Lin Guo , Qianyun Zhan , Jichao Yang , Ying An , Jun Long , Nan Ma
{"title":"Lead-grouped multi-stage learning for myocardial infarction localization","authors":"Lin Guo , Qianyun Zhan , Jichao Yang , Ying An , Jun Long , Nan Ma","doi":"10.1016/j.ymeth.2025.01.015","DOIUrl":null,"url":null,"abstract":"<div><div>The electrocardiogram (ECG) is a ubiquitous medical diagnostic tool employed to localize myocardial infarction (MI) that is characterized by abnormal waveform patterns on the ECG. MI is a serious cardiovascular disease, and accurate, timely diagnosis is crucial for preventing severe outcomes. Current ECG analysis methods mainly rely on intra- and inter-lead feature extraction, but most models overlook the medical knowledge relevant to disease diagnosis. Moreover, existing models often fail to effectively utilize the global spatial relationships within multi-lead ECGs, limiting their ability to comprehensively understand and accurately localize the complex pathological mechanisms of MI. To address these issues, we propose a knowledge-driven overlapping lead grouping method. Based on clinical diagnostic knowledge, we group the 12 leads according to their relevance to MI localization while retaining the full set of 12 leads as a unified group. Additionally, we design a multi-stage learning network that first extracts basic features through initial convolutional layer and progressive convolutional block, followed by SE-enhanced multi-scale residual block and positional Transformer block to gradually learn deeper intra- and inter-lead features. Furthermore, we propose a branch-level weighted feature integration mechanism to effectively fuse the features extracted from each group. The proposed method was thoroughly evaluated on the publicly available multi-label PTB-XL dataset and achieved over 80% prediction accuracy for MI localization tasks. The results demonstrated significant improvements across several metrics compared to current state-of-the-art methods, confirming its exceptional performance.</div></div>","PeriodicalId":390,"journal":{"name":"Methods","volume":"234 ","pages":"Pages 315-323"},"PeriodicalIF":4.2000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1046202325000180","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
The electrocardiogram (ECG) is a ubiquitous medical diagnostic tool employed to localize myocardial infarction (MI) that is characterized by abnormal waveform patterns on the ECG. MI is a serious cardiovascular disease, and accurate, timely diagnosis is crucial for preventing severe outcomes. Current ECG analysis methods mainly rely on intra- and inter-lead feature extraction, but most models overlook the medical knowledge relevant to disease diagnosis. Moreover, existing models often fail to effectively utilize the global spatial relationships within multi-lead ECGs, limiting their ability to comprehensively understand and accurately localize the complex pathological mechanisms of MI. To address these issues, we propose a knowledge-driven overlapping lead grouping method. Based on clinical diagnostic knowledge, we group the 12 leads according to their relevance to MI localization while retaining the full set of 12 leads as a unified group. Additionally, we design a multi-stage learning network that first extracts basic features through initial convolutional layer and progressive convolutional block, followed by SE-enhanced multi-scale residual block and positional Transformer block to gradually learn deeper intra- and inter-lead features. Furthermore, we propose a branch-level weighted feature integration mechanism to effectively fuse the features extracted from each group. The proposed method was thoroughly evaluated on the publicly available multi-label PTB-XL dataset and achieved over 80% prediction accuracy for MI localization tasks. The results demonstrated significant improvements across several metrics compared to current state-of-the-art methods, confirming its exceptional performance.
期刊介绍:
Methods focuses on rapidly developing techniques in the experimental biological and medical sciences.
Each topical issue, organized by a guest editor who is an expert in the area covered, consists solely of invited quality articles by specialist authors, many of them reviews. Issues are devoted to specific technical approaches with emphasis on clear detailed descriptions of protocols that allow them to be reproduced easily. The background information provided enables researchers to understand the principles underlying the methods; other helpful sections include comparisons of alternative methods giving the advantages and disadvantages of particular methods, guidance on avoiding potential pitfalls, and suggestions for troubleshooting.