Evidence map›Paper›PMID 42019569›Full record

ArticleJournal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance2026

Artificial-intelligence-based feature mapping of native oxygenation-sensitive cardiovascular magnetic resonance images for classifying cardiomyopathies.

Faezeh LotfiKazemi, Mitchel Benovoy, Michael Chetrit, Leila Haririsanati, Javad Rafiee, Judy M Luu, Matthias G Friedrich

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Article in Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Faezeh LotfiKazemiDepartment of Experimental Medicine, McGill University, Montreal, Quebec, Canada.
Mitchel BenovoyArea19 Medical Inc., Montreal, Quebec, Canada.
Michael ChetritDepartment of Medicine, McGill University, Montreal, Quebec, Canada.
Leila HaririsanatiResearch Institute, McGill University Health Centre, Montreal, Quebec, Canada.
Javad RafieeResearch Institute, McGill University Health Centre, Montreal, Quebec, Canada.
Judy M LuuDepartment of Experimental Medicine, McGill University, Montreal, Quebec, Canada; Department of Medicine, McGill University, Montreal, Quebec, Canada.
Matthias G FriedrichDepartment of Experimental Medicine, McGill University, Montreal, Quebec, Canada; Diagnostic Radiology, McGill University, Montreal, Quebec, Canada. Electronic address: matthias.friedrich@mcgill.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular magnetic resonance (CMR) is the non-invasive gold standard for myocardial tissue characterization. This, however, requires additional sequences and typically the use of contrast agents. Native oxygenation-sensitive cardiovascular magnetic resonance (OS-CMR) has been introduced for assessing coronary vascular function. The resulting images may allow for the extraction of tissue information. We hypothesized that deep learning can extract phenotype-specific information from OS-CMR images to enable contrast-free classification of myocardial pathology.

methodsWe developed and trained a deep learning algorithm to extract tissue information for classifying myocardial pathology.

methodsWe developed and trained a deep learning algorithm to extract tissue information for classifying myocardial pathology. We used data from 190 individuals classified as follows: Ischemic (n=42), non-ischemic (n=33), inflammation/edema (n=47), and healthy (n=68). We divided the scans into sets for training (70%), validation (20%), and testing (10%). The model was evaluated using a stratified five-fold cross-validation with Monte Carlo Dropout and residual learning. Beyond classification, the regions and extent of the layer activation maps were compared with results from blinded expert reads. Spatial agreement was quantified using Dice similarity coefficients.

resultsThe model achieved class-specific area under the curve (AUC) values of 0.93 for healthy myocardium, 0.80 for ischemic cardiomyopathy, 0.89 for non-ischemic cardiomyopathy, and 0.96 for inflammation/edema. Artificial intelligence-derived feature maps demonstrated spatial correspondence with expert-defined lesions (Dice values: 0.85 for transmural ischemia, 0.90 for subendocardial involvement, 0.83 and 0.93 for non-ischemic lesions in hypertrophic cardiomyopathy and dilated cardiomyopathy, and 0.93 for global edema).

conclusionOS-CMR images contain phenotype-specific information that can be extracted by deep learning to support a diagnostic classification of myocardial tissue pathology. The multi-parametric analysis may enable a comprehensive, ultra-efficient and needle-free CMR scan.

Indexed as

Deep learningFeature map visualizationMyocardial tissue characterizationOS-CMRVGG19

Identifiers

PMID42019569
PMCPMC13375919

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.