arXiv:2601.01176cs.CV2026-01

用超声心动图视频同时诊断和预测心衰病因,突破传统二分类局限。

CardioMOD-Net: A Modal Decomposition-Neural Network Framework for Diagnosis and Prognosis of HFpEF from Echocardiography Cine Loops

  • 通过高阶动态模态分解提取视频时序特征,融合视觉变压器实现多类诊断
  • 对小鼠模型的四种病因分型准确率达65%,预测发病时间误差仅21.72周
  • 首次从单个超声视频完成病因分型与发病时间连续预测,适合预临床研究

心力衰竭伴射血分数保留(HFpEF)由多种共病引发,进展缓慢且早期难以诊断。现有基于超声心动图的人工智能模型主要聚焦于人类的二分类检测,无法提供特定共病表型或疾病恶化前的时间预测。本文提出统一的AI框架CardioMOD-Net,直接从标准超声心动图电影片段中实现多类别诊断与连续发病时间预测。研究使用四组小鼠数据:对照组(CTL)、高血糖(HG)、肥胖(OB)和系统性动脉高血压(SAH)。采用二维胸骨旁长轴电影片段,通过高阶动态模态分解(HODMD)提取时序特征,输入共享潜在表示的视觉变压器,分别用于分类诊断与回归预测发病年龄。整体诊断准确率为65%,所有类别均超过50%;误判主要出现在早期阶段的OB或SAH与对照组之间。预后模块的均方根误差为21.72周,其中OB和SAH组预测最准,预测发病时间与真实分布高度吻合。该框架证明,在小样本条件下,仅凭单个电影片段即可实现多类表型分型与发病时间连续预测,为预临床研究中的诊断与预后整合建模提供了基础。

原文摘要 · Abstract (English)

Introduction: Heart failure with preserved ejection fraction (HFpEF) arises from diverse comorbidities and progresses through prolonged subclinical stages, making early diagnosis and prognosis difficult. Current echocardiography-based Artificial Intelligence (AI) models focus primarily on binary HFpEF detection in humans and do not provide comorbidity-specific phenotyping or temporal estimates of disease progression towards decompensation. We aimed to develop a unified AI framework, CardioMOD-Net, to perform multiclass diagnosis and continuous prediction of HFpEF onset directly from standard echocardiography cine loops in preclinical models. Methods: Mouse echocardiography videos from four groups were used: control (CTL), hyperglycaemic (HG), obesity (OB), and systemic arterial hypertension (SAH). Two-dimensional parasternal long-axis cine loops were decomposed using Higher Order Dynamic Mode Decomposition (HODMD) to extract temporal features for downstream analysis. A shared latent representation supported Vision Transformers, one for a classifier for diagnosis and another for a regression module for predicting the age at HFpEF onset. Results: Overall diagnostic accuracy across the four groups was 65%, with all classes exceeding 50% accuracy. Misclassifications primarily reflected early-stage overlap between OB or SAH and CTL. The prognostic module achieved a root-mean-square error of 21.72 weeks for time-to-HFpEF prediction, with OB and SAH showing the most accurate estimates. Predicted HFpEF onset closely matched true distributions in all groups. Discussion: This unified framework demonstrates that multiclass phenotyping and continuous HFpEF onset prediction can be obtained from a single cine loop, even under small-data conditions. The approach offers a foundation for integrating diagnostic and prognostic modelling in preclinical HFpEF research.

心衰预测超声影像多任务学习预临床研究

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