Clonal hematopoiesis of indeterminate potential: implications for the cardiologists

Author:

Sciatti Edoardo1,D’Elia Emilia1,Gori Mauro1,Grosu Aurelia1,Balestrieri Giulio1,Senni Michele1,Barbui Tiziano2,Gavazzi Antonello2

Affiliation:

1. Cardiology Unit 1, ASST-Papa Giovanni XXIII

2. FROM Research Foundation E.T.S., Papa Giovanni XXIII Hospital, Bergamo, Italy

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

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