用于检测致心律失常性右室心肌病的人工智能增强心电图。

IF 3.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
European heart journal. Digital health Pub Date : 2023-12-09 eCollection Date: 2024-03-01 DOI:10.1093/ehjdh/ztad078
Ikram U Haq, Kan Liu, John R Giudicessi, Konstantinos C Siontis, Samuel J Asirvatham, Zachi I Attia, Michael J Ackerman, Paul A Friedman, Ammar M Killu
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引用次数: 0

摘要

目的:心电图异常通常是致心律失常性右室心肌病(ARVC)的首发症状,我们假设人工智能(AI)增强型心电图可以帮助识别ARVC患者,并作为一种有价值的疾病检测工具:我们创建了一个卷积神经网络,利用 12 导联心电图检测 ARVC。我们纳入了所有符合 2010 年特别工作组标准且具有致病基因变异的 ARVC 患者。所有病例心电图按 8:1:1 的比例随机分配到训练组、验证组和测试组。病例心电图与本机构的对照心电图按 1:100 的比例进行了年龄和性别匹配。共纳入 77 名患者(51% 为男性;平均年龄为 47.2 ± 19.9),包括 56 名 PKP2 患者、7 名 DSG2 患者、6 名 DSC2 患者、6 名 DSP 患者和 2 名 JUP 患者。使用 61 份病例心电图和 5009 份对照心电图对模型进行了训练;使用 7 份病例心电图和 678 份对照心电图对模型进行了验证,并使用 22 份病例心电图和 1256 份对照心电图对模型进行了测试。该模型的灵敏度、特异性、阳性预测值和阴性预测值分别为 77.3%、62.9%、3.32% 和 99.4%。心律心电图和中位搏动心电图的曲线下面积分别为 0.75 和 0.76:我们的研究发现,该模型在排除 ARVC 方面表现良好,并支持这样的概念,即如果有更多的队列可供网络训练,人工智能心电图可作为 ARVC 的生物标志物。下一步将进行多中心研究,包括其他中心的 ARVC 患者,以完善、测试和验证该算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial intelligence-enhanced electrocardiogram for arrhythmogenic right ventricular cardiomyopathy detection.

Aims: ECG abnormalities are often the first signs of arrhythmogenic right ventricular cardiomyopathy (ARVC) and we hypothesized that an artificial intelligence (AI)-enhanced ECG could help identify patients with ARVC and serve as a valuable disease-detection tool.

Methods and results: We created a convolutional neural network to detect ARVC using a 12-lead ECG. All patients with ARVC who met the 2010 task force criteria and had disease-causative genetic variants were included. All case ECGs were randomly assigned in an 8:1:1 ratio into training, validation, and testing groups. The case ECGs were age- and sex-matched with control ECGs at our institution in a 1:100 ratio. Seventy-seven patients (51% male; mean age 47.2 ± 19.9), including 56 patients with PKP2, 7 with DSG2, 6 with DSC2, 6 with DSP, and 2 with JUP were included. The model was trained using 61 case ECGs and 5009 control ECGs; validated with 7 case ECGs and 678 control ECGs and tested in 22 case ECGs and 1256 control ECGs. The sensitivity, specificity, positive and negative predictive values of the model were 77.3, 62.9, 3.32, and 99.4%, respectively. The area under the curve for rhythm ECG and median beat ECG was 0.75 and 0.76, respectively.

Conclusion: Our study found that the model performed well in excluding ARVC and supports the concept that the AI ECG can serve as a biomarker for ARVC if a larger cohort were available for network training. A multicentre study including patients with ARVC from other centres would be the next step in refining, testing, and validating this algorithm.

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