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Genetics and pharmacogenetics in heart failure.
Eric M Snyder1, Thomas P Olson, Bruce D Johnson
1Division of Cardiovascular Diseases, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA. snyder.eric@mayo.edu
Genetic factors significantly influence heart failure development and treatment response. Understanding these genetic variations can personalize pharmacologic interventions for better patient outcomes in heart failure.
Area of Science:
- Cardiology
- Genetics
- Pharmacology
Background:
- Heart failure (HF) is a complex, heterogeneous disease influenced by genetic and environmental factors.
- While some HF forms are clearly heritable, the genetic role in classic HF pathogenesis requires further elucidation.
- Modifier genes impact HF patient exercise capacity, organ function, and survival.
Purpose of the Study:
- To review the role of genetic variations in heart failure.
- To explore the influence of modifier genes on HF pathophysiology and treatment.
- To highlight the impact of genetics on pharmacologic intervention in HF.
Main Methods:
- Literature review focusing on genetic modifiers in heart failure.
- Analysis of studies investigating gene-environment interactions in HF.
- Examination of genetic influences on adrenergic, renin-angiotensin-aldosterone, and vascular systems in HF.
Main Results:
- Genetic variations play a crucial role in HF development and progression.
- Specific genes modulate exercise capacity, cardiovascular function, and survival in HF patients.
- Genetic factors influence individual responses to heart failure pharmacotherapies.
Conclusions:
- Genetics significantly impacts heart failure heterogeneity and progression.
- Identifying genetic profiles can optimize pharmacologic treatments for heart failure.
- Personalized medicine approaches in heart failure require understanding genetic determinants.
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