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Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease

Odor identification ability may serve as an important diagnostic biomarker in Alzheimer’s disease (AD). The aim of the study is to investigate the contribution of A/T/N neuroimaging biomarkers to impaired odor identification ability in the Alzheimer’s disease spectrum. In 127 participants, we compar...

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Autores principales: Baek, Min Seok, Cho, Hanna, Lee, Hye Sun, Lee, Jae Hoon, Ryu, Young Hoon, Lyoo, Chul Hyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360607/
https://www.ncbi.nlm.nih.gov/pubmed/32665636
http://dx.doi.org/10.1038/s41598-020-68504-2
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author Baek, Min Seok
Cho, Hanna
Lee, Hye Sun
Lee, Jae Hoon
Ryu, Young Hoon
Lyoo, Chul Hyoung
author_facet Baek, Min Seok
Cho, Hanna
Lee, Hye Sun
Lee, Jae Hoon
Ryu, Young Hoon
Lyoo, Chul Hyoung
author_sort Baek, Min Seok
collection PubMed
description Odor identification ability may serve as an important diagnostic biomarker in Alzheimer’s disease (AD). The aim of the study is to investigate the contribution of A/T/N neuroimaging biomarkers to impaired odor identification ability in the Alzheimer’s disease spectrum. In 127 participants, we compared A/T/N neuroimaging biomarkers between normosmia and hyposmia groups, and performed correlation analysis between the biomarkers and Cross-Cultural Smell Identification Test (CCSIT) scores. Additionally, path analysis for odor identification ability was performed using cognitive function as a mediator. In between-group comparison, individuals with hyposmia showed higher frequency of amyloid-β (Aβ) positivity, and lower neuropsychological test performance than those with normosmia. After correction for covariates including total cognition scores, there was no difference in the Aβ or tau burden between the normosmia and hyposmia groups, and no correlation between CCSIT scores and Aβ or tau burden. Meanwhile, cortical volumes in the lateral and medial temporal cortices were smaller in the hyposmia group and decreased with the worsening of CCSIT scores. Path analysis showed that only neurodegeneration had a direct effect on odor identification, while Aβ and tau burden contributed to odor identification with the mediation of cognition. In the Alzheimer’s disease spectrum, impaired odor identification ability may be attributable to neurodegeneration rather than the direct effect of Aβ or tau burden.
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spelling pubmed-73606072020-07-16 Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease Baek, Min Seok Cho, Hanna Lee, Hye Sun Lee, Jae Hoon Ryu, Young Hoon Lyoo, Chul Hyoung Sci Rep Article Odor identification ability may serve as an important diagnostic biomarker in Alzheimer’s disease (AD). The aim of the study is to investigate the contribution of A/T/N neuroimaging biomarkers to impaired odor identification ability in the Alzheimer’s disease spectrum. In 127 participants, we compared A/T/N neuroimaging biomarkers between normosmia and hyposmia groups, and performed correlation analysis between the biomarkers and Cross-Cultural Smell Identification Test (CCSIT) scores. Additionally, path analysis for odor identification ability was performed using cognitive function as a mediator. In between-group comparison, individuals with hyposmia showed higher frequency of amyloid-β (Aβ) positivity, and lower neuropsychological test performance than those with normosmia. After correction for covariates including total cognition scores, there was no difference in the Aβ or tau burden between the normosmia and hyposmia groups, and no correlation between CCSIT scores and Aβ or tau burden. Meanwhile, cortical volumes in the lateral and medial temporal cortices were smaller in the hyposmia group and decreased with the worsening of CCSIT scores. Path analysis showed that only neurodegeneration had a direct effect on odor identification, while Aβ and tau burden contributed to odor identification with the mediation of cognition. In the Alzheimer’s disease spectrum, impaired odor identification ability may be attributable to neurodegeneration rather than the direct effect of Aβ or tau burden. Nature Publishing Group UK 2020-07-14 /pmc/articles/PMC7360607/ /pubmed/32665636 http://dx.doi.org/10.1038/s41598-020-68504-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Baek, Min Seok
Cho, Hanna
Lee, Hye Sun
Lee, Jae Hoon
Ryu, Young Hoon
Lyoo, Chul Hyoung
Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease
title Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease
title_full Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease
title_fullStr Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease
title_full_unstemmed Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease
title_short Effect of A/T/N imaging biomarkers on impaired odor identification in Alzheimer's disease
title_sort effect of a/t/n imaging biomarkers on impaired odor identification in alzheimer's disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360607/
https://www.ncbi.nlm.nih.gov/pubmed/32665636
http://dx.doi.org/10.1038/s41598-020-68504-2
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