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Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin

INTRODUCTION: The Alzheimer's disease (AD) process is likely initiated many years before clinical onset. Biomarkers of preclinical disease are critical for the development of disease-modifying or even preventative therapies. Current biomarkers for early disease, including cerebrospinal fluid ta...

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Autores principales: Carro, Eva, Bartolomé, Fernando, Bermejo-Pareja, Félix, Villarejo-Galende, Alberto, Molina, José Antonio, Ortiz, Pablo, Calero, Miguel, Rabano, Alberto, Cantero, José Luis, Orive, Gorka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470603/
https://www.ncbi.nlm.nih.gov/pubmed/28649597
http://dx.doi.org/10.1016/j.dadm.2017.04.002
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author Carro, Eva
Bartolomé, Fernando
Bermejo-Pareja, Félix
Villarejo-Galende, Alberto
Molina, José Antonio
Ortiz, Pablo
Calero, Miguel
Rabano, Alberto
Cantero, José Luis
Orive, Gorka
author_facet Carro, Eva
Bartolomé, Fernando
Bermejo-Pareja, Félix
Villarejo-Galende, Alberto
Molina, José Antonio
Ortiz, Pablo
Calero, Miguel
Rabano, Alberto
Cantero, José Luis
Orive, Gorka
author_sort Carro, Eva
collection PubMed
description INTRODUCTION: The Alzheimer's disease (AD) process is likely initiated many years before clinical onset. Biomarkers of preclinical disease are critical for the development of disease-modifying or even preventative therapies. Current biomarkers for early disease, including cerebrospinal fluid tau and amyloid β (Aβ) levels, structural and functional magnetic resonance imaging, and the use of brain amyloid imaging, are limited because they are very invasive or expensive. Noninvasive biomarkers may be a more accessible alternative, but none can currently detect preclinical AD with the required sensitivity and specificity. METHODS: Here, we show a novel, straight-forward, and noninvasive approach for assessment of early stages of cognitive decline. Salivary samples from cases of amnestic mild cognitive impairment (aMCI) and AD, and neurology controls were analyzed. RESULTS: We have discovered and validated a new single saliva biomarker, lactoferrin, which in our cross-sectional investigation perfectly discriminates clinically diagnosed aMCI and AD patients from a cognitively healthy control group. The accuracy for AD diagnosis shown by salivary lactoferrin was greater than that obtained from core cerebrospinal fluid (CSF) biomarkers, including total tau and CSF Aβ(42). Furthermore, salivary lactoferrin can be used for population screening and for identifying those underdiagnosed subjects with very early stages of mild cognitive impairment and AD. CONCLUSION: This biomarker may offer new insights in the early diagnostics for AD.
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spelling pubmed-54706032017-06-23 Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin Carro, Eva Bartolomé, Fernando Bermejo-Pareja, Félix Villarejo-Galende, Alberto Molina, José Antonio Ortiz, Pablo Calero, Miguel Rabano, Alberto Cantero, José Luis Orive, Gorka Alzheimers Dement (Amst) Diagnostic Assessment & Prognosis INTRODUCTION: The Alzheimer's disease (AD) process is likely initiated many years before clinical onset. Biomarkers of preclinical disease are critical for the development of disease-modifying or even preventative therapies. Current biomarkers for early disease, including cerebrospinal fluid tau and amyloid β (Aβ) levels, structural and functional magnetic resonance imaging, and the use of brain amyloid imaging, are limited because they are very invasive or expensive. Noninvasive biomarkers may be a more accessible alternative, but none can currently detect preclinical AD with the required sensitivity and specificity. METHODS: Here, we show a novel, straight-forward, and noninvasive approach for assessment of early stages of cognitive decline. Salivary samples from cases of amnestic mild cognitive impairment (aMCI) and AD, and neurology controls were analyzed. RESULTS: We have discovered and validated a new single saliva biomarker, lactoferrin, which in our cross-sectional investigation perfectly discriminates clinically diagnosed aMCI and AD patients from a cognitively healthy control group. The accuracy for AD diagnosis shown by salivary lactoferrin was greater than that obtained from core cerebrospinal fluid (CSF) biomarkers, including total tau and CSF Aβ(42). Furthermore, salivary lactoferrin can be used for population screening and for identifying those underdiagnosed subjects with very early stages of mild cognitive impairment and AD. CONCLUSION: This biomarker may offer new insights in the early diagnostics for AD. Elsevier 2017-05-26 /pmc/articles/PMC5470603/ /pubmed/28649597 http://dx.doi.org/10.1016/j.dadm.2017.04.002 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Diagnostic Assessment & Prognosis
Carro, Eva
Bartolomé, Fernando
Bermejo-Pareja, Félix
Villarejo-Galende, Alberto
Molina, José Antonio
Ortiz, Pablo
Calero, Miguel
Rabano, Alberto
Cantero, José Luis
Orive, Gorka
Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin
title Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin
title_full Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin
title_fullStr Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin
title_full_unstemmed Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin
title_short Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin
title_sort early diagnosis of mild cognitive impairment and alzheimer's disease based on salivary lactoferrin
topic Diagnostic Assessment & Prognosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470603/
https://www.ncbi.nlm.nih.gov/pubmed/28649597
http://dx.doi.org/10.1016/j.dadm.2017.04.002
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