利用机器学习在英国生物银行成像研究中预测12导联心电图左心室肥厚。

IF 3.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS European heart journal. Digital health Pub Date : 2023-08-01 DOI:10.1093/ehjdh/ztad037
Hafiz Naderi, Julia Ramírez, Stefan van Duijvenboden, Esmeralda Ruiz Pujadas, Nay Aung, Lin Wang, Choudhary Anwar Ahmed Chahal, Karim Lekadir, Steffen E Petersen, Patricia B Munroe
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摘要

目的:左心室肥厚(LVH)是一种确定的、独立的心血管疾病预测指标。从心电图(ECG)得出的指标已被用于推断LVH的存在,但灵敏度有限。本研究旨在使用12导联心电图对心血管磁共振(CMR)成像定义的LVH进行分类,以实现成本效益高的患者分层。方法和结果:我们从英国生物银行成像研究中37534名参与者的12导联心电图中提取了与LVH已知生理关联的ECG生物标志物。采用logistic回归、支持向量机(SVM)和随机森林(RF)等方法建立ECG生物标志物与临床变量的分类模型。数据集被分成80%的训练集和20%的测试集进行性能评估。采用十倍交叉验证,并通过分离基于UK Biobank成像中心的数据进行进一步的验证测试。QRS振幅和血压(P < 0.001)是与LVH最密切相关的特征。logistic回归分类准确率为81%[灵敏度70%,特异度81%,受试者操作曲线下面积(AUC) 0.86], SVM准确率81%(灵敏度72%,特异度81%,AUC 0.85), RF准确率72%(灵敏度74%,特异度72%,AUC 0.83)。与单独使用临床变量相比,ECG生物标志物增强了所有分类器的模型性能。英国生物银行成像中心的验证测试证明了我们模型的稳健性。结论:结合ECG生物标志物和临床变量能够预测CMR定义的LVH。我们的研究结果支持心电图作为一种廉价的筛查工具,对LVH患者进行风险分层,作为进一步影像学检查的前奏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Predicting left ventricular hypertrophy from the 12-lead electrocardiogram in the UK Biobank imaging study using machine learning.

Aims: Left ventricular hypertrophy (LVH) is an established, independent predictor of cardiovascular disease. Indices derived from the electrocardiogram (ECG) have been used to infer the presence of LVH with limited sensitivity. This study aimed to classify LVH defined by cardiovascular magnetic resonance (CMR) imaging using the 12-lead ECG for cost-effective patient stratification.

Methods and results: We extracted ECG biomarkers with a known physiological association with LVH from the 12-lead ECG of 37 534 participants in the UK Biobank imaging study. Classification models integrating ECG biomarkers and clinical variables were built using logistic regression, support vector machine (SVM) and random forest (RF). The dataset was split into 80% training and 20% test sets for performance evaluation. Ten-fold cross validation was applied with further validation testing performed by separating data based on UK Biobank imaging centres. QRS amplitude and blood pressure (P < 0.001) were the features most strongly associated with LVH. Classification with logistic regression had an accuracy of 81% [sensitivity 70%, specificity 81%, Area under the receiver operator curve (AUC) 0.86], SVM 81% accuracy (sensitivity 72%, specificity 81%, AUC 0.85) and RF 72% accuracy (sensitivity 74%, specificity 72%, AUC 0.83). ECG biomarkers enhanced model performance of all classifiers, compared to using clinical variables alone. Validation testing by UK Biobank imaging centres demonstrated robustness of our models.

Conclusion: A combination of ECG biomarkers and clinical variables were able to predict LVH defined by CMR. Our findings provide support for the ECG as an inexpensive screening tool to risk stratify patients with LVH as a prelude to advanced imaging.

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