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Biosignal Fingerprinting: A Cross-Modal PPG-ECG Foundation Model

arXiv:2605.0957959.9
Predicted impact top 37% in LG · last 90 daysOriginality Highly original
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For cardiovascular monitoring, this provides a modality-agnostic, privacy-preserving representation that works with single-modality input, enabling scalable wearable-based cardiac assessment.

The authors introduce biosignal fingerprints from a cross-modal PPG-ECG foundation model (M2AE) trained on 3.4M paired signals, achieving competitive or superior performance on 7 downstream tasks including CVD classification (AUROC 0.974) and hypertension detection (AUROC 0.877), with up to 27.7% improvement over specialist models.

Cardiovascular disease remains the leading cause of global mortality, yet scalable cardiac monitoring is hindered by the gap between diagnostic-rich ECG and ubiquitous wearable PPG. Bridging this gap requires representations that are compact, transferable across modalities and devices, and deployable without task-specific retraining. Here we introduce biosignal fingerprints: compact latent representations of cardiovascular state derived from a cross-modal foundation model, the Multi-modal Masked Autoencoder (M2AE), trained on over 3.4 million paired ECG and PPG signals. M2AE integrates modality-specific encoders with a shared bottleneck and dual decoders, jointly optimized using reconstruction and cross-modal contrastive objectives, yielding generalizable fingerprints that retain intra- and inter-modality features. Like a biometric fingerprint, these representations uniquely encode an individual's cardiovascular state in a modality-agnostic, privacy-preserving form reusable across clinical tasks without exposing raw waveform data or requiring model retraining. Across 7 downstream tasks, spanning cross-modal reconstruction, cardiovascular disease classification, hypertension detection, mortality prediction, and demographic inference, biosignal fingerprints achieve competitive or superior performance compared to leading domain-specialist foundation models in frozen settings, including an AUROC of 0.974 for five-class CVD classification and 0.877 for hypertension detection, with a maximum improvement of 27.7% in AUROC across 5 classification tasks. Critically, strong performance is maintained with only a single modality, enabling deployment in resource-constrained, single-sensor environments typical of real-world wearable monitoring, with direct implications for continuous cardiovascular monitoring across clinical and consumer health settings.

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