James A. Coleman , Julia Camps , Abdallah I. Hasaballa , Alfonso Bueno-Orovio
{"title":"基于仿真的心电图激活和复极序列的数字孪生横跨健康和患病心脏。","authors":"James A. Coleman , Julia Camps , Abdallah I. Hasaballa , Alfonso Bueno-Orovio","doi":"10.1016/j.compbiomed.2025.111222","DOIUrl":null,"url":null,"abstract":"<div><div>Abnormal patterns of ventricular repolarisation are thought to contribute to lethal arrhythmias in various cardiac conditions, including inherited and acquired channelopathies, cardiomyopathies, and ischaemic heart disease. However, methods to detect these repolarisation abnormalities are limited.</div><div>In this study, we introduce and assess a novel simulation-based method to infer ventricular activation and repolarisation times from the 12-lead electrocardiogram (ECG) and magnetic resonance-derived ventricular anatomical reconstruction, applicable for the first time to both healthy controls and cases with abnormal repolarisation.</div><div>First, ventricular activation times were reconstructed through iterative refinement of early activation sites and conduction velocities, until the model and target QRS complexes matched. Then, ventricular repolarisation times were reconstructed through iterative refinement of ventricular action potential durations and an action potential shape parameter until the model and target T waves matched, including regularisation. Repolarisation inference was evaluated against 18 benchmark simulations with known repolarisation times, including both control and hypertrophic cardiomyopathy (HCM) cases with abnormal repolarisation.</div><div>Inferred repolarisation times showed good agreement with the ground truth in control and HCM (Spearman <span><math><mrow><mi>r</mi><mo>=</mo><mn>0.63</mn><mo>±</mo><mn>0.11</mn></mrow></math></span> and <span><math><mrow><mn>0.65</mn><mo>±</mo><mn>0.19</mn></mrow></math></span>, respectively), with the inferred model T waves closely matching the target T waves (<span><math><mrow><mi>r</mi><mo>=</mo><mn>0.81</mn><mo>±</mo><mn>0.05</mn></mrow></math></span> and <span><math><mrow><mn>0.78</mn><mo>±</mo><mn>0.08</mn></mrow></math></span>, respectively). The method further demonstrated flexibility in reconstructing the macroscopic patterns of delayed repolarisation across a range of abnormal ventricular repolarisation sequences, demonstrating applicability to a wide range of pathological scenarios.</div><div>Simulation-based inference can accurately reconstruct repolarisation times from the 12-lead ECG in cases with both normal and abnormal repolarisation patterns.</div></div>","PeriodicalId":10578,"journal":{"name":"Computers in biology and medicine","volume":"198 ","pages":"Article 111222"},"PeriodicalIF":6.3000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Simulation-based digital twinning of activation and repolarisation sequences from the ECG across healthy and diseased hearts\",\"authors\":\"James A. Coleman , Julia Camps , Abdallah I. Hasaballa , Alfonso Bueno-Orovio\",\"doi\":\"10.1016/j.compbiomed.2025.111222\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Abnormal patterns of ventricular repolarisation are thought to contribute to lethal arrhythmias in various cardiac conditions, including inherited and acquired channelopathies, cardiomyopathies, and ischaemic heart disease. However, methods to detect these repolarisation abnormalities are limited.</div><div>In this study, we introduce and assess a novel simulation-based method to infer ventricular activation and repolarisation times from the 12-lead electrocardiogram (ECG) and magnetic resonance-derived ventricular anatomical reconstruction, applicable for the first time to both healthy controls and cases with abnormal repolarisation.</div><div>First, ventricular activation times were reconstructed through iterative refinement of early activation sites and conduction velocities, until the model and target QRS complexes matched. Then, ventricular repolarisation times were reconstructed through iterative refinement of ventricular action potential durations and an action potential shape parameter until the model and target T waves matched, including regularisation. Repolarisation inference was evaluated against 18 benchmark simulations with known repolarisation times, including both control and hypertrophic cardiomyopathy (HCM) cases with abnormal repolarisation.</div><div>Inferred repolarisation times showed good agreement with the ground truth in control and HCM (Spearman <span><math><mrow><mi>r</mi><mo>=</mo><mn>0.63</mn><mo>±</mo><mn>0.11</mn></mrow></math></span> and <span><math><mrow><mn>0.65</mn><mo>±</mo><mn>0.19</mn></mrow></math></span>, respectively), with the inferred model T waves closely matching the target T waves (<span><math><mrow><mi>r</mi><mo>=</mo><mn>0.81</mn><mo>±</mo><mn>0.05</mn></mrow></math></span> and <span><math><mrow><mn>0.78</mn><mo>±</mo><mn>0.08</mn></mrow></math></span>, respectively). The method further demonstrated flexibility in reconstructing the macroscopic patterns of delayed repolarisation across a range of abnormal ventricular repolarisation sequences, demonstrating applicability to a wide range of pathological scenarios.</div><div>Simulation-based inference can accurately reconstruct repolarisation times from the 12-lead ECG in cases with both normal and abnormal repolarisation patterns.</div></div>\",\"PeriodicalId\":10578,\"journal\":{\"name\":\"Computers in biology and medicine\",\"volume\":\"198 \",\"pages\":\"Article 111222\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2025-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Computers in biology and medicine\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0010482525015756\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computers in biology and medicine","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0010482525015756","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
Simulation-based digital twinning of activation and repolarisation sequences from the ECG across healthy and diseased hearts
Abnormal patterns of ventricular repolarisation are thought to contribute to lethal arrhythmias in various cardiac conditions, including inherited and acquired channelopathies, cardiomyopathies, and ischaemic heart disease. However, methods to detect these repolarisation abnormalities are limited.
In this study, we introduce and assess a novel simulation-based method to infer ventricular activation and repolarisation times from the 12-lead electrocardiogram (ECG) and magnetic resonance-derived ventricular anatomical reconstruction, applicable for the first time to both healthy controls and cases with abnormal repolarisation.
First, ventricular activation times were reconstructed through iterative refinement of early activation sites and conduction velocities, until the model and target QRS complexes matched. Then, ventricular repolarisation times were reconstructed through iterative refinement of ventricular action potential durations and an action potential shape parameter until the model and target T waves matched, including regularisation. Repolarisation inference was evaluated against 18 benchmark simulations with known repolarisation times, including both control and hypertrophic cardiomyopathy (HCM) cases with abnormal repolarisation.
Inferred repolarisation times showed good agreement with the ground truth in control and HCM (Spearman and , respectively), with the inferred model T waves closely matching the target T waves ( and , respectively). The method further demonstrated flexibility in reconstructing the macroscopic patterns of delayed repolarisation across a range of abnormal ventricular repolarisation sequences, demonstrating applicability to a wide range of pathological scenarios.
Simulation-based inference can accurately reconstruct repolarisation times from the 12-lead ECG in cases with both normal and abnormal repolarisation patterns.
期刊介绍:
Computers in Biology and Medicine is an international forum for sharing groundbreaking advancements in the use of computers in bioscience and medicine. This journal serves as a medium for communicating essential research, instruction, ideas, and information regarding the rapidly evolving field of computer applications in these domains. By encouraging the exchange of knowledge, we aim to facilitate progress and innovation in the utilization of computers in biology and medicine.