Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/99678
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dc.contributorDepartment of Electrical and Electronic Engineeringen_US
dc.creatorLi, Xen_US
dc.creatorLeung, FHFen_US
dc.creatorSu, Sen_US
dc.creatorLing, SHen_US
dc.date.accessioned2023-07-18T03:14:07Z-
dc.date.available2023-07-18T03:14:07Z-
dc.identifier.urihttp://hdl.handle.net/10397/99678-
dc.language.isoenen_US
dc.publisherMolecular Diversity Preservation International (MDPI)en_US
dc.rights© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).en_US
dc.rightsThe following publication Li, Xilin; Leung, Frank H. F.; Su, Steven; Ling, Sai Ho(2022). Sleep Apnea Detection Using Multi-Error-Reduction Classification System with Multiple Bio-Signals. Sensors, 22(15), 5560 is available at https://doi.org/10.3390/s22155560.en_US
dc.subjectFeature extractionen_US
dc.subjectFeature selectionen_US
dc.subjectPolysomnographyen_US
dc.subjectSleep apnea detectionen_US
dc.titleSleep apnea detection using multi-error-reduction classification system with multiple bio-signalsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume22en_US
dc.identifier.issue15en_US
dc.identifier.doi10.3390/s22155560en_US
dcterms.abstractIntroduction: Obstructive sleep apnea (OSA) can cause serious health problems such as hypertension or cardiovascular disease. The manual detection of apnea is a time-consuming task, and automatic diagnosis is much more desirable. The contribution of this work is to detect OSA using a multi-error-reduction (MER) classification system with multi-domain features from bio-signals. Methods: Time-domain, frequency-domain, and non-linear analysis features are extracted from oxygen saturation (SaO (Formula presented.)), ECG, airflow, thoracic, and abdominal signals. To analyse the significance of each feature, we design a two-stage feature selection. Stage 1 is the statistical analysis stage, and Stage 2 is the final feature subset selection stage using machine learning methods. In Stage 1, two statistical analyses (the one-way analysis of variance (ANOVA) and the rank-sum test) provide a list of the significance level of each kind of feature. Then, in Stage 2, the support vector machine (SVM) algorithm is used to select a final feature subset based on the significance list. Next, an MER classification system is constructed, which applies a stacking with a structure that consists of base learners and an artificial neural network (ANN) meta-learner. Results: The Sleep Heart Health Study (SHHS) database is used to provide bio-signals. A total of 66 features are extracted. In the experiment that involves a duration parameter, 19 features are selected as the final feature subset because they provide a better and more stable performance. The SVM model shows good performance (accuracy = 81.68%, sensitivity = 97.05%, and specificity = 66.54%). It is also found that classifiers have poor performance when they predict normal events in less than 60 s. In the next experiment stage, the time-window segmentation method with a length of 60 s is used. After the above two-stage feature selection procedure, 48 features are selected as the final feature subset that give good performance (accuracy = 90.80%, sensitivity = 93.95%, and specificity = 83.82%). To conduct the classification, Gradient Boosting, CatBoost, Light GBM, and XGBoost are used as base learners, and the ANN is used as the meta-learner. The performance of this MER classification system has the accuracy of 94.66%, the sensitivity of 96.37%, and the specificity of 90.83%.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationSensors, Aug. 2022, v. 22, no. 15, 5560en_US
dcterms.isPartOfSensorsen_US
dcterms.issued2022-08-
dc.identifier.scopus2-s2.0-85135202568-
dc.identifier.eissn1424-8220en_US
dc.identifier.artn5560en_US
dc.description.validate202307 bcwwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera2278-
dc.identifier.SubFormID47308-
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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