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Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens

Studies in the field of Alzheimer’s disease (AD) have shown the emergence of biomarkers in biologic fluids that hold great promise for the diagnosis of the disease. A diagnosis of AD at a presymptomatic or early stage may be the key for a successful treatment, with clinical trials currently investig...

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Autores principales: Paraskevaidi, Maria, Allsop, David, Karim, Salman, Martin, Francis L., Crean, StJohn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356561/
https://www.ncbi.nlm.nih.gov/pubmed/32492907
http://dx.doi.org/10.3390/jcm9061673
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author Paraskevaidi, Maria
Allsop, David
Karim, Salman
Martin, Francis L.
Crean, StJohn
author_facet Paraskevaidi, Maria
Allsop, David
Karim, Salman
Martin, Francis L.
Crean, StJohn
author_sort Paraskevaidi, Maria
collection PubMed
description Studies in the field of Alzheimer’s disease (AD) have shown the emergence of biomarkers in biologic fluids that hold great promise for the diagnosis of the disease. A diagnosis of AD at a presymptomatic or early stage may be the key for a successful treatment, with clinical trials currently investigating this. It is anticipated that preventative and therapeutic strategies may be stage-dependent, which means that they have a better chance of success at a very early stage—before critical neurons are lost. Several studies have been investigating the use of cerebrospinal fluid (CSF) and blood as clinical samples for the detection of AD with a number of established core markers, such as amyloid beta (Aβ), total tau (T-tau) and phosphorylated tau (P-tau), being at the center of clinical research interest. The use of oral samples—including saliva and buccal mucosal cells—falls under one of the least-investigated areas in AD diagnosis. Such samples have great potential to provide a completely non-invasive alternative to current CSF and blood sampling procedures. The present work is a thorough review of the results and analytical approaches, including proteomics, metabolomics, spectroscopy and microbiome analyses that have been used for the study and detection of AD using salivary samples and buccal cells. With a few exceptions, most of the studies utilizing oral samples were performed in small cohorts, which in combination with the existence of contradictory results render it difficult to come to a definitive conclusion on the value of oral markers. Proteins such as Aβ, T-tau and P-tau, as well as small metabolites, were detected in saliva and have shown some potential as future AD diagnostics. Future large-cohort studies and standardization of sample preparation and (pre-)analytical factors are necessary to determine the use of these non-invasive samples as a diagnostic tool for AD.
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spelling pubmed-73565612020-07-30 Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens Paraskevaidi, Maria Allsop, David Karim, Salman Martin, Francis L. Crean, StJohn J Clin Med Review Studies in the field of Alzheimer’s disease (AD) have shown the emergence of biomarkers in biologic fluids that hold great promise for the diagnosis of the disease. A diagnosis of AD at a presymptomatic or early stage may be the key for a successful treatment, with clinical trials currently investigating this. It is anticipated that preventative and therapeutic strategies may be stage-dependent, which means that they have a better chance of success at a very early stage—before critical neurons are lost. Several studies have been investigating the use of cerebrospinal fluid (CSF) and blood as clinical samples for the detection of AD with a number of established core markers, such as amyloid beta (Aβ), total tau (T-tau) and phosphorylated tau (P-tau), being at the center of clinical research interest. The use of oral samples—including saliva and buccal mucosal cells—falls under one of the least-investigated areas in AD diagnosis. Such samples have great potential to provide a completely non-invasive alternative to current CSF and blood sampling procedures. The present work is a thorough review of the results and analytical approaches, including proteomics, metabolomics, spectroscopy and microbiome analyses that have been used for the study and detection of AD using salivary samples and buccal cells. With a few exceptions, most of the studies utilizing oral samples were performed in small cohorts, which in combination with the existence of contradictory results render it difficult to come to a definitive conclusion on the value of oral markers. Proteins such as Aβ, T-tau and P-tau, as well as small metabolites, were detected in saliva and have shown some potential as future AD diagnostics. Future large-cohort studies and standardization of sample preparation and (pre-)analytical factors are necessary to determine the use of these non-invasive samples as a diagnostic tool for AD. MDPI 2020-06-01 /pmc/articles/PMC7356561/ /pubmed/32492907 http://dx.doi.org/10.3390/jcm9061673 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Paraskevaidi, Maria
Allsop, David
Karim, Salman
Martin, Francis L.
Crean, StJohn
Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens
title Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens
title_full Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens
title_fullStr Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens
title_full_unstemmed Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens
title_short Diagnostic Biomarkers for Alzheimer’s Disease Using Non-Invasive Specimens
title_sort diagnostic biomarkers for alzheimer’s disease using non-invasive specimens
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356561/
https://www.ncbi.nlm.nih.gov/pubmed/32492907
http://dx.doi.org/10.3390/jcm9061673
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