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Published on: October 3, 2019
Clonal hematopoiesis of indeterminate potential and cardiovascular diseases: A review
Nagendra Boopathy Senguttuvan1, Vinodhini Subramanian2, Muralidharan Tr3
1Department of Cardiology, Sri Ramachandra Institute of Higher Education & Research (SRIHER), Chennai, India.
Insights
Clonal hematopoiesis (CHIP) mutations, often overlooked, are linked to cardiovascular diseases (CVD). Targeting CHIP pathways may reduce risks for patients with heart conditions.
Area of Science:
- Genetics and Cardiology
- Hematology and Cardiovascular Medicine
Background:
- Cardiovascular disease (CVD) is a leading global cause of death.
- Established CVD risk factors include dyslipidemia, smoking, diabetes, hypertension, and obesity.
- Overlapping genetic links between other diseases and cardiovascular health are increasingly recognized.
Purpose of the Study:
- To explore the association between clonal hematopoiesis of intermediate potential (CHIP) and cardiovascular diseases (CVD).
- To highlight the potential of targeting CHIP pathways for reducing residual cardiovascular risk.
Main Methods:
- Review of studies identifying mutations (e.g., TET2, DNMT3A, ASXL1, JAK2) causing CHIP.
- Analysis of epidemiological data linking CHIP mutations to specific cardiovascular conditions.
Main Results:
- CHIP, characterized by specific gene mutations, is associated with age-related hematological conditions.
- CHIP mutations are linked to increased risks of coronary artery disease, heart failure, aortic stenosis, and arrhythmias.
- Addressing the CHIP-CVD link presents an opportunity to mitigate cardiovascular risk.
Conclusions:
- The association between CHIP and CVD warrants further investigation.
- Therapeutic strategies targeting inflammasomes, interleukin pathways, or CHIP mutations may offer novel approaches for CVD management.
Abstract:
Cardiovascular disease (CVD) is a major driver of mortality and declining health worldwide. Cardiovascular diseases (CVD) is the most common cause of morbidity and mortality globally. Although dyslipidemia, smoking, diabetes, hypertension and obesity are some well-known causes of CVD, the overlapping genetic pathways between other diseases and those affecting cardiovascular health have been overlooked. In the past decade, mutations in TET2, DNMT3A, ASXL1, and JAK2 are found to cause clonal hematopoiesis of intermediate potential (CHIP), a disease associated with age-related haematological malignancies without the presence of cytopenias or dysplasia. Coronary artery disease, heart failure, aortic stenosis, and arrhythmias have been shown to be associated with the presence of CHIP mutations. Addressing the association between CHIP could significantly reduce residual risk patients with CVD. The link between CHIP and CVD can potentially be addressed through inhibitors of inflammasomes, antagonists in the interleukin pathway, or direct antagonists of CHIP mutations.
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