This Collection aims to address various aspects of hypertrophic cardiomyopathy. The recent introduction of cardiac myosin inhibitors has opened a new horizon for the management of hypertrophic cardiomyopathy. In light of this development, it is timely to review key issues surrounding hypertrophic cardiomyopathy, including heart failure, sudden cardiac death, arrhythmias such as atrial fibrillation, thromboembolic events like ischemic stroke, and genetics. We look forward to receiving cutting-edge research and review articles that explore these issues. We also welcome submissions that utilize new techniques, such as artificial intelligence or state-of-the-art echocardiographic or cardiac magnetic resonance imaging technologies, to enhance diagnostic accuracy and improve patient outcomes.
It aims to address a wide range of topics, including but not limited to:
- Evaluation of sudden cardiac death in hypertrophic cardiomyopathy
- Evaluation of heart failure risk in hypertrophic cardiomyopathy
- Evaluation of arrhythmias, including atrial fibrillation, in hypertrophic cardiomyopathy
- Evaluation of thromboembolic risk in hypertrophic cardiomyopathy
- Evaluation of prognosis in hypertrophic cardiomyopathy
- Echocardiography and/or cardiac magnetic resonance imaging in the evaluation of hypertrophic cardiomyopathy
- Applications of machine learning and deep learning approaches for better prediction of prognosis in hypertrophic cardiomyopathy
- Genetics in hypertrophic cardiomyopathy
- Exercise in hypertrophic cardiomyopathy
- Clinical trials, translational, or animal research studies in hypertrophic cardiomyopathy
All submissions will undergo peer review, which will be completed within 4 weeks as part of the Expedited Review process.
JCVI welcomes manuscripts that contribute to enhancing and widening our understanding of hypertrophic cardiomyopathy.