Lead-grouped multi-stage learning for myocardial infarction localization

IF 4.2 3区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
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 ,&nbsp;Qianyun Zhan ,&nbsp;Jichao Yang ,&nbsp;Ying An ,&nbsp;Jun Long ,&nbsp;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.
心肌梗死定位的导联多阶段学习。
心电图(ECG)是一种普遍存在的医学诊断工具,用于定位以ECG上异常波形模式为特征的心肌梗死(MI)。心肌梗死是一种严重的心血管疾病,准确、及时的诊断对于预防严重后果至关重要。目前的心电分析方法主要依赖于导联内和导联间的特征提取,但大多数模型忽略了与疾病诊断相关的医学知识。此外,现有模型往往不能有效利用多导联心电图的全局空间关系,限制了其全面理解和准确定位MI复杂病理机制的能力。针对这些问题,我们提出了一种知识驱动的重叠导联分组方法。根据临床诊断知识,我们根据与心肌梗死定位的相关性对12根导联进行分组,同时保留整套12根导联作为一个统一的组。此外,我们设计了一个多阶段学习网络,首先通过初始卷积层和渐进卷积块提取基本特征,然后通过se增强的多尺度残差块和位置Transformer块逐步学习更深层次的导内和导间特征。此外,我们提出了一种分支级加权特征集成机制,以有效地融合从每组提取的特征。该方法在公开的多标签PTB-XL数据集上进行了全面评估,对MI定位任务的预测准确率达到80%以上。结果表明,与目前最先进的方法相比,该方法在几个指标上都有显著改善,证实了其卓越的性能。
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 求助全文
来源期刊
Methods
Methods 生物-生化研究方法
CiteScore
9.80
自引率
2.10%
发文量
222
审稿时长
11.3 weeks
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.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信