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Tear-Based Vibrational Spectroscopy Applied to Amyotrophic Lateral Sclerosis
[Image: see text] Biofluid analysis by optical spectroscopy techniques is attracting considerable interest due to its potential to revolutionize diagnostics and precision medicine, particularly for neurodegenerative diseases. However, the lack of effective biomarkers combined with the unaccomplished...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8717331/ https://www.ncbi.nlm.nih.gov/pubmed/34905686 http://dx.doi.org/10.1021/acs.analchem.1c02546 |
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author | Ami, Diletta Duse, Alessandro Mereghetti, Paolo Cozza, Federica Ambrosio, Francesca Ponzini, Erika Grandori, Rita Lunetta, Christian Tavazzi, Silvia Pezzoli, Fabio Natalello, Antonino |
author_facet | Ami, Diletta Duse, Alessandro Mereghetti, Paolo Cozza, Federica Ambrosio, Francesca Ponzini, Erika Grandori, Rita Lunetta, Christian Tavazzi, Silvia Pezzoli, Fabio Natalello, Antonino |
author_sort | Ami, Diletta |
collection | PubMed |
description | [Image: see text] Biofluid analysis by optical spectroscopy techniques is attracting considerable interest due to its potential to revolutionize diagnostics and precision medicine, particularly for neurodegenerative diseases. However, the lack of effective biomarkers combined with the unaccomplished identification of convenient biofluids has drastically hampered optical advancements in clinical diagnosis and monitoring of neurodegenerative disorders. Here, we show that vibrational spectroscopy applied to human tears opens a new route, offering a non-invasive, label-free identification of a devastating disease such as amyotrophic lateral sclerosis (ALS). Our proposed approach has been validated using two widespread techniques, namely, Fourier transform infrared (FTIR) and Raman microspectroscopies. In conjunction with multivariate analysis, this vibrational approach made it possible to discriminate between tears from ALS patients and healthy controls (HCs) with high specificity (∼97% and ∼100% for FTIR and Raman spectroscopy, respectively) and sensitivity (∼88% and ∼100% for FTIR and Raman spectroscopy, respectively). Additionally, the investigation of tears allowed us to disclose ALS spectroscopic markers related to protein and lipid alterations, as well as to a reduction of the phenylalanine level, in comparison with HCs. Our findings show that vibrational spectroscopy is a new potential ALS diagnostic approach and indicate that tears are a reliable and non-invasive source of ALS biomarkers. |
format | Online Article Text |
id | pubmed-8717331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-87173312021-12-30 Tear-Based Vibrational Spectroscopy Applied to Amyotrophic Lateral Sclerosis Ami, Diletta Duse, Alessandro Mereghetti, Paolo Cozza, Federica Ambrosio, Francesca Ponzini, Erika Grandori, Rita Lunetta, Christian Tavazzi, Silvia Pezzoli, Fabio Natalello, Antonino Anal Chem [Image: see text] Biofluid analysis by optical spectroscopy techniques is attracting considerable interest due to its potential to revolutionize diagnostics and precision medicine, particularly for neurodegenerative diseases. However, the lack of effective biomarkers combined with the unaccomplished identification of convenient biofluids has drastically hampered optical advancements in clinical diagnosis and monitoring of neurodegenerative disorders. Here, we show that vibrational spectroscopy applied to human tears opens a new route, offering a non-invasive, label-free identification of a devastating disease such as amyotrophic lateral sclerosis (ALS). Our proposed approach has been validated using two widespread techniques, namely, Fourier transform infrared (FTIR) and Raman microspectroscopies. In conjunction with multivariate analysis, this vibrational approach made it possible to discriminate between tears from ALS patients and healthy controls (HCs) with high specificity (∼97% and ∼100% for FTIR and Raman spectroscopy, respectively) and sensitivity (∼88% and ∼100% for FTIR and Raman spectroscopy, respectively). Additionally, the investigation of tears allowed us to disclose ALS spectroscopic markers related to protein and lipid alterations, as well as to a reduction of the phenylalanine level, in comparison with HCs. Our findings show that vibrational spectroscopy is a new potential ALS diagnostic approach and indicate that tears are a reliable and non-invasive source of ALS biomarkers. American Chemical Society 2021-12-14 2021-12-28 /pmc/articles/PMC8717331/ /pubmed/34905686 http://dx.doi.org/10.1021/acs.analchem.1c02546 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ami, Diletta Duse, Alessandro Mereghetti, Paolo Cozza, Federica Ambrosio, Francesca Ponzini, Erika Grandori, Rita Lunetta, Christian Tavazzi, Silvia Pezzoli, Fabio Natalello, Antonino Tear-Based Vibrational Spectroscopy Applied to Amyotrophic Lateral Sclerosis |
title | Tear-Based Vibrational Spectroscopy Applied to Amyotrophic
Lateral Sclerosis |
title_full | Tear-Based Vibrational Spectroscopy Applied to Amyotrophic
Lateral Sclerosis |
title_fullStr | Tear-Based Vibrational Spectroscopy Applied to Amyotrophic
Lateral Sclerosis |
title_full_unstemmed | Tear-Based Vibrational Spectroscopy Applied to Amyotrophic
Lateral Sclerosis |
title_short | Tear-Based Vibrational Spectroscopy Applied to Amyotrophic
Lateral Sclerosis |
title_sort | tear-based vibrational spectroscopy applied to amyotrophic
lateral sclerosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8717331/ https://www.ncbi.nlm.nih.gov/pubmed/34905686 http://dx.doi.org/10.1021/acs.analchem.1c02546 |
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