Connections Between Clonal Hematopoiesis, Cardiovascular Disease, and Cancer: A Review

Oscar Calvillo-Argüelles1,2, Siddhartha Jaiswal3, Liran I Shlush4

  • 1Ted Rogers Program in Cardiotoxicity Prevention, Toronto General Hospital, Toronto, Ontario, Canada.

JAMA Cardiology
|March 14, 2019
PubMed

Insights

Clonal hematopoiesis (CH), an age-associated expansion of mutated blood cells, increases cancer and cardiovascular disease (CVD) risk. This condition may link these diseases, offering new avenues for cardio-oncology treatments.

Area of Science:

  • Hematology
  • Oncology
  • Cardiology
  • Genetics

Background:

  • Clonal hematopoiesis (CH) is an age-associated condition characterized by the expansion of hematopoietic stem cell clones with somatic mutations.
  • CH is increasingly recognized as a significant risk factor for both hematological malignancies and cardiovascular diseases (CVD).
  • This review explores the role of CH as a potential unifying factor linking cancer and CVD.

Purpose of the Study:

  • To review the current understanding of clonal hematopoiesis (CH).
  • To discuss the association between CH, cancer, and cardiovascular disease (CVD).
  • To highlight CH as a potential link between cancer and CVD and its implications for cardio-oncology.

Main Methods:

  • Literature review of studies investigating clonal hematopoiesis.
  • Analysis of the association between CH and the risk of hematological malignancies.
  • Examination of the link between CH and cardiovascular disease (CVD) risk factors and outcomes.

Main Results:

  • CH prevalence increases with age, affecting over 15-20% of individuals aged 90+.
  • CH is associated with a 0.5-1.0% annual risk of hematological malignancy and a 2-4 fold increased risk of CVD.
  • The association between CH and CVD appears causal, potentially mediated by inflammation, and is independent of traditional CVD risk factors.

Conclusions:

  • Clonal hematopoiesis (CH) represents a premalignant state and a significant risk factor for cardiovascular disease (CVD), possibly through inflammatory pathways.
  • CH may also play a role in CVD among cancer survivors, though further research is needed.
  • Advancements in sequencing may enable precision medicine approaches in cardio-oncology by identifying CH.
Abstract

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