利用人工智能心电图和超声心动图追踪转甲状腺素淀粉样变性心肌病的临床前期进展

Evangelos K Oikonomou, Veer Sangha, Sumukh Vasisht Shankar, Andreas Coppi, Harlan Krumholz, Khurram Nasir, Edward J Miller, Cesia Gallegos-Kattan, Sadeer G. Al-Kindi, Rohan Khera
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引用次数: 0

摘要

背景和目的:诊断转甲状腺素淀粉样变性心肌病(ATTR-CM)需要先进的成像技术,因此无法对临床前疾病进行大规模检测。我们研究了将人工智能(AI)应用于超声心动图(TTE)和心电图(ECG)作为量化 ATTR-CM 临床前趋势的可扩展策略。方法:在耶鲁-纽黑文健康系统(YNHHS)的年龄/性别匹配病例对照数据集上,我们训练了深度学习模型,以识别 TTE 视频和心电图图像上的 ATTR-CM 特异性特征(曲线下面积分别为 0.93 和 0.91)。我们在 YNHHS 的独立人群和休斯顿卫理公会医院(HMH)的外部人群中转诊进行心脏核淀粉样蛋白成像的所有研究中部署了这些模型,以使用年龄/性别调整线性混合模型定义 ATTR-CM 的 AI 定义概率的纵向趋势,并描述早期临床前阶段的分辨指标。结果:在云南新华医院(中位年龄 74 岁,44.3% 为女性)和哈医大一院(中位年龄 69 岁,34.5% 为女性)转诊的 984 名心脏核淀粉样蛋白成像患者中,分别有 112 人(11.4%)和 174 人(21.6%)检测出 ATTR-CM 阳性。在两个队列和两种模式中,从 7,423 张 TTE 和 32,205 张心电图得出的 AI 定义的 ATTR-CM 概率显示,病例与对照组相比,临床诊断前几年的进展速度明显更快(时间 x 组间交互作用 p ≤0.004)。在心脏核淀粉样蛋白成像前的一至三年窗口期,AI-Echo 的敏感性/特异性指标估计为 86.2%/44.2% [YNHHS] vs 65.7%/65.5% [HMH],AI-ECG 的敏感性/特异性指标估计为 89.8%/40.6% [YNHHS] vs 88.5%/35.1% [HMH]。结论:我们证明,针对超声心动图视频和心电图图像的人工智能工具能够对临床前 ATTR-CM 进行可扩展的识别,并标记出可能从风险调整疗法中获益的个体。
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Tracking the pre-clinical progression of transthyretin amyloid cardiomyopathy using artificial intelligence-enabled electrocardiography and echocardiography
Background and Aims: Diagnosing transthyretin amyloid cardiomyopathy (ATTR-CM) requires advanced imaging, precluding large-scale testing for pre-clinical disease. We examined the application of artificial intelligence (AI) to echocardiography (TTE) and electrocardiography (ECG) as a scalable strategy to quantify pre-clinical trends in ATTR-CM. Methods: Across age/sex-matched case-control datasets in the Yale-New Haven Health System (YNHHS) we trained deep learning models to identify ATTR-CM-specific signatures on TTE videos and ECG images (area under the curve of 0.93 and 0.91, respectively). We deployed these across all studies of individuals referred for cardiac nuclear amyloid imaging in an independent population at YNHHS and an external population from the Houston Methodist Hospitals (HMH) to define longitudinal trends in AI-defined probabilities for ATTR-CM using age/sex-adjusted linear mixed models, and describe discrimination metrics during the early pre-clinical stage. Results: Among 984 participants referred for cardiac nuclear amyloid imaging at YNHHS (median age 74 years, 44.3% female) and 806 at HMH (69 years, 34.5% female), 112 (11.4%) and 174 (21.6%) tested positive for ATTR-CM, respectively. Across both cohorts and modalities, AI-defined ATTR-CM probabilities derived from 7,423 TTEs and 32,205 ECGs showed significantly faster progression rates in the years before clinical diagnosis in cases versus controls (p for time x group interaction ≤0.004). In the one-to-three-year window before cardiac nuclear amyloid imaging sensitivity/specificity metrics were estimated at 86.2%/44.2% [YNHHS] vs 65.7%/65.5% [HMH] for AI-Echo, and 89.8%/40.6% [YNHHS] vs 88.5%/35.1% [HMH] for AI-ECG. Conclusions: We demonstrate that AI tools for echocardiographic videos and ECG images can enable scalable identification of pre-clinical ATTR-CM, flagging individuals who may benefit from risk-modifying therapies.
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