Cargando…

Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial

BACKGROUND: Diagnosis of neuromuscular diseases in primary care is often challenging. Rare diseases such as Pompe disease are easily overlooked by the general practitioner. We therefore aimed to develop a diagnostic support tool using patient-oriented questions and combined data mining algorithms re...

Descripción completa

Detalles Bibliográficos
Autores principales: Grigull, Lorenz, Lechner, Werner, Petri, Susanne, Kollewe, Katja, Dengler, Reinhard, Mehmecke, Sandra, Schumacher, Ulrike, Lücke, Thomas, Schneider-Gold, Christiane, Köhler, Cornelia, Güttsches, Anne-Katrin, Kortum, Xiaowei, Klawonn, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782522/
https://www.ncbi.nlm.nih.gov/pubmed/26957320
http://dx.doi.org/10.1186/s12911-016-0268-5
_version_ 1782419976544583680
author Grigull, Lorenz
Lechner, Werner
Petri, Susanne
Kollewe, Katja
Dengler, Reinhard
Mehmecke, Sandra
Schumacher, Ulrike
Lücke, Thomas
Schneider-Gold, Christiane
Köhler, Cornelia
Güttsches, Anne-Katrin
Kortum, Xiaowei
Klawonn, Frank
author_facet Grigull, Lorenz
Lechner, Werner
Petri, Susanne
Kollewe, Katja
Dengler, Reinhard
Mehmecke, Sandra
Schumacher, Ulrike
Lücke, Thomas
Schneider-Gold, Christiane
Köhler, Cornelia
Güttsches, Anne-Katrin
Kortum, Xiaowei
Klawonn, Frank
author_sort Grigull, Lorenz
collection PubMed
description BACKGROUND: Diagnosis of neuromuscular diseases in primary care is often challenging. Rare diseases such as Pompe disease are easily overlooked by the general practitioner. We therefore aimed to develop a diagnostic support tool using patient-oriented questions and combined data mining algorithms recognizing answer patterns in individuals with selected neuromuscular diseases. A multicenter prospective study for the proof of concept was conducted thereafter. METHODS: First, 16 interviews with patients were conducted focusing on their pre-diagnostic observations and experiences. From these interviews, we developed a questionnaire with 46 items. Then, patients with diagnosed neuromuscular diseases as well as patients without such a disease answered the questionnaire to establish a database for data mining. For proof of concept, initially only six diagnoses were chosen (myotonic dystrophy and myotonia (MdMy), Pompe disease (MP), amyotrophic lateral sclerosis (ALS), polyneuropathy (PNP), spinal muscular atrophy (SMA), other neuromuscular diseases, and no neuromuscular disease (NND). A prospective study was performed to validate the automated malleable system, which included six different classification methods combined in a fusion algorithm proposing a final diagnosis. Finally, new diagnoses were incorporated into the system. RESULTS: In total, questionnaires from 210 individuals were used to train the system. 89.5 % correct diagnoses were achieved during cross-validation. The sensitivity of the system was 93–97 % for individuals with MP, with MdMy and without neuromuscular diseases, but only 69 % in SMA and 81 % in ALS patients. In the prospective trial, 57/64 (89 %) diagnoses were predicted correctly by the computerized system. All questions, or rather all answers, increased the diagnostic accuracy of the system, with the best results reached by the fusion of different classifier methods. Receiver operating curve (ROC) and p-value analyses confirmed the results. CONCLUSION: A questionnaire-based diagnostic support tool using data mining methods exhibited good results in predicting selected neuromuscular diseases. Due to the variety of neuromuscular diseases, additional studies are required to measure beneficial effects in the clinical setting. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12911-016-0268-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4782522
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-47825222016-03-09 Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial Grigull, Lorenz Lechner, Werner Petri, Susanne Kollewe, Katja Dengler, Reinhard Mehmecke, Sandra Schumacher, Ulrike Lücke, Thomas Schneider-Gold, Christiane Köhler, Cornelia Güttsches, Anne-Katrin Kortum, Xiaowei Klawonn, Frank BMC Med Inform Decis Mak Research Article BACKGROUND: Diagnosis of neuromuscular diseases in primary care is often challenging. Rare diseases such as Pompe disease are easily overlooked by the general practitioner. We therefore aimed to develop a diagnostic support tool using patient-oriented questions and combined data mining algorithms recognizing answer patterns in individuals with selected neuromuscular diseases. A multicenter prospective study for the proof of concept was conducted thereafter. METHODS: First, 16 interviews with patients were conducted focusing on their pre-diagnostic observations and experiences. From these interviews, we developed a questionnaire with 46 items. Then, patients with diagnosed neuromuscular diseases as well as patients without such a disease answered the questionnaire to establish a database for data mining. For proof of concept, initially only six diagnoses were chosen (myotonic dystrophy and myotonia (MdMy), Pompe disease (MP), amyotrophic lateral sclerosis (ALS), polyneuropathy (PNP), spinal muscular atrophy (SMA), other neuromuscular diseases, and no neuromuscular disease (NND). A prospective study was performed to validate the automated malleable system, which included six different classification methods combined in a fusion algorithm proposing a final diagnosis. Finally, new diagnoses were incorporated into the system. RESULTS: In total, questionnaires from 210 individuals were used to train the system. 89.5 % correct diagnoses were achieved during cross-validation. The sensitivity of the system was 93–97 % for individuals with MP, with MdMy and without neuromuscular diseases, but only 69 % in SMA and 81 % in ALS patients. In the prospective trial, 57/64 (89 %) diagnoses were predicted correctly by the computerized system. All questions, or rather all answers, increased the diagnostic accuracy of the system, with the best results reached by the fusion of different classifier methods. Receiver operating curve (ROC) and p-value analyses confirmed the results. CONCLUSION: A questionnaire-based diagnostic support tool using data mining methods exhibited good results in predicting selected neuromuscular diseases. Due to the variety of neuromuscular diseases, additional studies are required to measure beneficial effects in the clinical setting. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12911-016-0268-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-08 /pmc/articles/PMC4782522/ /pubmed/26957320 http://dx.doi.org/10.1186/s12911-016-0268-5 Text en © Grigull et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Grigull, Lorenz
Lechner, Werner
Petri, Susanne
Kollewe, Katja
Dengler, Reinhard
Mehmecke, Sandra
Schumacher, Ulrike
Lücke, Thomas
Schneider-Gold, Christiane
Köhler, Cornelia
Güttsches, Anne-Katrin
Kortum, Xiaowei
Klawonn, Frank
Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial
title Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial
title_full Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial
title_fullStr Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial
title_full_unstemmed Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial
title_short Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial
title_sort diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782522/
https://www.ncbi.nlm.nih.gov/pubmed/26957320
http://dx.doi.org/10.1186/s12911-016-0268-5
work_keys_str_mv AT grigulllorenz diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT lechnerwerner diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT petrisusanne diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT kollewekatja diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT denglerreinhard diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT mehmeckesandra diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT schumacherulrike diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT luckethomas diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT schneidergoldchristiane diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT kohlercornelia diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT guttschesannekatrin diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT kortumxiaowei diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial
AT klawonnfrank diagnosticsupportforselectedneuromusculardiseasesusinganswerpatternrecognitionanddataminingtechniquesaproofofconceptmulticenterprospectivetrial