# Towards fully automated synthetic ECV quantification: an open-access machine learning-based approach for fast blood draw-free CMR

**Authors:** Rebecca Elisabeth Beyer, Markus Hüllebrand, Patrick Doeblin, Ann Laube, Maximilian Leo Müller, Christian Stehning, Stefanie Maria Werhahn, Wensu Chen, Anja Hennemuth, Sebastian Kelle

PMC · DOI: 10.1038/s41598-026-43624-3 · 2026-03-10

## TL;DR

This paper introduces a fast, automated machine learning method to measure heart tissue fibrosis without needing blood samples, showing strong agreement with traditional methods.

## Contribution

A fully automated, blood-free machine learning approach for synthetic ECV quantification in CMR is developed and validated.

## Key findings

- Fully-automated synthetic ECV correlated strongly with conventional ECV (r = 0.79, p < 0.001).
- Bland–Altman analysis showed minimal mean difference of 0.4% with moderate limits of agreement.
- The method supports efficient and consistent assessment of myocardial fibrosis in research settings.

## Abstract

Extracellular volume (ECV) quantification involves time-consuming multi-step post-processing and a blood draw for hematocrit analysis. This study aimed to develop a fully automated blood draw-free, machine learning-based approach for synthetic ECV assessment for non-invasive assessment of diffuse myocardial fibrosis. We retrospectively evaluated a large clinical cohort of 1092 patients who underwent CMR and ECV measurement at 1.5T or 3T. Participants were divided into training (n = 767) and validation (n = 325) cohorts. Manual contouring of T1 maps was used to iteratively develop a neural network segmentation model, which was then applied for automated analysis. Fully-automated synthetic ECV was calculated using validated sex- and field strength-specific models. Agreement was assessed using Student’s t-test, Pearson correlation, Bland–Altman analysis, and classification analysis. Fully-automated synthetic ECV showed strong correlation with conventional ECV (r = 0.79, p < 0.001), with no significant differences (26.9% ± 4.9% vs. 27.3% ± 6.4%, p = 0.056). Bland–Altman analysis indicated minimal mean difference of 0.4% with moderate limits of agreement (LoA) spanning − 7.24% to + 8.07%, with good agreement for values of up to 35% (mean difference 0.1%, LoA: − 5.38% to + 5.23%). Fully automated synthetic ECV offers a blood-free proof-of-concept for large-scale post-processing, supporting consistent and efficient assessment of myocardial fibrosis in research settings, pending further validation for clinical use at higher ECV ranges.

The online version contains supplementary material available at 10.1038/s41598-026-43624-3.

## Full-text entities

- **Diseases:** anemia (MESH:D000740), amyloidosis (MESH:D000686), septal disease (MESH:D006343), diffuse (MESH:D008228), cardiac conditions (MESH:D006331), papillary muscle fibrosis (MESH:D002291), Myocardial fibrosis (MESH:D005355), mitral valve prolapse (MESH:D008945), arrhythmia (MESH:D001145), stroke (MESH:D020521)
- **Chemicals:** ECV (-), Gadobutrol (MESH:C090600), gadolinium (MESH:D005682)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12976349/full.md

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Source: https://tomesphere.com/paper/PMC12976349