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Large Animal Model for Evaluating the Efficacy of the Gene Therapy in Ischemic Heart
Published on: September 2, 2021
Heart failure: advances through genomics
Esther E Creemers1, Arthur A Wilde, Yigal M Pinto
1The Heart Failure Research Center, Room K2-120, Academic Medical Center (AMC), Meibergdreef 15, 1105AZ Amsterdam, The Netherlands.
Insights
Heart failure, a common and deadly disease, stems from various causes including gene mutations. Genetic research is uncovering its molecular roots to develop new treatments for specific heart failure types.
Area of Science:
- Genomics and Molecular Biology
- Cardiovascular Medicine
Background:
- Heart failure is a widespread and fatal condition.
- Common causes include myocardial infarction and hypertension.
- Rarely, heart failure can result from inherited single gene mutations.
Purpose of the Study:
- To explore the genetic and genomic underpinnings of heart failure.
- To identify novel diagnostic and therapeutic strategies for heart failure subtypes.
Main Methods:
- Application of comprehensive genetic and genomic approaches.
- Analysis of molecular mechanisms contributing to heart failure.
Main Results:
- Disentangling the diverse molecular basis of heart failure.
- Identifying genetic factors contributing to disease development.
Conclusions:
- Genetic and genomic studies are crucial for understanding heart failure.
- These approaches hold promise for developing targeted therapies for specific heart failure patient groups.
Abstract:
Heart failure is an increasingly prevalent and highly lethal disease that is most often caused by underlying pathologies, such as myocardial infarction or hypertension, but it can also be the result of a single gene mutation. Comprehensive genetic and genomic approaches are starting to disentangle the diverse molecular underpinnings of both forms of the disease and promise to yield much-needed novel diagnostic and therapeutic options for specific subtypes of heart failure.
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