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Bone Marrow Transplantation Procedures in Mice to Study Clonal Hematopoiesis
Published on: May 26, 2021
Clonal hematopoiesis of indeterminate potential: implications for the cardiologists
Edoardo Sciatti1, Emilia D'Elia1, Mauro Gori1
1Cardiology Unit 1, ASST-Papa Giovanni XXIII.
Insights
Somatic gene mutations in bone marrow stem cells can lead to clonal hematopoiesis of indeterminate potential (CHIP), causing inflammation and increasing cardiovascular risks like heart attack and stroke.
Area of Science:
- Hematology
- Cardiology
- Immunology
Background:
- Myeloproliferative neoplasms (MPNs) share somatic gene mutations in bone marrow stem cells, linked to cardiovascular complications via inflammation.
- Similar mutations are now identified in cardiovascular disease patients without MPNs, defining clonal hematopoiesis of indeterminate potential (CHIP).
Approach:
- This review examines the link between clonal hematopoiesis, chronic inflammation, and cardiovascular diseases.
- Focuses on a practical approach to enhance clinical practice and identify knowledge gaps.
Key Points:
- CHIP, an age-related condition, is associated with increased risks of myocardial infarction, stroke, and heart failure.
- The underlying genetic mutations in CHIP drive systemic chronic inflammation, contributing to cardiovascular events.
- Understanding this link is crucial for managing patients with CHIP and cardiovascular disease.
Conclusions:
- Clonal hematopoiesis is an emerging driver of cardiovascular disease through inflammatory pathways.
- Further research is needed to develop targeted therapies and improve clinical management for CHIP patients.
- Bridging hematology and cardiology is essential for addressing the unmet needs in this field.
Abstract:
Myeloproliferative neoplasms, including polycythemia vera, essential thrombocythemia, and myelofibrosis, are characterized by somatic gene mutations in bone marrow stem cells, which trigger an inflammatory response influencing the development of associated cardiovascular complications. In recent years, the same mutations were found in individuals with cardiovascular diseases even in the absence of hematological alterations. These genetic events allow the identification of a new entity called 'clonal hematopoiesis of indeterminate potential' (CHIP), as it was uncertain whether it could evolve toward hematological malignancies. CHIP is age-related and, remarkably, myocardial infarction, stroke, and heart failure were frequently reported in these individuals and attributed to systemic chronic inflammation driven by the genetic mutation. We reviewed the connection between clonal hematopoiesis, inflammation, and cardiovascular diseases, with a practical approach to improve clinical practice and highlight the current unmet needs in this area of knowledge.
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