Precision Medicine in Cardiomyopathy: Advances and Future Directions
This review explores how precision medicine is transforming the diagnosis, classification, and treatment of cardiomyopathies. It focuses on the integration of genetic profiling, biomarkers, and imaging to deliver more tailored and effective care. We review major cardiomyopathy subtypes: hypertrophic, dilated, restrictive, and arrhythmogenic right ventricular, with a focus on genetic drivers, including mitochondrial mutations. Pediatric forms are discussed in the context of syndromic and non-syndromic differences. We highlight the clinical value of combining biomarkers (molecular and serological) with imaging modalities, such as echocardiography, for better risk stratification, especially in predicting sudden cardiac death. The utility of animal models in translating genetic findings into disease understanding is also emphasized. Finally, we touch on innovations like genome editing, gene therapies, and pharmacogenomics for personalized treatment. Precision medicine offers a promising future for cardiomyopathy care. By targeting the underlying causes and tailoring treatment to each patient's genetic and molecular profile, we can achieve more accurate diagnoses, better risk prediction, and improved outcomes, bringing us closer to truly individualized cardiovascular care.
Authors
- A Ansari (ORCID: https://orcid.org/0000-0001-6953-6119)
- Aliya Abbas Rizvi (ORCID: https://orcid.org/0000-0002-8039-7081)
- Mohammad Abbas (ORCID: https://orcid.org/0000-0002-2084-8856)
- Farzana Mahdi (ORCID: https://orcid.org/0000-0002-2188-2992)
- Bashir Ahmad Mir
- Shrikant Verma (ORCID: https://orcid.org/0000-0002-8356-8448)
- Sushma Verma
- Mahvish Mehdi
Institutions
- University of Lucknow (IN)
- Era's Lucknow Medical College and Hospital (IN)
Publication Details
- Journal
- Clinical Genetics
- Published
- 2025-09-21
- DOI
- https://doi.org/10.1111/cge.70072
- Citations
- 1
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.39