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Hypertrophic cardiomyopathy (HCM), including obstructive HCM and non-obstructive HCM, can lead to sudden cardiac arrest in adolescents and athletes. Early diagnosis and treatment through auscultation of different types of HCM can prevent the occurrence of malignant events. However, it is challenging to distinguish the pathological information of HCM related to differential left ventricular outflow tract pressure gradients. To address this issue, a classification method based on weighted bispectrum features of heart sounds (HSs) is proposed for efficient and cost-effective HCM analysis. Preprocessing is first applied to remove background noise during HS acquisition. Then, the bispectrum contour map is calculated, and 56-dimensional features are extracted to represent the pathological information of HCM. Next, an adaptive threshold weighting mutual information method is proposed for feature selection and weighted fusion. Finally, the CNN-RF classifier model is built to automatically identify different types of HCM cases. A clinical dataset of normal and two types of HCM HSs is utilized for validation. The results show that the proposed method performs well, with a classification accuracy reaching 94.4%. It provides a reliable reference for HCM diagnosis in young patients in clinical settings.
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http://dx.doi.org/10.1007/s13246-024-01506-w | DOI Listing |
Biomed Eng Lett
September 2025
Department of Cardiovascular Ultrasound, The First Hospital of China Medical University, Shenyang, China.
Abstract: Hypertrophic cardiomyopathy (HCM) is a common hereditary heart disease and is the leading cause of sudden cardiac death in adolescents. Septal hypertrophy (SH) and apical hypertrophy (AH) are two common types. The former is characterized by abnormal septal myocardial thickening and the latter by left ventricular apical hypertrophy, both of which significantly increase the risk of heart failure, arrhythmias, and other serious complications.
View Article and Find Full Text PDFAnal Chim Acta
October 2025
Center of Laboratory Medicine, Beijing, Key Laboratory for Molecular Diagnostics of Cardiovascular Diseases, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Diseases & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 1000
Background: The treatment and prognosis of cardiac amyloidosis (CA) depend heavily on the accurate identification of amyloid protein types. Histopathological methods are the most commonly used approach, but often produce inconclusive results. The application of mass spectrometry with laser microdissection mass spectrometry based on non-targeted proteomics in CA diagnosis is gradually being recognized, but it is expensive, time-consuming, and still in the early stages of scientific research applications.
View Article and Find Full Text PDFSci Rep
August 2025
Faculty of Heat and Refrigeration Engineering, Industrial University of Ho Chi Minh City (IUH), 12 Nguyen Van Bao, Hanh Thong ward, Ho Chi Minh City, Vietnam.
In current numerical work, a mathematical model for an air collector with latent heat storage is established and solved using the finite difference method. The glass, absorber plate, and air flow temperatures are described in one-dimensional unsteady terms. The storage material simulation is formed by a two-dimensional unsteady modeling and solved using the enthalpy method.
View Article and Find Full Text PDFInt J Microbiol
July 2025
Faculty of Applied Technology, School of Technology, Van Lang University, Ho Chi Minh City, Vietnam.
, an opportunistic pathogen, is responsible for a wide range of healthcare-associated infections (HAIs), particularly in patients in intensive care units (ICUs). Carbapenem-resistant (CRAB) is of particular concern due to its extensive multidrug resistance (MDR) and limited treatment options. In Vietnam, CRAB has become increasingly prevalent, with resistant mechanisms primarily attributed to the presence of and genes.
View Article and Find Full Text PDFCureus
June 2025
Cardiology, Heart of Melbourne, Melbourne, AUS.
Background Hypertrophic cardiomyopathy (HCM) is a genetic heart disease that poses a risk for sudden cardiac death. It has not been studied systematically in Southeast Asian countries. The purpose of this study was to investigate the characteristics and patterns of fibrosis in HCM, as well as to determine the risk of sudden cardiac death in relation to age, sex, and myocardial fibrosis in Brunei Darussalam.
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