Author ORCID Identifier
https://orcid.ord/0009-0000-4100-6271
Abstract
Subclinical myocardial disease refers to pathological cardiac changes that precede overt symptoms. It represents an emerging frontier in cardiovascular disease prevention; wherein early detection of myocardial dysfunction could allow timely intervention to avert heart failure (HF) and other outcomes. This narrative review summarizes the current and emerging tools for detecting subclinical myocardial disease, including advanced cardiac imaging and circulating biomarkers, and discusses their potential to improve risk stratification and preventive care in asymptomatic high-risk individuals. Novel echocardiographic measures such as global longitudinal strain (GLS) can unmask subtle systolic dysfunction despite preserved ejection fraction, while cardiac magnetic resonance (CMR) tissue mapping (T1 mapping and extracellular volume [ECV] fraction) enables quantification of diffuse myocardial fibrosis. Circulating biomarkers of cardiomyocyte injury and hemodynamic stress, namely high-sensitivity cardiac troponins and natriuretic peptides, offer quantitative indices of subclinical myocardial damage and wall stress that correlate with future HF risk. Positron emission tomography (PET) imaging provides sensitive detection of myocardial inflammation and microvascular dysfunction. We highlight how integrating these modalities can identify high-risk patients in the pre-HF stage (ACC/AHA Stage B), defined by structural or functional cardiac abnormalities without symptoms, allowing initiation of preventive therapies.
Publication Date
2025
Publisher
JSS Academy of Higher Education & Research
Conflict of Interest
none
Keywords
Myocardial Diseases, Ventricular Dysfunction, Echocardiography, Magnetic Resonance Imaging, Natriuretic Peptides
Word Count
2813
Recommended Citation
Darpan Sheth P, S. C, Rehman N.
Subclinical Myocardial Disease: The Next Frontier in Cardiovascular Prevention..
Digital Journal of Clinical Medicine.
2025;
8(1):
-.
doi:
https://doi.org/10.55691/2582-3868.1289
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Comments
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