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DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions
Open accessAbstract
had no impact on blood counts or indices. Mutational burden of both genes correlated with X-inactivation skewing but no significant association with age-adjusted telomere length reduction was documented. The discordance between the high prevalence of mutations in these 2 genes and their limited biological impact raise the question of the potential role of dysregulated epigenetic modifiers in normal aging hematopoiesis, which may include support to failing hematopoiesis.
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“Other studies have found links between CHIP and chronic obstructive pulmonary disease (COPD) 37,63.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [63]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Various other systemic effects have been described in association with CH, including chronic obstructive pulmonary disease and other pulmonary disease [16,33,34]”
From Clonal hematopoiesis and inflammation – the perpetual cycle (2023) · cites this paper as [33]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Loss-of-function heterozygous mutations in epigenetic regulators DNMT3A (cytosine methyltransferase) and TET2 (methylcytosine dioxygenase) are the most frequently detected mutations in CHIP, accounting for about 50% to 60% and 10% to 30% of mutations found in CHIP carriers, respectively.1, 2, 3,7,8”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the context of CHIP, TET2 mutations show highest clonal expansion rates over time (with an estimated 10% annual growth rate compared with 5% of DNMT3A mutations7,8,10).”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Loss-of-function heterozygous mutations in epigenetic regulators DNMT3A (cytosine methyltransferase) and TET2 (methylcytosine dioxygenase) are the most frequently detected mutations in CHIP, accounting for about 50% to 60% and 10% to 30% of mutations found in CHIP carriers, respectively.1, 2, 3,7,8”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
Experimental — accuracy not yet measured
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In the citing paper
“are predicted to have high expansion rates (10% increase in mean VAF per year1, 2, 3,7)”
From Aging drives Tet2 +/− clonal hematopoiesis via IL-1 signaling (2023) · cites this paper as [7]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“many have noted that DNMT3A mutations confer little phenotype on steady state hematopoiesis (Buscarlet et al., 2017)”
From Chronic infection drives Dnmt3a-loss-of-function clonal hematopoiesis via IFNγ signaling (2021) · cites this paper as Buscarlet et al., 2017
In the citing paper
“CHIP itself does not denote a malignancy, nor is it associated with clinically significant alterations in blood counts 28,63.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [63]
In the citing paper
“However, CHIP was also strongly linked to smoking in these studies, so the result could be confounded by this association.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [63]
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Citations
Cites
Signatures of mutational processes in human cancer
Initiative, A. P. C. G., Alexandrov, L. B., ICGC Breast Cancer Consortium, ICGC MMML-Seq Consortium, PedBrain, I., Nik-Zainal, S., Wedge, D. C., Aparicio, S. A. J. R., Behjati, S., Biankin, A. V., et al. (2013) · Nature · doi:10.1038/nature12477 · Cited by 9,660
Age-related clonal hematopoiesis associated with adverse outcomes
Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1408617 · Cited by 4,841
Telomere measurement by quantitative PCR
Cawthon, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.10.e47 · Cited by 3,550
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
Genovese, G., Kähler, A. K., Handsaker, R. E., Lindberg, J., Rose, S. A., Bakhoum, S. F., Chambert, K., Mick, E., Neale, B. M., Fromer, M., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1409405 · Cited by 3,531
Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes
Steensma, D. P., Bejar, R., Jaiswal, S., Lindsley, R. C., Sekeres, M. A., Hasserjian, R. P., & Ebert, B. L. (2015) · Blood · doi:10.1182/blood-2015-03-631747 · Cited by 1,971
Age-related mutations associated with clonal hematopoietic expansion and malignancies
Xie, M., Lu, C., Wang, J., McLellan, M. D., Johnson, K. J., Wendl, M. C., McMichael, J. F., Schmidt, H. K., Yellapantula, V., Miller, C. A., et al. (2014) · Nature Medicine · doi:10.1038/nm.3733 · Cited by 1,874
Allen, R. C., Zoghbi, H. Y., Moseley, A., Rosenblatt, H. M., & Belmont, J. W. (1992) · PubMed · Cited by 1,683
The origin and evolution of mutations in acute myeloid leukemia
Welch, J. S., Ley, T. J., Link, D. C., Miller, C. A., Larson, D. E., Koboldt, D. C., Wartman, L. D., Lamprecht, T. L., Liu, F., Xia, J., et al. (2012) · Cell · doi:10.1016/j.cell.2012.06.023 · Cited by 1,575
Guralnik, J. M., Eisenstaedt, R. S., Ferrucci, L., Klein, H. G., & Woodman, R. C. (2004) · Blood · doi:10.1182/blood-2004-05-1812 · Cited by 1,450
Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia
Shlush, L. I., Zandi, S., Mitchell, A., Chen, W. C., Brandwein, J. M., Gupta, V., Kennedy, J. A., Schimmer, A. D., Schuh, A. C., Yee, K. W., et al. (2014) · Nature · doi:10.1038/nature13038 · Cited by 1,443
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Eadie, L. N., Rehn, J. A., Schutz, C. E., Heatley, S. L., Kutyna, M., Hiwase, D., White, D. L., & Yeung, D. T. O. (2023) · British Journal of Haematology · doi:10.1111/bjh.19008 · Cited by 2
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Yu, X., Qian, N., & Wang, Y. (2023) · Molecular Biology Reports · doi:10.1007/s11033-022-08118-1 · Cited by 2
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McClatchy, J., Strogantsev, R., Wolfe, E., Lin, H., Mohammadhosseini, M., Davis, B. A., Eden, C. O., Goldman, D., Fleming, W., Conley, P., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.15.507688 · Cited by 2
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Verma, D., Zeig‐Owens, R., Goldfarb, D. G., Kravets, L., Pradhan, K., Rockwell, B., Sahu, S., Kelly, S., Giricz, O., Jasra, S., et al. (2025) · Cancer Discovery · doi:10.1158/2159-8290.cd-24-1590 · Cited by 2
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Wang, L., Chien, W., Sheng‐Kai, K., Chung, C., Chen, Y., Tsai, W.-C., & Yang, B.-H. (2025) · PLoS Medicine · doi:10.1371/journal.pmed.1004646 · Cited by 1
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Zhang, Z., An, Y., Yang, M., Pan, Y., Liu, X., Gong, F., Lin, H., Tang, B., Wang, W., Bai, Y., et al. (2026) · Advanced Science · doi:10.1002/advs.202514819 · Cited by 1
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Singh, J., Curtis, D. J., Thảo, L. T. P., Wood, E. M., & McQuilten, Z. (2026) · Aging Cell · doi:10.1111/acel.70425 · Cited by 1
Ma, X., Yang, C. H., Duan, Y., Zhang, H., Tang, X., Zhang, Q., Qin, W., Zhang, W., Tang, G., Guan, M., et al. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1771587 · Cited by 1
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Myers, J., Worthington, A. K., Poscablo, D. M., Medina, P., Chattopadhyaya, S., Mogharrab, R., Rommel, M. G. E., & Forsberg, E. C. (2026) · Stem Cell Reports · doi:10.1016/j.stemcr.2026.102965 · Cited by 3
Chen, S., Chen, H.-W., Chu, C. H., Hsu, P., Yu, Y.-S., Lin, S., Wu, Y.-X., Lin, E. C., Lin, T.-A., Chen, M.-H., et al. (2026) · Mitochondrion · doi:10.1016/j.mito.2026.102192 · Cited by 1
Al-Ansari, R. Y., Otaibi, D. A., Hudaithi, N. A., & Abdalla, L. (2021) · SAGE Open Medical Case Reports · doi:10.1177/2050313x211032066 · Cited by 1
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Craig, J. M., Gerhard, G. S., Sharma, S., Yankovskiy, A., Miura, S., & Kumar, S. (2023) · Molecular Biology and Evolution · doi:10.1093/molbev/msad279 · Cited by 1
Li, J., Qi, Z., Xu, Y., Cao, Y., Li, Y., & Han, Y. (2024) · Cardiology Discovery · doi:10.1097/cd9.0000000000000139 · Cited by 1
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Lawrence, E., Cooray, A., Kueh, A. J., Pál, M., Tai, L., Garnham, A. L., Suen, C. S. N. L. W., Vanyai, H. K., Gouil, Q. A., Lancaster, J., et al. (2025) · EMBO Reports · doi:10.1038/s44319-025-00450-4 · Cited by 1
Krishnan, A., Miles, L. A., & Challen, G. A. (2025) · Experimental Hematology · doi:10.1016/j.exphem.2025.104816 · Cited by 1
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Götze, K. S. S., & Lengerke, C. (2022) · Die Innere Medizin · doi:10.1007/s00108-022-01401-0 · Cited by 1
Gillis, N., Moscinski, L. C., & Padron, E. (2018) · Springer eBooks · doi:10.1007/978-3-319-44870-1_57-1 · Cited by 1
González‐Gil, C., Morgades, M., Lopes, T., Fuster‐Tormo, F., García-Chica, J., Zhao, R., Montesinos, P., Torrent, A., Díaz‐Beyá, M., Coll, R., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4068248 · Cited by 1
Dawoud, A. A. Z., Tapper, W., & Cross, N. C. P. (2022) · medRxiv · doi:10.1101/2022.09.05.22279615 · Cited by 1
Páramo, J. A. (2018) · Medicina Clínica · doi:10.1016/j.medcli.2018.04.007
Páramo, J. A. (2018) · Medicina Clínica (English Edition) · doi:10.1016/j.medcle.2018.07.006
Clonal Hematopoiesis and Cytopenias in the Elderly
Guy, D. G., Afzal, A., & Jacoby, M. A. (2018) · Springer eBooks · doi:10.1007/978-3-319-96487-4_12
Genetics and Pharmacogenetics of COPD
Bossé, Y., & Cho, M. H. (2020) · Respiratory medicine · doi:10.1007/978-3-030-31507-8_4
A view from the hospital window.
Richards, A. G. (1974) · PubMed
Проблемы при реализации креативного менеджмента в организации
Цыганкова, В. Н. (2010) · Креативная экономика
Murakami, K., Yamaguchi, Y., Kida, Y., Morikawa, Y., Ujiie, H., Sugahara, H., Nannya, Y., Ogawa, S., & Kanakura, Y. (2021) · Internal Medicine · doi:10.2169/internalmedicine.7571-21
Афанасьев, Д. Е. (2008) · CyberLeninK (CyberLeninka)
COPD makes CHIP less indeterminate
Huls, G. A. (2022) · Blood · doi:10.1182/blood.2021013966
Gillis, N., Moscinski, L. C., & Padron, E. (2020) · Springer eBooks · doi:10.1007/978-3-319-57415-8_57 · Cited by 1
González‐Gil, C., Morgades, M., Lopes, T., Fuster‐Tormo, F., García-Chica, J., Zhao, R., Montesinos, P., Torrent, A., Díaz‐Beyá, M., Coll, R., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1377009/v1
Sperling, A. S., & Ebert, B. L. (2017) · Blood · doi:10.1182/blood-2017-05-786210
Faculty Opinions recommendation of Understanding intrinsic hematopoietic stem cell aging.
Méndez‐Ferrer, S. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737043526.793575345
Klonale Hämatopoese – Ursachen und klinische Implikationen
Burchert, A. (2022) · Die Innere Medizin · doi:10.1007/s00108-022-01388-8
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Xie, Z., Chen, E. C., Mendez, L., Komrokji, R. S., & Zeidan, A. M. (2023) · The Cancer Journal · doi:10.1097/ppo.0000000000000656
EXABS-171-MDS Update on CHIP and CCUS
Weeks, L. D. (2023) · Clinical Lymphoma Myeloma & Leukemia · doi:10.1016/s2152-2650(23)00310-5
Impact of clonal hematopoiesis in COVID-19 patients at high risk for adverse clinical outcomes
Smith, C., Burugula, B. B., Jones, M. A., Li, Q., Kitzman, J. O., & Wong, T. (2023) · Translational Medicine Communications · doi:10.1186/s41231-023-00155-7
Pietka, G., Lord, C. D., Matthias, G., Cheung, B. Y. Y., Atwal, S., Furtado, M., Cullis, J., Grey‐Davies, L., Narayanan, S., McGregor, A. K., et al. (2024) · British Journal of Haematology · doi:10.1111/bjh.19377
Bonadies, N. (2024) · healthbook TIMES Oncology Hematology · doi:10.36000/hbt.oh.2024.19.136
Lawrence, E., Cooray, A., Kueh, A. J., Pál, M., Tai, L., Garnham, A. L., Suen, C. S. N. L. W., Vanyai, H. K., Gouil, Q. A., Lancaster, J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.12.607467
Leddin, E. M. (2022) · University of North Texas Digital Library (University of North Texas) · doi:10.12794/metadc1944361
Jarabek, A., Davis, X. D., Oliver, M., Wang, Y., Chen, H., Bohannon, J. K., & Zinkel, S. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.08.674943
He, X., Jia, Z.-N., Wu, J.-Z., Lv, J., Liu, Z., Liu, L., Liu, R.-L., Yuan, K., Yang, K., Li, C.-C., et al. (2025) · Discover Medicine · doi:10.1007/s44337-025-00281-1
Sun, H., Ruijie, L., Cao, X., Wang, H., Ding, P., Ang, Y., & Guo, X. (2025) · Clinical Research in Cardiology · doi:10.1007/s00392-025-02823-0
Smith, C., Burugula, B. B., Jones, M. A., Li, Q., Kitzman, J. O., & Wong, T. N. (2023) · Figshare · doi:10.6084/m9.figshare.24225240
Smith, C., Burugula, B. B., Jones, M. A., Li, Q., Kitzman, J. O., & Wong, T. N. (2024) · Figshare · doi:10.6084/m9.figshare.24225247
Dalle, I. A., Galimard, J., Poiré, X., Sanz, J. L. V., Huynh, A., Kröger, N. M., Wagner-Drouet, E., Burns, D., Eder, M., Lioure, B., et al. (2025) · Bone Marrow Transplantation · doi:10.1038/s41409-025-02765-1
Barton, J. C., & Barton, J. C. (2026) · The American Journal of the Medical Sciences · doi:10.1016/j.amjms.2026.01.004
Lee, N. C. J., Miao, R., & Young, N. S. (2026) · Leukemia · doi:10.1038/s41375-026-02865-x
Bagacean, C. (2018) · theses.fr (ABES) · doi:10.70675/4409fbafz6d37z497cza3b9zf76d4e09d242
Modifications du microenvironnement cytokinique dans les leucémies aigües myéloïdes
Guermouche, H. (2021) · theses.fr (ABES) · doi:10.70675/e0e649a1z9428z4e58z93b3z0b5d7ec2fea8
Pegliasco, J. (2024) · theses.fr (ABES) · doi:10.70675/12ce08e6zd564z4165zaee7zd80d8186dafd
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Liquid biopsy for molecular profiling in cutaneous T-cell lymphoma: a pilot feasibility study
Sacknovitz, Y., Erem, A. S., Kent, J., Albitar, M. X., Feldman, T. A., Pro, B., Tolu, S. S., Gru, A. A., & Geskin, L. J. (2026) · Blood Neoplasia · doi:10.1016/j.bneo.2026.100245
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Ramos-Neble, B. L., & Fuster, J. J. (2026) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2026.120718
Papasavva, P. L., Dosunmu-Ogunbi, A. M., Oni, M. O., Kountouris, P., Makani, J., Zilfalil, B. A., Inusa, B. P. D., Archer, N. M., Lederer, C. W., Ahmad, H., et al. (2026) · Blood Advances · doi:10.1182/bloodadvances.2025018935
Powell, N., Cubbon, R. M., Bailey, M. A., Griffin, K. J., Roberts, L. D., & Cheng, C. W. (2026) · Vascular Medicine · doi:10.1177/1358863x261437058
Hasan, M., Durandeau, S., Thompson, I. R., Roussotte, H., Tsai, Y.-T., Seymen, N., Gerlevik, S., Bianchini, N., Alishah, K., Albuquerque, M. M., et al. (2026) · GeroScience · doi:10.1007/s11357-026-02510-6
Ünsal, Ş. E. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1943135
Somatic Blood Mosaicism and Psychiatric Disease: Current Evidence and Causal Limits
Belbe, A.-A., Pîrlog, L.-M., Pilatec, A.-N., Militaru, M.-S., Iordănescu, I. I., & Cătană, A. (2026) · Genes · doi:10.3390/genes17101224
TET2-driven activation of AGO2 links epigenetic remodeling to myeloid commitment and leukemia
Lazarenkov, A., Valcárcel, G., Martínez-Moreno, A., Berenguer, C., López-Rubio, A. V., Obiols, M., Fontanet, C., Barbă, A., Rodríguez‐Sevilla, J. J., Stik, G., et al. (2026) · Science Advances · doi:10.1126/sciadv.aee5701
Metadata
- Authors
- Buscarlet, M., Provost, S., Zada, Y. F., Barhdadi, A., Bourgoin, V., Lépine, G., Mollica, L., Szuber, N., Dubé, M.-P., & Busque, L.
- Affiliations
- Hôpital Maisonneuve-Rosemont (CA)
- Montreal Heart Institute (CA)
- ORCID
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2017-08-10
- Volume
- 130
- Issue
- 6
- Pages
- 753-762
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W2728241634
- Cited by
- 383
- References
- 50
- Citations by year
- 2026: 22 · 2025: 34 · 2024: 37 · 2023: 47 · 2022: 59 · 2021: 55 · 2020: 46 · 2019: 40 · 2018: 34 · 2017: 6
- FWCI
- 26.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Blood (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Concordia University
- Canadian Institutes of Health Research
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Keywords
- DNMT3A, TET2, clonal hematopoiesis, somatic mutations, X-inactivation skewing, telomere length, epigenetic regulators, genetic susceptibility, mutational burden
- MeSH terms
- DNA Methyltransferase 3A, Age Factors, Aged, Aged, 80 and over, Aging, Blood Cell Count, Clone Cells, DNA (Cytosine-5-)-Methyltransferases, DNA-Binding Proteins, Female, Hematopoiesis, Humans, Male, Middle Aged, Mutation, Proto-Oncogene Proteins, Cohort Studies, Hematologic Neoplasms, Genetic Predisposition to Disease, Dioxygenases, X Chromosome Inactivation, High-Throughput Nucleotide Sequencing, Telomere Homeostasis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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