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      P-Wave Area Predicts New Onset Atrial Fibrillation in Mitral Stenosis: A Machine Learning Approach

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          Abstract

          Introduction: Mitral stenosis is associated with an atrial cardiomyopathic process, leading to abnormal atrial electrophysiology, manifesting as prolonged P-wave duration (PWD), larger P-wave area, increased P-wave dispersion (PWD max—PWD min), and/or higher P-wave terminal force on lead V1 (PTFV1) on the electrocardiogram.

          Methods: This was a single-center retrospective study of Chinese patients, diagnosed with mitral stenosis in sinus rhythm at baseline, between November 2009 and October 2016. Automated ECG measurements from raw data were determined. The primary outcome was incident atrial fibrillation (AF).

          Results: A total 59 mitral stenosis patients were included (age 59 [54–65] years, 13 (22%) males). New onset AF was observed in 27 patients. Age (odds ratio [OR]: 1.08 [1.01–1.16], P = 0.017), systolic blood pressure (OR: 1.03 [1.00–1.07]; P = 0.046), mean P-wave area in V3 (odds ratio: 3.97 [1.32–11.96], P = 0.014) were significant predictors of incident AF. On multivariate analysis, age (OR: 1.08 [1.00–1.16], P = 0.037) and P-wave area in V3 (OR: 3.64 [1.10–12.00], P = 0.034) remained significant predictors of AF. Receiver-operating characteristic (ROC) analysis showed that the optimum cut-off for P-wave area in V3 was 1.45 Ashman units (area under the curve: 0.65) for classification of new onset AF. A decision tree learning model with individual and non-linear interaction variables with age achieved the best performance for outcome prediction (accuracy = 0.84, precision = 0.84, recall = 0.83, F-measure = 0.84).

          Conclusion: Atrial electrophysiological alterations in mitral stenosis can detected on the electrocardiogram. Age, systolic blood pressure, and P-wave area in V3 predicted new onset AF. A decision tree learning model significantly improved outcome prediction.

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          Most cited references23

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          Interatrial blocks. A separate entity from left atrial enlargement: a consensus report.

          Impaired interatrial conduction or interatrial block is well documented but is not described as an individual electrocardiographic (ECG) pattern in most of ECG books, although the term atrial abnormalities to encompass both concepts, left atrial enlargement (LAE) and interatrial block, has been coined. In fact, LAE and interatrial block are often associated, similarly to what happens with ventricular enlargement and ventricular block. The interatrial blocks, that is, the presence of delay of conduction between the right and left atria, are the most frequent atrial blocks. These may be of first degree (P-wave duration >120 milliseconds), third degree (longer P wave with biphasic [±] morphology in inferior leads), and second degree when these patterns appear transiently in the same ECG recording (atrial aberrancy). There are evidences that these electrocardiographic P-wave patterns are due to a block because they may (a) appear transiently, (b) be without associated atrial enlargement, and (c) may be reproduced experimentally. The presence of interatrial blocks may be seen in the absence of atrial enlargement but often are present in case of LAE. The most important clinical implications of interatrial block are the following: (a) the first degree interatrial blocks are very common, and their relation with atrial fibrillation and an increased risk for global and cardiovascular mortality has been demonstrated; (b) the third degree interatrial blocks are less frequent but are strong markers of LAE and paroxysmal supraventricular tachyarrhythmias. Their presence has been considered a true arrhythmological syndrome. Copyright © 2012 Elsevier Inc. All rights reserved.
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            Association of interatrial block with development of atrial fibrillation.

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              Atrial fibrillation: classification, pathophysiology, mechanisms and drug treatment.

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                Author and article information

                Contributors
                Journal
                Front Bioeng Biotechnol
                Front Bioeng Biotechnol
                Front. Bioeng. Biotechnol.
                Frontiers in Bioengineering and Biotechnology
                Frontiers Media S.A.
                2296-4185
                15 May 2020
                2020
                : 8
                : 479
                Affiliations
                [1] 1Tianjin Key Laboratory of Ionic-Molecular Function of Cardiovascular Disease, Department of Cardiology, Tianjin Institute of Cardiology, Second Hospital of Tianjin Medical University , Tianjin, China
                [2] 2Xiamen Cardiovascular Hospital, Xiamen University , Xiamen, China
                [3] 3Laboratory of Cardiovascular Physiology, Li Ka Shing Institute of Health Sciences , Shatin, China
                [4] 4School of Data Science, City University of Hong Kong , Kowloon, China
                [5] 5Faculty of Medicine, Newcastle University , Newcastle, United Kingdom
                [6] 6Aston Medical School, Aston University , Birmingham, United Kingdom
                [7] 7Heart Rhythm Service, Kingston General Hospital, Queen's University , Kingston, ON, Canada
                Author notes

                Edited by: Wenbing Zhao, Cleveland State University, United States

                Reviewed by: Olaf Doessel, Karlsruhe Institute of Technology (KIT), Germany; Andrew Teh, Eastern Health, Australia

                *Correspondence: Jiandong Zhou jiandzhou3-c@ 123456my.cityu.edu.hk

                This article was submitted to Bioinformatics and Computational Biology, a section of the journal Frontiers in Bioengineering and Biotechnology

                Article
                10.3389/fbioe.2020.00479
                7243705
                32500070
                1426adc0-6879-480b-951b-7d6201e1fead
                Copyright © 2020 Tse, Lakhani, Zhou, Li, Lee, Liu, Leung, Liu, Baranchuk and Zhang.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 21 January 2020
                : 24 April 2020
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 25, Pages: 8, Words: 4772
                Funding
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Award ID: 71972164
                Award ID: 71972164
                Funded by: Health and Medical Research Fund
                Award ID: 16171991
                Categories
                Bioengineering and Biotechnology
                Brief Research Report

                mitral stenosis,mitral valve,p-wave area,decision tree,machine learning

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