Clonal haematopoiesis and cardiovascular diseases: A growing relationship

Sami Fawaz1, Olivier Mansier2, Yann Pucheu3

  • 1Centre d'exploration, de prévention et de traitement de l'athérosclérose (CEPTA), CHU Bordeaux, 33000 Bordeaux, France.

Insights

Clonal haematopoiesis of indeterminate potential (CHIP) is linked to increased cardiovascular disease risk. Understanding CHIP mechanisms may improve patient care and risk prediction for conditions like heart attack and heart failure.

Area of Science:

  • Cardiovascular Medicine
  • Hematology
  • Immunology

Background:

  • Cardiovascular diseases, especially atherothrombosis, are leading global causes of mortality.
  • Established risk factors inadequately predict individual cardiovascular risk.
  • Clonal haematopoiesis of indeterminate potential (CHIP) is a recently identified condition involving clonal expansion of hematopoietic cells due to somatic mutations, prevalent in older adults.

Purpose of the Study:

  • To review current knowledge on CHIP and its cardiovascular implications.
  • To explore the pathophysiological mechanisms linking CHIP to increased cardiovascular risk.
  • To discuss the potential impact of CHIP on clinical practice and patient management.

Main Methods:

  • Literature review of observational and experimental studies.
  • Analysis of the role of inflammation and immune cells, specifically IL-1β-secreting macrophages.
  • Synthesis of findings related to CHIP's effect on atherosclerotic plaques and myocardial tissue.

Main Results:

  • CHIP is associated with a higher risk of myocardial infarction, heart failure, and severe aortic valve stenosis.
  • CHIP presence appears to negatively impact the prognosis of these cardiovascular conditions.
  • Inflammation, mediated by IL-1β-secreting macrophages, is a key mechanism linking CHIP to cardiovascular pathology.

Conclusions:

  • CHIP represents a significant, emerging risk factor for cardiovascular diseases.
  • Understanding the inflammatory pathways involved in CHIP is crucial for developing targeted therapies.
  • Integrating CHIP assessment into clinical practice may enhance cardiovascular risk stratification and patient care.

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