Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1128/mSystems.00258-20 http://hdl.handle.net/11449/209528 |
Resumo: | Brazil and many other Latin American countries are areas of endemicity for different neglected diseases, and the fungal infection paracoccidioidomycosis (PCM) is one of them. Among the clinical manifestations, pneumopathy associated with skin and mucosal lesions is the most frequent. PCM definitive diagnosis depends on yeast microscopic visualization and immunological tests, but both present ambiguous results and difficulty in differentiating PCM from other fungal infections. This research has employed metabolomics analysis through high-resolution mass spectrometry to identify PCM biomarkers in serum samples in order to improve diagnosis for this debilitating disease. To upgrade the biomarker selection, machine learning approaches, using Random Forest classifiers, were combined with metabolomics data analysis. The proposed combination of these two analytical methods resulted in the identification of a set of 19 PCM biomarkers that show accuracy of 97.1%, specificity of 100%, and sensitivity of 94.1%. The obtained results are promising and present great potential to improve PCM definitive diagnosis and adequate pharmacological treatment, reducing the incidence of PCM sequelae and resulting in a better quality of life. IMPORTANCE Paracoccidioidomycosis (PCM) is a fungal infection typically found in Latin American countries, especially in Brazil. The identification of this disease is based on techniques that may fail sometimes. Intending to improve PCM detection in patient samples, this study used the combination of two of the newest technologies, artificial intelligence and metabolomics. This combination allowed PCM detection, independently of disease form, through identification of a set of molecules present in patients' blood. The great difference in this research was the ability to detect disease with better confidence than the routine methods employed today. Another important point is that among the molecules, it was possible to identify some indicators of contamination and other infection that might worsen patients' condition. Thus, the present work shows a great potential to improve PCM diagnosis and even disease management, considering the possibility to identify concomitant harmful factors. |
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Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnosesartificial intelligencediagnosismetabolomicsparacoccidioidomycosisBrazil and many other Latin American countries are areas of endemicity for different neglected diseases, and the fungal infection paracoccidioidomycosis (PCM) is one of them. Among the clinical manifestations, pneumopathy associated with skin and mucosal lesions is the most frequent. PCM definitive diagnosis depends on yeast microscopic visualization and immunological tests, but both present ambiguous results and difficulty in differentiating PCM from other fungal infections. This research has employed metabolomics analysis through high-resolution mass spectrometry to identify PCM biomarkers in serum samples in order to improve diagnosis for this debilitating disease. To upgrade the biomarker selection, machine learning approaches, using Random Forest classifiers, were combined with metabolomics data analysis. The proposed combination of these two analytical methods resulted in the identification of a set of 19 PCM biomarkers that show accuracy of 97.1%, specificity of 100%, and sensitivity of 94.1%. The obtained results are promising and present great potential to improve PCM definitive diagnosis and adequate pharmacological treatment, reducing the incidence of PCM sequelae and resulting in a better quality of life. IMPORTANCE Paracoccidioidomycosis (PCM) is a fungal infection typically found in Latin American countries, especially in Brazil. The identification of this disease is based on techniques that may fail sometimes. Intending to improve PCM detection in patient samples, this study used the combination of two of the newest technologies, artificial intelligence and metabolomics. This combination allowed PCM detection, independently of disease form, through identification of a set of molecules present in patients' blood. The great difference in this research was the ability to detect disease with better confidence than the routine methods employed today. Another important point is that among the molecules, it was possible to identify some indicators of contamination and other infection that might worsen patients' condition. Thus, the present work shows a great potential to improve PCM diagnosis and even disease management, considering the possibility to identify concomitant harmful factors.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Sao Paulo State Univ, Botucatu Med Sch, Dept Internal Med, Botucatu, SP, BrazilUniv Estadual Campinas, Sch Pharmaceut Sci, Innovare Biomarkers Lab, Campinas, SP, BrazilUniv Estadual Campinas, Inst Comp, RECOD Lab, Campinas, SP, BrazilAdolfo Lutz Inst, Lab Mycosis Immunodiag, Immunol Sect, Sao Paulo, SP, BrazilSao Paulo State Univ, Botucatu Med Sch, Dept Internal Med, Botucatu, SP, BrazilCAPES: PNPD: 1578388CAPES: PNPD: 88882.305824/2013-01FAPESP: 2018/14657-5FAPESP: 2019/05718-3Amer Soc MicrobiologyUniversidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Adolfo Lutz InstLima, Estela de Oliveira [UNESP]Navarro, Luiz ClaudioMorishita, Karen NodaKamikawa, Camila MikaMartins Rodrigues, Rafael GustavoDabaja, Mohamed ZiadOliveira, Diogo Noin deDelahori, JeanyDias-Audibert, Flavia LuisaRibeiro, Marta da SilvaVicentini, Adriana PardiniRocha, AndersonCatharino, Rodrigo Ramos2021-06-25T12:21:15Z2021-06-25T12:21:15Z2020-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article12http://dx.doi.org/10.1128/mSystems.00258-20Msystems. Washington: Amer Soc Microbiology, v. 5, n. 3, 12 p., 2020.2379-5077http://hdl.handle.net/11449/20952810.1128/mSystems.00258-20WOS:000576704900007Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMsystemsinfo:eu-repo/semantics/openAccess2024-08-14T17:36:42Zoai:repositorio.unesp.br:11449/209528Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-08-14T17:36:42Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses |
title |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses |
spellingShingle |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses Lima, Estela de Oliveira [UNESP] artificial intelligence diagnosis metabolomics paracoccidioidomycosis |
title_short |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses |
title_full |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses |
title_fullStr |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses |
title_full_unstemmed |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses |
title_sort |
Metabolomics and Machine Learning Approaches Combined in Pursuit for More Accurate Paracoccidioidomycosis Diagnoses |
author |
Lima, Estela de Oliveira [UNESP] |
author_facet |
Lima, Estela de Oliveira [UNESP] Navarro, Luiz Claudio Morishita, Karen Noda Kamikawa, Camila Mika Martins Rodrigues, Rafael Gustavo Dabaja, Mohamed Ziad Oliveira, Diogo Noin de Delahori, Jeany Dias-Audibert, Flavia Luisa Ribeiro, Marta da Silva Vicentini, Adriana Pardini Rocha, Anderson Catharino, Rodrigo Ramos |
author_role |
author |
author2 |
Navarro, Luiz Claudio Morishita, Karen Noda Kamikawa, Camila Mika Martins Rodrigues, Rafael Gustavo Dabaja, Mohamed Ziad Oliveira, Diogo Noin de Delahori, Jeany Dias-Audibert, Flavia Luisa Ribeiro, Marta da Silva Vicentini, Adriana Pardini Rocha, Anderson Catharino, Rodrigo Ramos |
author2_role |
author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade Estadual de Campinas (UNICAMP) Adolfo Lutz Inst |
dc.contributor.author.fl_str_mv |
Lima, Estela de Oliveira [UNESP] Navarro, Luiz Claudio Morishita, Karen Noda Kamikawa, Camila Mika Martins Rodrigues, Rafael Gustavo Dabaja, Mohamed Ziad Oliveira, Diogo Noin de Delahori, Jeany Dias-Audibert, Flavia Luisa Ribeiro, Marta da Silva Vicentini, Adriana Pardini Rocha, Anderson Catharino, Rodrigo Ramos |
dc.subject.por.fl_str_mv |
artificial intelligence diagnosis metabolomics paracoccidioidomycosis |
topic |
artificial intelligence diagnosis metabolomics paracoccidioidomycosis |
description |
Brazil and many other Latin American countries are areas of endemicity for different neglected diseases, and the fungal infection paracoccidioidomycosis (PCM) is one of them. Among the clinical manifestations, pneumopathy associated with skin and mucosal lesions is the most frequent. PCM definitive diagnosis depends on yeast microscopic visualization and immunological tests, but both present ambiguous results and difficulty in differentiating PCM from other fungal infections. This research has employed metabolomics analysis through high-resolution mass spectrometry to identify PCM biomarkers in serum samples in order to improve diagnosis for this debilitating disease. To upgrade the biomarker selection, machine learning approaches, using Random Forest classifiers, were combined with metabolomics data analysis. The proposed combination of these two analytical methods resulted in the identification of a set of 19 PCM biomarkers that show accuracy of 97.1%, specificity of 100%, and sensitivity of 94.1%. The obtained results are promising and present great potential to improve PCM definitive diagnosis and adequate pharmacological treatment, reducing the incidence of PCM sequelae and resulting in a better quality of life. IMPORTANCE Paracoccidioidomycosis (PCM) is a fungal infection typically found in Latin American countries, especially in Brazil. The identification of this disease is based on techniques that may fail sometimes. Intending to improve PCM detection in patient samples, this study used the combination of two of the newest technologies, artificial intelligence and metabolomics. This combination allowed PCM detection, independently of disease form, through identification of a set of molecules present in patients' blood. The great difference in this research was the ability to detect disease with better confidence than the routine methods employed today. Another important point is that among the molecules, it was possible to identify some indicators of contamination and other infection that might worsen patients' condition. Thus, the present work shows a great potential to improve PCM diagnosis and even disease management, considering the possibility to identify concomitant harmful factors. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-05-01 2021-06-25T12:21:15Z 2021-06-25T12:21:15Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1128/mSystems.00258-20 Msystems. Washington: Amer Soc Microbiology, v. 5, n. 3, 12 p., 2020. 2379-5077 http://hdl.handle.net/11449/209528 10.1128/mSystems.00258-20 WOS:000576704900007 |
url |
http://dx.doi.org/10.1128/mSystems.00258-20 http://hdl.handle.net/11449/209528 |
identifier_str_mv |
Msystems. Washington: Amer Soc Microbiology, v. 5, n. 3, 12 p., 2020. 2379-5077 10.1128/mSystems.00258-20 WOS:000576704900007 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Msystems |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
12 |
dc.publisher.none.fl_str_mv |
Amer Soc Microbiology |
publisher.none.fl_str_mv |
Amer Soc Microbiology |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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1826304512064749568 |