Automatic Diagnosis of Parkinson Disease through Handwriting Analysis: A Cartesian Genetic Programming Approach

R. Senatore, A. D. Cioppa, A. Marcelli
{"title":"Automatic Diagnosis of Parkinson Disease through Handwriting Analysis: A Cartesian Genetic Programming Approach","authors":"R. Senatore, A. D. Cioppa, A. Marcelli","doi":"10.1109/CBMS.2019.00071","DOIUrl":null,"url":null,"abstract":"Early disease identification through non-invasive and automatic techniques has gathered increasing interest by the scientific community in the last decades. In this context, Parkinsons Disease (PD) has received particular attention in that it is a severe and progressive neurodegenerative disease and, therefore, early diagnosis would provide more prompt and effective intervention strategies. This, in turn, would successfully influence the life expectancy of the patients. However, the acceptance of computer-based diagnosis by doctors is hampered by the black-box approach implemented by the most performing systems, such as Artificial Neural Networks and Support Vector Machines, which do not explicit the rules adopted by the system. In this context, we propose a Cartesian Genetic Programming, aimed at automatically identify PD through the analysis of handwriting performed by PD patients and healthy controls. The use of such approach is particularly interesting in that it allows to infer explicit models of classification and, at same time, to automatically identify a suitable subset of features relevant for a correct diagnosis. The approach has been evaluated on the features extracted from the handwriting samples contained in the publicly available PaHaW dataset. Experimental results show that our approach compares favorably with state-of-the-art methods and, more importantly, provides an explicit model of the classification criteria.","PeriodicalId":311634,"journal":{"name":"2019 IEEE 32nd International Symposium on Computer-Based Medical Systems (CBMS)","volume":"11 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2019 IEEE 32nd International Symposium on Computer-Based Medical Systems (CBMS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/CBMS.2019.00071","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 14

Abstract

Early disease identification through non-invasive and automatic techniques has gathered increasing interest by the scientific community in the last decades. In this context, Parkinsons Disease (PD) has received particular attention in that it is a severe and progressive neurodegenerative disease and, therefore, early diagnosis would provide more prompt and effective intervention strategies. This, in turn, would successfully influence the life expectancy of the patients. However, the acceptance of computer-based diagnosis by doctors is hampered by the black-box approach implemented by the most performing systems, such as Artificial Neural Networks and Support Vector Machines, which do not explicit the rules adopted by the system. In this context, we propose a Cartesian Genetic Programming, aimed at automatically identify PD through the analysis of handwriting performed by PD patients and healthy controls. The use of such approach is particularly interesting in that it allows to infer explicit models of classification and, at same time, to automatically identify a suitable subset of features relevant for a correct diagnosis. The approach has been evaluated on the features extracted from the handwriting samples contained in the publicly available PaHaW dataset. Experimental results show that our approach compares favorably with state-of-the-art methods and, more importantly, provides an explicit model of the classification criteria.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过笔迹分析来自动诊断帕金森病:一种笛卡尔遗传规划方法
在过去的几十年里,通过非侵入性和自动技术进行早期疾病识别已经引起了科学界越来越大的兴趣。在这种背景下,帕金森病(PD)受到了特别的关注,因为它是一种严重的进行性神经退行性疾病,因此,早期诊断将提供更及时有效的干预策略。反过来,这将成功地影响患者的预期寿命。然而,大多数表现良好的系统(如人工神经网络和支持向量机)所采用的黑盒方法阻碍了医生接受基于计算机的诊断,这些系统没有明确规定系统所采用的规则。在此背景下,我们提出了一种笛卡尔遗传规划,旨在通过分析PD患者和健康对照者的笔迹来自动识别PD。这种方法的使用特别有趣,因为它允许推断明确的分类模型,同时,自动识别与正确诊断相关的适当特征子集。该方法已经在从公开可用的PaHaW数据集中包含的手写样本中提取的特征上进行了评估。实验结果表明,我们的方法优于最先进的方法,更重要的是,提供了一个明确的分类标准模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Analysing the Performance of a Real-Time Healthcare 4.0 System using Shared Frailty Time to Event Models Performance of Data Enhancements and Training Optimization for Neural Network: A Polyp Detection Case Study I Know How you Feel Now, and Here's why!: Demystifying Time-Continuous High Resolution Text-Based Affect Predictions in the Wild Identifying Diabetic Retinopathy from OCT Images using Deep Transfer Learning with Artificial Neural Networks Towards an Analysis of Post-Transcriptional Gene Regulation in Psoriasis via microRNAs using Machine Learning Algorithms
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1