://www.ncbi.nlm.nih.gov/pubmed/30651382
http://dx.doi.org/10.1212/WNL.0000000000006919
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