Investigation of amyloid‐beta 42 levels in human nasal discharge fluid from healthy and Alzheimer’s discovers diagnostic values

Abstract Background Alzheimer’s disease (AD) therapy requires timely and accurate diagnosis for prompt drug intervention, emphasizing the need for a more accessible biomarker screening test. Previous studies identified higher expression of oligomeric Aβ in AD patients, however, the quantitative measurements of nasal Aβ42 levels of the full AD continuum remain unknown. Method We collected nasal discharge samples from 161 subjects who underwent neuropsychological battery tests and amyloid‐PET and nasal Aβ42 levels were measured via enzyme‐linked immunosorbent assay (ELISA). Result Our results revealed that the second‐highest quartile (Q3) group of nasal Aβ42 had the majority of patients with AD diagnosis, and those in the Q3 group exhibited the most impaired cognitive function with a strong significance. Nasal Aβ42 levels were also associated with brain amyloid PET results and increased risk of developing AD. Conclusion Our findings suggest that nasal Aβ42 is a promising biomarker for AD diagnosis and risk assessment.

Authors

Institutions

Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.094935
Primary Topic
Neurological Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Investigation of amyloid‐beta 42 levels in human nasal discharge fluid from healthy and Alzheimer’s discovers diagnostic values

Gowoon Son, Hyun Kook Lim, Cheil Moon, Da Hae Jung et al.
Alzheimer s & Dementia
Neurological Disease Mechanisms and Treatments
article

Investigation of amyloid‐beta 42 levels in human nasal discharge fluid from healthy and Alzheimer’s discovers diagnostic values

Gowoon Son, Hyun Kook Lim, Cheil Moon, Da Hae Jung, Sheng‐Min Wang
article en

Abstract

Abstract Background Alzheimer’s disease (AD) therapy requires timely and accurate diagnosis for prompt drug intervention, emphasizing the need for a more accessible biomarker screening test. Previous studies identified higher expression of oligomeric Aβ in AD patients, however, the quantitative measurements of nasal Aβ42 levels of the full AD continuum remain unknown. Method We collected nasal discharge samples from 161 subjects who underwent neuropsychological battery tests and amyloid‐PET and nasal Aβ42 levels were measured via enzyme‐linked immunosorbent assay (ELISA). Result Our results revealed that the second‐highest quartile (Q3) group of nasal Aβ42 had the majority of patients with AD diagnosis, and those in the Q3 group exhibited the most impaired cognitive function with a strong significance. Nasal Aβ42 levels were also associated with brain amyloid PET results and increased risk of developing AD. Conclusion Our findings suggest that nasal Aβ42 is a promising biomarker for AD diagnosis and risk assessment.

Alzheimer s & DementiaVol. 20(S8)
University of California, San Francisco (US), Daegu Gyeongbuk Institute of Science and Technology (KR), Maastricht University (NL), University Memory and Aging Center (US), The Catholic University of Korea Yeouido St. Mary's Hospital (KR), Catholic University of Korea (KR)
Openalex Percentile: Top 71%
Neurological Disease Mechanisms and Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.