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Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment

BACKGROUND AND PURPOSE: The cerebrospinal fluid (CSF) biomarkers play an important supportive role as diagnostic and predictive indicators of Alzheimer's disease (AD). About 30% of controls in old age show abnormal values of CSF biomarkers and display a higher risk for AD compared with those sh...

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Autores principales: Kim, Jong Hun, Lim, Hyunsun, Lee, Jee-un, Cho, Jeong Hee, Kim, Gyu Sik, Choi, Seong Hye, Lee, Jun Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dementia Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428002/
https://www.ncbi.nlm.nih.gov/pubmed/30906382
http://dx.doi.org/10.12779/dnd.2017.16.4.114
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author Kim, Jong Hun
Lim, Hyunsun
Lee, Jee-un
Cho, Jeong Hee
Kim, Gyu Sik
Choi, Seong Hye
Lee, Jun Hong
author_facet Kim, Jong Hun
Lim, Hyunsun
Lee, Jee-un
Cho, Jeong Hee
Kim, Gyu Sik
Choi, Seong Hye
Lee, Jun Hong
author_sort Kim, Jong Hun
collection PubMed
description BACKGROUND AND PURPOSE: The cerebrospinal fluid (CSF) biomarkers play an important supportive role as diagnostic and predictive indicators of Alzheimer's disease (AD). About 30% of controls in old age show abnormal values of CSF biomarkers and display a higher risk for AD compared with those showing normal values. The cut-off values are determined by their diagnostic accuracy. However, the current cut-off values may be less accurate, because controls include high-risk groups of AD. We sought to develop models of patients with AD, who are homogenous for CSF biomarkers. METHODS: We included participants who had CSF biomarker data in the Alzheimer's Disease Neuroimaging Initiative database. We investigated the factors related to CSF biomarkers in patients with AD using linear mixed models. Using the factors, we developed models corresponding to CSF biomarkers to classify patients with mild cognitive impairment (MCI) into high risk and low risk and analyzed the conversion from MCI to AD using the Cox proportional hazards model. RESULTS: APOE ε4 status and age were significantly related to CSF Aβ(1-42). CSF t-tau, APOE ε2 status and sex were significant factors. The CSF p-tau(181) was associated with age and frequency of diagnosis. Accordingly, we modeled the three CSF biomarkers of AD. In MCI without APOE ε4, our models were better predictors of conversion. CONCLUSIONS: We can interpret CSF biomarkers based on the models derived from the data obtained from patients with AD.
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spelling pubmed-64280022019-03-22 Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment Kim, Jong Hun Lim, Hyunsun Lee, Jee-un Cho, Jeong Hee Kim, Gyu Sik Choi, Seong Hye Lee, Jun Hong Dement Neurocogn Disord Original Article BACKGROUND AND PURPOSE: The cerebrospinal fluid (CSF) biomarkers play an important supportive role as diagnostic and predictive indicators of Alzheimer's disease (AD). About 30% of controls in old age show abnormal values of CSF biomarkers and display a higher risk for AD compared with those showing normal values. The cut-off values are determined by their diagnostic accuracy. However, the current cut-off values may be less accurate, because controls include high-risk groups of AD. We sought to develop models of patients with AD, who are homogenous for CSF biomarkers. METHODS: We included participants who had CSF biomarker data in the Alzheimer's Disease Neuroimaging Initiative database. We investigated the factors related to CSF biomarkers in patients with AD using linear mixed models. Using the factors, we developed models corresponding to CSF biomarkers to classify patients with mild cognitive impairment (MCI) into high risk and low risk and analyzed the conversion from MCI to AD using the Cox proportional hazards model. RESULTS: APOE ε4 status and age were significantly related to CSF Aβ(1-42). CSF t-tau, APOE ε2 status and sex were significant factors. The CSF p-tau(181) was associated with age and frequency of diagnosis. Accordingly, we modeled the three CSF biomarkers of AD. In MCI without APOE ε4, our models were better predictors of conversion. CONCLUSIONS: We can interpret CSF biomarkers based on the models derived from the data obtained from patients with AD. Korean Dementia Association 2017-12 2017-12-31 /pmc/articles/PMC6428002/ /pubmed/30906382 http://dx.doi.org/10.12779/dnd.2017.16.4.114 Text en © 2017 Korean Dementia Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Jong Hun
Lim, Hyunsun
Lee, Jee-un
Cho, Jeong Hee
Kim, Gyu Sik
Choi, Seong Hye
Lee, Jun Hong
Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment
title Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment
title_full Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment
title_fullStr Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment
title_full_unstemmed Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment
title_short Cerebrospinal Biomarker Cut-off Methods Defined Only by Alzheimer's Disease Predict More Precisely Conversions of Mild Cognitive Impairment
title_sort cerebrospinal biomarker cut-off methods defined only by alzheimer's disease predict more precisely conversions of mild cognitive impairment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6428002/
https://www.ncbi.nlm.nih.gov/pubmed/30906382
http://dx.doi.org/10.12779/dnd.2017.16.4.114
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