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The potential of optical pumped magnetometer magnetocardiography (OPM-MCG) for diagnosing coronary artery disease (CAD) has been initially shown, yet lacks large-scale prospective research.Using invasive coronary angiography (ICA) as a reference, we constructed three feature sets for the development of machine learning (ML) models: a 'Heart' feature set consisting only of OPM-MCG features, a 'Clinical' feature set, and a 'Heart + Clinical' combined feature set. We assessed the performance of 11 ML models with 10-fold cross-validation and conducted a feature importance analysis.. Among 1513 participants (mean age 58.2 ± 12.0 years, 75.5% male), 1194 (78.92%) tested positive for ICA. Significant differences were observed in 'Heart' and 'Clinical' features between ICA-positive and negative groups. ML models using only 'Heart' features (AUC 0.84-0.88) outperformed those using only 'Clinical' features (AUC 0.62-0.75). Combining both feature types improved diagnostic accuracy (AUC 0.75-0.90). Feature importance analysis highlighted that 'Significant change of Ar-PN' in OPM-MCG was key for ICA diagnosis (47.8%), along with 'Abnormal Sp-TT', 'Significant change of Ps-PN', and 'Abnormal Mg-TT'. OPM-MCG has high performance in diagnosing CAD, and the significant change of Ar-PN is the most important feature. Cat Boost and random forest are more suitable for OPM-MCG to build ML diagnostic models for CAD.
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http://dx.doi.org/10.1088/1361-6579/adf0be | DOI Listing |
Microbiol Spectr
September 2025
Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil.
is a commensal bacterium that colonizes the gut of humans and animals and is a major opportunistic pathogen, known for causing multidrug-resistant healthcare-associated infections (HAIs). Its ability to thrive in diverse environments and disseminate antimicrobial resistance genes (ARGs) across ecological niches highlights the importance of understanding its ecological, evolutionary, and epidemiological dynamics. The CRISPR2 locus has been used as a valuable marker for assessing clonality and phylogenetic relationships in .
View Article and Find Full Text PDFClin Exp Immunol
September 2025
Orthopedic Center, Sunshine Union Hospital, High-tech Zone, Weifang City, Shandong Province, China.
Introduction: We attempted to perform a comprehensive bioinformatics analyses on osteoarthritis (OA) based on the NKT-related genes and explore the clinical related critical genes.
Methods: Differentially expressed genes (DEGs) and NKT-related genes from WGCNA were obtained using the dataset GSE114007, followed by intersection analysis to obtain NKT-related DEGs. Lasso regression, support vector machine and random forest were performed to screen feature genes, followed by verification with ROC curve, and nomogram model.
Front Mol Biosci
August 2025
Department of Rheumatology and Immunology, Mianyang Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Mianyang, Sichuan, China.
Background: The clinical differentiation between obstetric antiphospholipid syndrome (OAPS) and undifferentiated connective tissue disease (UCTD) presents significant diagnostic challenges. This study employs metabolomics to investigate metabolic reprogramming patterns in OAPS and UCTD, aiming to identify potential biomarkers for early diagnosis.
Methods: Using LC-MS-based metabolomics, we analyzed serum profiles from 40 OAPS patients (B1), 30 OAPS + UCTD patients (B2), 27 UCTD patients (B3), and 30 healthy controls (A1).
Front Microbiol
August 2025
BIOASTER, Lyon, France.
We propose an innovative technology to classify the Mechanism of Action (MoA) of antimicrobials and predict their novelty, called HoloMoA. Our rapid, robust, affordable and versatile tool is based on the combination of time-lapse Digital Inline Holographic Microscopy (DIHM) and Deep Learning (DL). In combination with hologram reconstruction.
View Article and Find Full Text PDFFront Toxicol
August 2025
Ncardia Services B.V., Leiden, Netherlands.
Introduction: Efficient preclinical prediction of cardiovascular side effects poses a pivotal challenge for the pharmaceutical industry. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are becoming increasingly important in this field due to inaccessibility of human native cardiac tissue. Current preclinical hiPSC-CMs models focus on functional changes such as electrophysiological abnormalities, however other parameters, such as structural toxicity, remain less understood.
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