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Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment

BACKGROUND/AIMS: Disease-modifying therapy for Alzheimer's disease (AD) has led to a need for biomarkers to identify prodromal AD and very early stage of AD dementia. We aimed to identify the cutoff values of cerebrospinal fluid (CSF) biomarkers for detecting prodromal AD. METHODS: We assessed...

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Autores principales: Park, Jung Eun, Choi, Kyu Yeong, Kim, Byeong C., Choi, Seong-Min, Song, Min-Kyung, Lee, Jang Jae, Kim, Jahae, Song, Ho-Chun, Kim, Hoo-Won, Ha, Jung-Min, Seo, Eun Hyun, Song, Woo Keun, Park, Sung-Gyoo, Lee, Jung Sup, Lee, Kun Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465729/
https://www.ncbi.nlm.nih.gov/pubmed/31011328
http://dx.doi.org/10.1159/000496920
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author Park, Jung Eun
Choi, Kyu Yeong
Kim, Byeong C.
Choi, Seong-Min
Song, Min-Kyung
Lee, Jang Jae
Kim, Jahae
Song, Ho-Chun
Kim, Hoo-Won
Ha, Jung-Min
Seo, Eun Hyun
Song, Woo Keun
Park, Sung-Gyoo
Lee, Jung Sup
Lee, Kun Ho
author_facet Park, Jung Eun
Choi, Kyu Yeong
Kim, Byeong C.
Choi, Seong-Min
Song, Min-Kyung
Lee, Jang Jae
Kim, Jahae
Song, Ho-Chun
Kim, Hoo-Won
Ha, Jung-Min
Seo, Eun Hyun
Song, Woo Keun
Park, Sung-Gyoo
Lee, Jung Sup
Lee, Kun Ho
author_sort Park, Jung Eun
collection PubMed
description BACKGROUND/AIMS: Disease-modifying therapy for Alzheimer's disease (AD) has led to a need for biomarkers to identify prodromal AD and very early stage of AD dementia. We aimed to identify the cutoff values of cerebrospinal fluid (CSF) biomarkers for detecting prodromal AD. METHODS: We assessed 56 patients with amnestic mild cognitive impairment (aMCI) who underwent lumbar puncture. Additionally, 87 healthy elderly individuals and 34 patients with AD dementia served as controls. Positron emission tomography was performed using florbetaben as a probe. We analyzed the concentration of Aβ(1–42), total tau protein (t-Tau), and tau protein phosphorylated at threonine 181 (p-Tau(181)) in CSF with INNOTEST enzyme-linked immunosorbent assay. RESULTS: For the detection of prodromal AD in patients with aMCI, the cutoff values of CSF Aβ(1–42), t-Tau, and p-Tau(181) were 749.5 pg/mL, 225.6 pg/mL, and 43.5 pg/mL, respectively. To discriminate prodromal AD in patients with aMCI, the t-Tau/Aβ(1–42) and ­p-Tau(181)/Aβ(1–42) ratios defined cutoff values at 0.298 and 0.059, respectively. CONCLUSIONS: CSF biomarkers are very useful tools for the differential diagnosis of prodromal AD in aMCI patients. The concentration of CSF biomarkers is well correlated with the stages of the AD spectrum.
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spelling pubmed-64657292019-04-22 Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment Park, Jung Eun Choi, Kyu Yeong Kim, Byeong C. Choi, Seong-Min Song, Min-Kyung Lee, Jang Jae Kim, Jahae Song, Ho-Chun Kim, Hoo-Won Ha, Jung-Min Seo, Eun Hyun Song, Woo Keun Park, Sung-Gyoo Lee, Jung Sup Lee, Kun Ho Dement Geriatr Cogn Dis Extra Original Research Article BACKGROUND/AIMS: Disease-modifying therapy for Alzheimer's disease (AD) has led to a need for biomarkers to identify prodromal AD and very early stage of AD dementia. We aimed to identify the cutoff values of cerebrospinal fluid (CSF) biomarkers for detecting prodromal AD. METHODS: We assessed 56 patients with amnestic mild cognitive impairment (aMCI) who underwent lumbar puncture. Additionally, 87 healthy elderly individuals and 34 patients with AD dementia served as controls. Positron emission tomography was performed using florbetaben as a probe. We analyzed the concentration of Aβ(1–42), total tau protein (t-Tau), and tau protein phosphorylated at threonine 181 (p-Tau(181)) in CSF with INNOTEST enzyme-linked immunosorbent assay. RESULTS: For the detection of prodromal AD in patients with aMCI, the cutoff values of CSF Aβ(1–42), t-Tau, and p-Tau(181) were 749.5 pg/mL, 225.6 pg/mL, and 43.5 pg/mL, respectively. To discriminate prodromal AD in patients with aMCI, the t-Tau/Aβ(1–42) and ­p-Tau(181)/Aβ(1–42) ratios defined cutoff values at 0.298 and 0.059, respectively. CONCLUSIONS: CSF biomarkers are very useful tools for the differential diagnosis of prodromal AD in aMCI patients. The concentration of CSF biomarkers is well correlated with the stages of the AD spectrum. S. Karger AG 2019-03-12 /pmc/articles/PMC6465729/ /pubmed/31011328 http://dx.doi.org/10.1159/000496920 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes as well as any distribution of modified material requires written permission.
spellingShingle Original Research Article
Park, Jung Eun
Choi, Kyu Yeong
Kim, Byeong C.
Choi, Seong-Min
Song, Min-Kyung
Lee, Jang Jae
Kim, Jahae
Song, Ho-Chun
Kim, Hoo-Won
Ha, Jung-Min
Seo, Eun Hyun
Song, Woo Keun
Park, Sung-Gyoo
Lee, Jung Sup
Lee, Kun Ho
Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment
title Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment
title_full Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment
title_fullStr Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment
title_full_unstemmed Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment
title_short Cerebrospinal Fluid Biomarkers for the Diagnosis of Prodromal Alzheimer's Disease in Amnestic Mild Cognitive Impairment
title_sort cerebrospinal fluid biomarkers for the diagnosis of prodromal alzheimer's disease in amnestic mild cognitive impairment
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465729/
https://www.ncbi.nlm.nih.gov/pubmed/31011328
http://dx.doi.org/10.1159/000496920
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