医学
原发性血小板增多症
骨髓纤维化
真性红细胞增多症
造血
骨髓
炎症
体细胞
心肌梗塞
髓外造血
基因突变
干细胞
生物信息学
突变
免疫学
病理
内科学
基因
遗传学
生物
作者
Edoardo Sciatti,Emilia D’Elia,Mauro Gori,Aurelia Grosu,Giulio Balestrieri,Michele Senni,Tiziano Barbui,Antonello Gavazzi
出处
期刊:Journal of Cardiovascular Medicine
[Ovid Technologies (Wolters Kluwer)]
日期:2023-11-25
卷期号:25 (1): 1-12
标识
DOI:10.2459/jcm.0000000000001520
摘要
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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