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Tear fluid proteomics multimarkers for diabetic retinopathy screening

BACKGROUND: The aim of the project was to develop a novel method for diabetic retinopathy screening based on the examination of tear fluid biomarker changes. In order to evaluate the usability of protein biomarkers for pre-screening purposes several different approaches were used, including machine...

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Autores principales: Torok, Zsolt, Peto, Tunde, Csosz, Eva, Tukacs, Edit, Molnar, Agnes, Maros-Szabo, Zsuzsanna, Berta, Andras, Tozser, Jozsef, Hajdu, Andras, Nagy, Valeria, Domokos, Balint, Csutak, Adrienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770351/
https://www.ncbi.nlm.nih.gov/pubmed/23919537
http://dx.doi.org/10.1186/1471-2415-13-40
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author Torok, Zsolt
Peto, Tunde
Csosz, Eva
Tukacs, Edit
Molnar, Agnes
Maros-Szabo, Zsuzsanna
Berta, Andras
Tozser, Jozsef
Hajdu, Andras
Nagy, Valeria
Domokos, Balint
Csutak, Adrienne
author_facet Torok, Zsolt
Peto, Tunde
Csosz, Eva
Tukacs, Edit
Molnar, Agnes
Maros-Szabo, Zsuzsanna
Berta, Andras
Tozser, Jozsef
Hajdu, Andras
Nagy, Valeria
Domokos, Balint
Csutak, Adrienne
author_sort Torok, Zsolt
collection PubMed
description BACKGROUND: The aim of the project was to develop a novel method for diabetic retinopathy screening based on the examination of tear fluid biomarker changes. In order to evaluate the usability of protein biomarkers for pre-screening purposes several different approaches were used, including machine learning algorithms. METHODS: All persons involved in the study had diabetes. Diabetic retinopathy (DR) was diagnosed by capturing 7-field fundus images, evaluated by two independent ophthalmologists. 165 eyes were examined (from 119 patients), 55 were diagnosed healthy and 110 images showed signs of DR. Tear samples were taken from all eyes and state-of-the-art nano-HPLC coupled ESI-MS/MS mass spectrometry protein identification was performed on all samples. Applicability of protein biomarkers was evaluated by six different optimally parameterized machine learning algorithms: Support Vector Machine, Recursive Partitioning, Random Forest, Naive Bayes, Logistic Regression, K-Nearest Neighbor. RESULTS: Out of the six investigated machine learning algorithms the result of Recursive Partitioning proved to be the most accurate. The performance of the system realizing the above algorithm reached 74% sensitivity and 48% specificity. CONCLUSIONS: Protein biomarkers selected and classified with machine learning algorithms alone are at present not recommended for screening purposes because of low specificity and sensitivity values. This tool can be potentially used to improve the results of image processing methods as a complementary tool in automatic or semiautomatic systems.
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spelling pubmed-37703512013-09-12 Tear fluid proteomics multimarkers for diabetic retinopathy screening Torok, Zsolt Peto, Tunde Csosz, Eva Tukacs, Edit Molnar, Agnes Maros-Szabo, Zsuzsanna Berta, Andras Tozser, Jozsef Hajdu, Andras Nagy, Valeria Domokos, Balint Csutak, Adrienne BMC Ophthalmol Technical Advance BACKGROUND: The aim of the project was to develop a novel method for diabetic retinopathy screening based on the examination of tear fluid biomarker changes. In order to evaluate the usability of protein biomarkers for pre-screening purposes several different approaches were used, including machine learning algorithms. METHODS: All persons involved in the study had diabetes. Diabetic retinopathy (DR) was diagnosed by capturing 7-field fundus images, evaluated by two independent ophthalmologists. 165 eyes were examined (from 119 patients), 55 were diagnosed healthy and 110 images showed signs of DR. Tear samples were taken from all eyes and state-of-the-art nano-HPLC coupled ESI-MS/MS mass spectrometry protein identification was performed on all samples. Applicability of protein biomarkers was evaluated by six different optimally parameterized machine learning algorithms: Support Vector Machine, Recursive Partitioning, Random Forest, Naive Bayes, Logistic Regression, K-Nearest Neighbor. RESULTS: Out of the six investigated machine learning algorithms the result of Recursive Partitioning proved to be the most accurate. The performance of the system realizing the above algorithm reached 74% sensitivity and 48% specificity. CONCLUSIONS: Protein biomarkers selected and classified with machine learning algorithms alone are at present not recommended for screening purposes because of low specificity and sensitivity values. This tool can be potentially used to improve the results of image processing methods as a complementary tool in automatic or semiautomatic systems. BioMed Central 2013-08-07 /pmc/articles/PMC3770351/ /pubmed/23919537 http://dx.doi.org/10.1186/1471-2415-13-40 Text en Copyright © 2013 Torok et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Advance
Torok, Zsolt
Peto, Tunde
Csosz, Eva
Tukacs, Edit
Molnar, Agnes
Maros-Szabo, Zsuzsanna
Berta, Andras
Tozser, Jozsef
Hajdu, Andras
Nagy, Valeria
Domokos, Balint
Csutak, Adrienne
Tear fluid proteomics multimarkers for diabetic retinopathy screening
title Tear fluid proteomics multimarkers for diabetic retinopathy screening
title_full Tear fluid proteomics multimarkers for diabetic retinopathy screening
title_fullStr Tear fluid proteomics multimarkers for diabetic retinopathy screening
title_full_unstemmed Tear fluid proteomics multimarkers for diabetic retinopathy screening
title_short Tear fluid proteomics multimarkers for diabetic retinopathy screening
title_sort tear fluid proteomics multimarkers for diabetic retinopathy screening
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770351/
https://www.ncbi.nlm.nih.gov/pubmed/23919537
http://dx.doi.org/10.1186/1471-2415-13-40
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