利用机器学习从英国生物库成像研究的 12 导联心电图预测左心室肥厚。

IF 3.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
European heart journal. Digital health Pub Date : 2023-06-01 eCollection 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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引用次数: 0

摘要

目的:左心室肥厚(LVH)是心血管疾病的公认独立预测指标。由心电图(ECG)得出的指标被用于推断是否存在左心室肥厚,但灵敏度有限。本研究旨在利用 12 导联心电图对心血管磁共振(CMR)成像确定的 LVH 进行分类,以便对患者进行经济有效的分层:我们从英国生物库成像研究的 37 534 名参与者的 12 导联心电图中提取了与 LVH 有已知生理关联的心电图生物标志物。我们使用逻辑回归、支持向量机(SVM)和随机森林(RF)建立了整合心电图生物标志物和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,用于性能评估。应用了十倍交叉验证,并根据英国生物库成像中心的数据进行了进一步的验证测试。QRS 波幅和血压(P < 0.001)是与 LVH 关系最密切的特征。逻辑回归分类的准确率为 81% [灵敏度 70%,特异性 81%,接收者运算曲线下面积 (AUC) 0.86],SVM 的准确率为 81%(灵敏度 72%,特异性 81%,AUC 0.85),RF 的准确率为 72%(灵敏度 74%,特异性 72%,AUC 0.83)。与单独使用临床变量相比,心电图生物标志物提高了所有分类器的模型性能。英国生物库成像中心的验证测试证明了我们模型的稳健性:结论:心电图生物标志物和临床变量的组合能够预测 CMR 定义的 LVH。我们的研究结果支持将心电图作为一种廉价的筛查工具,用于对 LVH 患者进行风险分层,作为高级成像的前奏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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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