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Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion

BACKGROUND: Alzheimer’s disease (AD) remains to date an incurable disease with a long asymptomatic phase. Early diagnosis in peripheral biofluids has emerged as key for identifying subjects at risk and developing therapeutics and preventative approaches. OBJECTIVE: We apply proteomics discovery to i...

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Autores principales: Eldem, Ece, Barve, Aatmika, Sallin, Olivier, Foucras, Sandrine, Annoni, Jean-Marie, Schmid, Adrien W., Alberi Auber, Lavinia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925122/
https://www.ncbi.nlm.nih.gov/pubmed/35360272
http://dx.doi.org/10.3233/ADR-210056
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author Eldem, Ece
Barve, Aatmika
Sallin, Olivier
Foucras, Sandrine
Annoni, Jean-Marie
Schmid, Adrien W.
Alberi Auber, Lavinia
author_facet Eldem, Ece
Barve, Aatmika
Sallin, Olivier
Foucras, Sandrine
Annoni, Jean-Marie
Schmid, Adrien W.
Alberi Auber, Lavinia
author_sort Eldem, Ece
collection PubMed
description BACKGROUND: Alzheimer’s disease (AD) remains to date an incurable disease with a long asymptomatic phase. Early diagnosis in peripheral biofluids has emerged as key for identifying subjects at risk and developing therapeutics and preventative approaches. OBJECTIVE: We apply proteomics discovery to identify salivary diagnostic biomarkers for AD, which are suitable for self-sampling and longitudinal biomonitoring during aging. METHODS: 57 participants were recruited for the study and were categorized into Cognitively normal (CNh) (n = 19), mild cognitive impaired (MCI) (n = 21), and Alzheimer’s disease (AD) (n = 17). On a subset of subjects, 3 CNh and 3 mild AD, shot-gun filter aided sample preparation (FASP) proteomics and liquid chromatography mass spectroscopy (LC-MS/MS) was employed in saliva and cerebrospinal fluid (CSF) to identify neural-derived proteins. The protein level of salivary Transthyretin (TTR) was validated using western blot analysis across groups. RESULTS: We found that 19.8% of the proteins in saliva are shared with CSF. When we compared the saliva and CSF proteome, 24 hits were decreased with only one protein expressed more. Among the differentially expressed proteins, TTR with reported function in amyloid misfolding, shows a significant drop in AD samples, confirmed by western blot showing a 0.5-fold reduction in MCI and AD compared to CNh. CONCLUSION: A reduction in salivary TTR appears with the onset of cognitive symptoms. More in general, the proteomic profiling of saliva shows a plethora of biomarkers worth pursuing as non-invasive hallmarks of dementia in the preclinical stage.
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spelling pubmed-89251222022-03-30 Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion Eldem, Ece Barve, Aatmika Sallin, Olivier Foucras, Sandrine Annoni, Jean-Marie Schmid, Adrien W. Alberi Auber, Lavinia J Alzheimers Dis Rep Research Report BACKGROUND: Alzheimer’s disease (AD) remains to date an incurable disease with a long asymptomatic phase. Early diagnosis in peripheral biofluids has emerged as key for identifying subjects at risk and developing therapeutics and preventative approaches. OBJECTIVE: We apply proteomics discovery to identify salivary diagnostic biomarkers for AD, which are suitable for self-sampling and longitudinal biomonitoring during aging. METHODS: 57 participants were recruited for the study and were categorized into Cognitively normal (CNh) (n = 19), mild cognitive impaired (MCI) (n = 21), and Alzheimer’s disease (AD) (n = 17). On a subset of subjects, 3 CNh and 3 mild AD, shot-gun filter aided sample preparation (FASP) proteomics and liquid chromatography mass spectroscopy (LC-MS/MS) was employed in saliva and cerebrospinal fluid (CSF) to identify neural-derived proteins. The protein level of salivary Transthyretin (TTR) was validated using western blot analysis across groups. RESULTS: We found that 19.8% of the proteins in saliva are shared with CSF. When we compared the saliva and CSF proteome, 24 hits were decreased with only one protein expressed more. Among the differentially expressed proteins, TTR with reported function in amyloid misfolding, shows a significant drop in AD samples, confirmed by western blot showing a 0.5-fold reduction in MCI and AD compared to CNh. CONCLUSION: A reduction in salivary TTR appears with the onset of cognitive symptoms. More in general, the proteomic profiling of saliva shows a plethora of biomarkers worth pursuing as non-invasive hallmarks of dementia in the preclinical stage. IOS Press 2022-02-02 /pmc/articles/PMC8925122/ /pubmed/35360272 http://dx.doi.org/10.3233/ADR-210056 Text en © 2022 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://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 Research Report
Eldem, Ece
Barve, Aatmika
Sallin, Olivier
Foucras, Sandrine
Annoni, Jean-Marie
Schmid, Adrien W.
Alberi Auber, Lavinia
Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion
title Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion
title_full Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion
title_fullStr Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion
title_full_unstemmed Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion
title_short Salivary Proteomics Identifies Transthyretin as a Biomarker of Early Dementia Conversion
title_sort salivary proteomics identifies transthyretin as a biomarker of early dementia conversion
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925122/
https://www.ncbi.nlm.nih.gov/pubmed/35360272
http://dx.doi.org/10.3233/ADR-210056
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