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The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system

INTRODUCTION: In recent years, there has been an increased demand for computer-aided diagnosis (CAD) tools to support clinicians in the field of indirect immunofluorescence. To this aim, academic and industrial research is focusing on detecting antinuclear, anti-neutrophil, and anti-double-stranded...

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Autores principales: Buzzulini, Francesca, Rigon, Amelia, Soda, Paolo, Onofri, Leonardo, Infantino, Maria, Arcarese, Luisa, Iannello, Giulio, Afeltra, Antonella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060377/
https://www.ncbi.nlm.nih.gov/pubmed/24625089
http://dx.doi.org/10.1186/ar4510
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author Buzzulini, Francesca
Rigon, Amelia
Soda, Paolo
Onofri, Leonardo
Infantino, Maria
Arcarese, Luisa
Iannello, Giulio
Afeltra, Antonella
author_facet Buzzulini, Francesca
Rigon, Amelia
Soda, Paolo
Onofri, Leonardo
Infantino, Maria
Arcarese, Luisa
Iannello, Giulio
Afeltra, Antonella
author_sort Buzzulini, Francesca
collection PubMed
description INTRODUCTION: In recent years, there has been an increased demand for computer-aided diagnosis (CAD) tools to support clinicians in the field of indirect immunofluorescence. To this aim, academic and industrial research is focusing on detecting antinuclear, anti-neutrophil, and anti-double-stranded (anti-dsDNA) antibodies. Within this framework, we present a CAD system for automatic analysis of dsDNA antibody images using a multi-step classification approach. The final classification of a well is based on the classification of all its images, and each image is classified on the basis of the labeling of its cells. METHODS: We populated a database of 342 images—74 positive (21.6%) and 268 negative (78.4%)— belonging to 63 consecutive sera: 15 positive (23.8%) and 48 negative (76.2%). We assessed system performance by using k-fold cross-validation. Furthermore, we successfully validated the recognition system on 83 consecutive sera, collected by using different equipment in a referral center, counting 279 images: 92 positive (33.0%) and 187 negative (67.0%). RESULTS: With respect to well classification, the system correctly classified 98.4% of wells (62 out of 63). Integrating information from multiple images of the same wells recovers the possible misclassifications that occurred at the previous steps (cell and image classification). This system, validated in a clinical routine fashion, provides recognition accuracy equal to 100%. CONCLUSION: The data obtained show that automation is a viable alternative for Crithidia luciliae immunofluorescence test analysis.
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spelling pubmed-40603772014-06-17 The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system Buzzulini, Francesca Rigon, Amelia Soda, Paolo Onofri, Leonardo Infantino, Maria Arcarese, Luisa Iannello, Giulio Afeltra, Antonella Arthritis Res Ther Research Article INTRODUCTION: In recent years, there has been an increased demand for computer-aided diagnosis (CAD) tools to support clinicians in the field of indirect immunofluorescence. To this aim, academic and industrial research is focusing on detecting antinuclear, anti-neutrophil, and anti-double-stranded (anti-dsDNA) antibodies. Within this framework, we present a CAD system for automatic analysis of dsDNA antibody images using a multi-step classification approach. The final classification of a well is based on the classification of all its images, and each image is classified on the basis of the labeling of its cells. METHODS: We populated a database of 342 images—74 positive (21.6%) and 268 negative (78.4%)— belonging to 63 consecutive sera: 15 positive (23.8%) and 48 negative (76.2%). We assessed system performance by using k-fold cross-validation. Furthermore, we successfully validated the recognition system on 83 consecutive sera, collected by using different equipment in a referral center, counting 279 images: 92 positive (33.0%) and 187 negative (67.0%). RESULTS: With respect to well classification, the system correctly classified 98.4% of wells (62 out of 63). Integrating information from multiple images of the same wells recovers the possible misclassifications that occurred at the previous steps (cell and image classification). This system, validated in a clinical routine fashion, provides recognition accuracy equal to 100%. CONCLUSION: The data obtained show that automation is a viable alternative for Crithidia luciliae immunofluorescence test analysis. BioMed Central 2014 2014-03-14 /pmc/articles/PMC4060377/ /pubmed/24625089 http://dx.doi.org/10.1186/ar4510 Text en Copyright © 2014 Buzzulini 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 Research Article
Buzzulini, Francesca
Rigon, Amelia
Soda, Paolo
Onofri, Leonardo
Infantino, Maria
Arcarese, Luisa
Iannello, Giulio
Afeltra, Antonella
The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system
title The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system
title_full The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system
title_fullStr The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system
title_full_unstemmed The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system
title_short The classification of Crithidia luciliae immunofluorescence test (CLIFT) using a novel automated system
title_sort classification of crithidia luciliae immunofluorescence test (clift) using a novel automated system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060377/
https://www.ncbi.nlm.nih.gov/pubmed/24625089
http://dx.doi.org/10.1186/ar4510
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