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Machine learning model detects cardiac amyloidosis on bone scintigraphy with high accuracy

Machine learning model detects cardiac amyloidosis on bone scintigraphy with high accuracy
Photo by Steve A Johnson / Unsplash
Key Takeaway
Consider the Amylo-Detect model as a potential screening tool for cardiac amyloidosis, but await prospective validation.

This development and validation study evaluated the Amylo-Detect machine learning model for predicting cardiac amyloidosis (CA)-suggestive uptake (Perugini grade >=2) on bone scintigraphy. The study included 11,616 consecutive all-comer patients referred for bone scintigraphy at Vienna General Hospital (2010-2023) and University Hospital Essen. The model was compared with existing scoring systems and clinical routine.

High-grade uptake prevalence was 3.0% (388 of 11,616 patients). Model performance showed an AUC of 0.93 in the development cohort, 0.91 in internal validation, and 0.91 in external validation. Notably, Amylo-Detect identified 12 of 42 patients (29%) with CA-suggestive uptake who were missed in clinical routine.

Safety and tolerability were not reported. Limitations were not reported in the input. The model is available as a web app for further evaluation.

Clinicians should interpret these results cautiously, as the study is observational and external validation is limited. The model may help reduce missed diagnoses, but prospective clinical utility studies are needed.

Study Details

Study typeCohort
Sample sizen = 11,616
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
Background Timely detection is crucial to improve outcomes in patients with cardiac amyloidosis (CA) by initiation of life-saving treatments. Although confirmatory bone scintigraphy is highly accurate for CA detection, identifying at-risk patients for referral remains challenging. Objectives This study aimed to develop and validate a machine learning model, Amylo-Detect, using structured multimodal electronic health record (EHR) data to guide referrals for confirmatory scintigraphy and monoclonal protein testing. Methods Consecutive all-comer patients (n=11,616) referred for bone scintigraphy at the Vienna General Hospital (2010-2023) were retrospectively included. Patients referred before August 2020 formed the development cohort. The remaining patients comprised the internal validation cohort. External validation was performed at the University Hospital Essen (n=1,521). Amylo-Detect was trained using 50 routinely available parameters to predict CA-suggestive uptake (Perugini grade >=2) and compared with an existing score and clinical routine. Results High-grade uptake was present in 388 patients (3.0%). Amylo-Detect demonstrated excellent performance in development (AUC 0.93), independent internal validation (AUC 0.91), and external validation cohort (AUC 0.91), outperforming existing scoring systems and clinical routine. Results were consistent across subgroups, even when crucial predictors were missing. Of the 42/388 (10.8%) patients missed in clinical routine, 12/42 (29%) were additionally detected by Amylo-Detect. The model further conveyed significant prognostic value for mortality and heart failure hospitalization. Conclusions We present Amylo-Detect, a validated EHR-based tool for CA risk prediction, available as a web app, allowing application and further evaluation. By improving timely detection and referral, Amylo-Detect promises to address diagnostic delays and improve outcomes.
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