Olfactory Dysfunction Is Associated with Cerebral Amyloid Deposition and Cognitive Function in the Trajectory of Alzheimer’s Disease

Bibliographic Details
Title: Olfactory Dysfunction Is Associated with Cerebral Amyloid Deposition and Cognitive Function in the Trajectory of Alzheimer’s Disease
Authors: Sheng-Min Wang, Dong Woo Kang, Yoo Hyun Um, Sunghwan Kim, Chang Uk Lee, Hyun Kook Lim
Source: Biomolecules, Vol 13, Iss 9, p 1336 (2023)
Publisher Information: MDPI AG, 2023.
Publication Year: 2023
Collection: LCC:Microbiology
Subject Terms: olfaction, Alzheimer’s disease, mild cognitive impairment, beta-amyloid, association, Microbiology, QR1-502
More Details: Olfactory dysfunction is consistently observed in individuals with Alzheimer’s disease (AD), but its association with beta-amyloid (Aβ) deposition remains unclear. This study aimed to investigate the relationship among olfactory function, cerebral Aβ deposition, and neuropsychological profiles in individuals with no cognitive impairment (NCI), mild cognitive impairment (MCI), and AD dementia. A total of 164 participants were included, and olfactory function was assessed using the brief smell identification test (B-SIT). Cerebral Aβ deposition was measured using [18F]-flutemetamol PET imaging (A-PET). The results show a significant group difference in olfactory function, with the highest impairment observed in the Aβ-positive MCI and AD dementia groups, and the impairment was the lowest in Aβ-negative NCI. Olfactory dysfunction was positively associated with cognitive impairments across multiple domains. Furthermore, individuals with Aβ deposition had lower olfactory function compared to those without Aβ, even within the same neuropsychological stage. The association between olfactory dysfunction and Aβ deposition was observed globally and in specific cortical regions. These findings suggest that olfactory dysfunction is associated with both cognitive function and cerebral Aβ pathology in the trajectory of AD. Olfactory deficits may serve as an additional marker for disease progression and contribute to understanding the underlying mechanisms of AD.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 13091336
2218-273X
Relation: https://www.mdpi.com/2218-273X/13/9/1336; https://doaj.org/toc/2218-273X
DOI: 10.3390/biom13091336
Access URL: https://doaj.org/article/65c137ffda7541c69671cd99676c3a8c
Accession Number: edsdoj.65c137ffda7541c69671cd99676c3a8c
Database: Directory of Open Access Journals
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More Details
ISSN:13091336
2218273X
DOI:10.3390/biom13091336
Published in:Biomolecules
Language:English