Clonal hematopoiesis and non-hematologic disorders
Open accessAbstract
Clonal expansions of mutated hematopoietic cells, termed clonal hematopoiesis, are common in aging humans. One expected consequence of mutation-associated clonal hematopoiesis is an increased risk of hematologic cancers, which has now been shown in several studies. However, the hematopoietic stem cells that acquire these somatic mutations also give rise to mutated immune effector cells, such as monocytes, granulocytes, and lymphocytes. These effector cells can potentially influence many disease states, especially those with a chronic inflammatory component. Indeed, several studies have now shown that clonal hematopoiesis associates with increased risk of atherosclerotic cardiovascular disease. Emerging data also associate clonal hematopoiesis to other non-hematologic diseases. Here, we will review recent studies linking clonal hematopoiesis to altered immune function, inflammation, and non-malignant diseases of aging.
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CHIP is associated with increased all-cause mortality and a broad spectrum of non-malignant diseases, most prominently atherosclerotic cardiovascular disease and stroke.
“CHIP has emerged as a clinically relevant state associated with increased all-cause mortality and a broad spectrum of non-malignant diseases, most prominently atherosclerotic cardiovascular disease and stroke [1,4,5].”
CHIP robustly increases the risk of atherosclerotic cardiovascular disease, ischemic stroke, and cerebral small vessel disease, conditions that independently contribute to cognitive impairment and dementia.
“CHIP robustly increases the risk of atherosclerotic cardiovascular disease, ischemic stroke, and cerebral small vessel disease, conditions that independently contribute to cognitive impairment and dementia [4,5,15,16].”
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References 108 · Cited by 182
- Authors
- Jaiswal, S.
- Affiliations
- Stanford University (US)
- Corresponding author
- Jaiswal, Siddhartha
- ORCID
- Jaiswal, Siddhartha
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2020-07-31
- Volume
- 136
- Issue
- 14
- Pages
- 1606-1614
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- PMC
- PMC8209629
- OpenAlex
- W3046552632
- Cited by
- 182
- References
- 108
- Citations by year
- 2026: 9 · 2025: 35 · 2024: 42 · 2023: 36 · 2022: 40 · 2021: 17 · 2020: 3
- FWCI
- 15.16
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Blood (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (DP2HL157540)
- National Cancer Institute (K08CA204734, T32CA009172)
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Health Sciences › Medicine › Genetics › Myeloproliferative Neoplasms: Diagnosis and Treatment
- Keywords
- clonal hematopoiesis, somatic mutations, hematopoietic stem cells, atherosclerotic cardiovascular disease, chronic inflammation, immune function, aging, monocytes, granulocytes, lymphocytes
- MeSH terms
- Clonal Hematopoiesis, Animals, Cardiovascular Diseases, Disease Susceptibility, Hematopoiesis, Humans, Mutation, Terminology as Topic, Organ Specificity, Phenotype, Biomarkers, Genetic Predisposition to Disease, Genetic Association Studies, Clonal Evolution
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