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Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review

BACKGROUND: The histopathological changes of Alzheimer's disease (AD) are detectable decades prior to its clinical expression. However, there is a need for an early, inexpensive, noninvasive diagnostic biomarker to detect specific Alzheimer pathology. Recently developed neuroimaging biomarkers...

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Autores principales: Gleerup, Helena Sophia, Hasselbalch, Steen Gregers, Simonsen, Anja Hviid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525835/
https://www.ncbi.nlm.nih.gov/pubmed/31191751
http://dx.doi.org/10.1155/2019/4761054
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author Gleerup, Helena Sophia
Hasselbalch, Steen Gregers
Simonsen, Anja Hviid
author_facet Gleerup, Helena Sophia
Hasselbalch, Steen Gregers
Simonsen, Anja Hviid
author_sort Gleerup, Helena Sophia
collection PubMed
description BACKGROUND: The histopathological changes of Alzheimer's disease (AD) are detectable decades prior to its clinical expression. However, there is a need for an early, inexpensive, noninvasive diagnostic biomarker to detect specific Alzheimer pathology. Recently developed neuroimaging biomarkers show promising results, but these methods are expensive and cause radiation. Furthermore, the analysis of cerebrospinal fluid (CSF) biomarkers requires an invasive lumbar puncture. Saliva is an easily obtained body fluid, and a stable saliva biomarker would therefore be a promising candidate for a future method for diagnosing AD. The purpose of this systematic review was to investigate studies of biomarkers in saliva samples for the diagnosis of AD. METHODS: The included articles were identified through a literature search in PubMed and Google Scholar for all articles until November 1(st), 2018, and furthermore, all reference lists of included articles were reviewed by hand. We included articles written in English investigating saliva from patients with AD and a control group. RESULTS: A total of 65 studies were identified, whereof 16 studies met the inclusion criteria and were included in the systematic review. A plethora of different biomarkers were investigated, and ten out of the sixteen studies showed a statistical significance in biomarkers between patients with AD and healthy, elderly controls, among these biomarkers for specific AD pathology (amyloid beta 1-42 (Aβ42) and tau). CONCLUSION: Aβ42 and tau seem to be worthy candidates for future salivary biomarkers for AD, but other biomarkers such as lactoferrin and selected metabolites also have potential. More studies must be carried out with larger sample sizes and a standardization of the sampling and processing method. Factors such as diurnal variation, AD patients' decreased ability of oral self-care, and salivary flowrates must be taken into consideration.
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spelling pubmed-65258352019-06-12 Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review Gleerup, Helena Sophia Hasselbalch, Steen Gregers Simonsen, Anja Hviid Dis Markers Review Article BACKGROUND: The histopathological changes of Alzheimer's disease (AD) are detectable decades prior to its clinical expression. However, there is a need for an early, inexpensive, noninvasive diagnostic biomarker to detect specific Alzheimer pathology. Recently developed neuroimaging biomarkers show promising results, but these methods are expensive and cause radiation. Furthermore, the analysis of cerebrospinal fluid (CSF) biomarkers requires an invasive lumbar puncture. Saliva is an easily obtained body fluid, and a stable saliva biomarker would therefore be a promising candidate for a future method for diagnosing AD. The purpose of this systematic review was to investigate studies of biomarkers in saliva samples for the diagnosis of AD. METHODS: The included articles were identified through a literature search in PubMed and Google Scholar for all articles until November 1(st), 2018, and furthermore, all reference lists of included articles were reviewed by hand. We included articles written in English investigating saliva from patients with AD and a control group. RESULTS: A total of 65 studies were identified, whereof 16 studies met the inclusion criteria and were included in the systematic review. A plethora of different biomarkers were investigated, and ten out of the sixteen studies showed a statistical significance in biomarkers between patients with AD and healthy, elderly controls, among these biomarkers for specific AD pathology (amyloid beta 1-42 (Aβ42) and tau). CONCLUSION: Aβ42 and tau seem to be worthy candidates for future salivary biomarkers for AD, but other biomarkers such as lactoferrin and selected metabolites also have potential. More studies must be carried out with larger sample sizes and a standardization of the sampling and processing method. Factors such as diurnal variation, AD patients' decreased ability of oral self-care, and salivary flowrates must be taken into consideration. Hindawi 2019-05-02 /pmc/articles/PMC6525835/ /pubmed/31191751 http://dx.doi.org/10.1155/2019/4761054 Text en Copyright © 2019 Helena Sophia Gleerup et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gleerup, Helena Sophia
Hasselbalch, Steen Gregers
Simonsen, Anja Hviid
Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review
title Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review
title_full Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review
title_fullStr Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review
title_full_unstemmed Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review
title_short Biomarkers for Alzheimer's Disease in Saliva: A Systematic Review
title_sort biomarkers for alzheimer's disease in saliva: a systematic review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525835/
https://www.ncbi.nlm.nih.gov/pubmed/31191751
http://dx.doi.org/10.1155/2019/4761054
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