<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(11)</volume><submitter>Eckstein J</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>This study challenges state-of-the-art cardiac amyloidosis (CA) diagnostics by feeding multi-chamber strain and cardiac function into supervised machine (SVM) learning algorithms.&lt;h4>Methods&lt;/h4>Forty-three CA (32 males; 79 years (IQR 71; 85)), 20 patients with hypertrophic cardiomyopathy (HCM, 10 males; 63.9 years (±7.4)) and 44 healthy controls (CTRL, 23 males; 56.3 years (IQR 52.5; 62.9)) received cardiovascular magnetic resonance imaging. Left atrial, right atrial and right ventricular strain parameters and cardiac function generated a 41-feature matrix for decision tree (DT), k-nearest neighbor (KNN), SVM linear and SVM radial basis function (RBF) kernel algorithm processing. A 10-feature principal component analysis (PCA) was conducted using SVM linear and RBF.&lt;h4>Results&lt;/h4>Forty-one features resulted in diagnostic accuracies of 87.9% (AUC = 0.960) for SVM linear, 90.9% (0.996; Precision = 94%; Sensitivity = 100%; F1-Score = 97%) using RBF kernel, 84.9% (0.970) for KNN, and 78.8% (0.787) for DT. The 10-feature PCA achieved 78.9% (0.962) via linear SVM and 81.8% (0.996) via RBF SVM. Explained variance presented bi-atrial longitudinal strain and left and right atrial ejection fraction as valuable CA predictors.&lt;h4>Conclusion&lt;/h4>SVM RBF kernel achieved competitive diagnostic accuracies under supervised conditions. Machine learning of multi-chamber cardiac strain and function may offer novel perspectives for non-contrast clinical decision-support systems in CA diagnostics.</pubmed_abstract><journal>Diagnostics (Basel, Switzerland)</journal><pagination>2693</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9689404</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Machine Learning Challenge: Detection of Cardiac Amyloidosis Based on Bi-Atrial and Right Ventricular Strain and Cardiac Function.</pubmed_title><pmcid>PMC9689404</pmcid><pubmed_authors>Piran M</pubmed_authors><pubmed_authors>Sciacca V</pubmed_authors><pubmed_authors>Weise Valdes E</pubmed_authors><pubmed_authors>Eckstein J</pubmed_authors><pubmed_authors>Paluszkiewicz L</pubmed_authors><pubmed_authors>Burchert W</pubmed_authors><pubmed_authors>Moghadasi N</pubmed_authors><pubmed_authors>Korperich H</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Machine Learning Challenge: Detection of Cardiac Amyloidosis Based on Bi-Atrial and Right Ventricular Strain and Cardiac Function.</name><description>&lt;h4>Background&lt;/h4>This study challenges state-of-the-art cardiac amyloidosis (CA) diagnostics by feeding multi-chamber strain and cardiac function into supervised machine (SVM) learning algorithms.&lt;h4>Methods&lt;/h4>Forty-three CA (32 males; 79 years (IQR 71; 85)), 20 patients with hypertrophic cardiomyopathy (HCM, 10 males; 63.9 years (±7.4)) and 44 healthy controls (CTRL, 23 males; 56.3 years (IQR 52.5; 62.9)) received cardiovascular magnetic resonance imaging. Left atrial, right atrial and right ventricular strain parameters and cardiac function generated a 41-feature matrix for decision tree (DT), k-nearest neighbor (KNN), SVM linear and SVM radial basis function (RBF) kernel algorithm processing. A 10-feature principal component analysis (PCA) was conducted using SVM linear and RBF.&lt;h4>Results&lt;/h4>Forty-one features resulted in diagnostic accuracies of 87.9% (AUC = 0.960) for SVM linear, 90.9% (0.996; Precision = 94%; Sensitivity = 100%; F1-Score = 97%) using RBF kernel, 84.9% (0.970) for KNN, and 78.8% (0.787) for DT. The 10-feature PCA achieved 78.9% (0.962) via linear SVM and 81.8% (0.996) via RBF SVM. Explained variance presented bi-atrial longitudinal strain and left and right atrial ejection fraction as valuable CA predictors.&lt;h4>Conclusion&lt;/h4>SVM RBF kernel achieved competitive diagnostic accuracies under supervised conditions. Machine learning of multi-chamber cardiac strain and function may offer novel perspectives for non-contrast clinical decision-support systems in CA diagnostics.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-05T10:57:05.96Z</modification><creation>2025-04-05T10:57:05.96Z</creation></dates><accession>S-EPMC9689404</accession><cross_references><pubmed>36359536</pubmed><doi>10.3390/diagnostics12112693</doi></cross_references></HashMap>