Evidence map›Paper›PMID 38359296›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

The impact of age and number of mutations on the size of clonal hematopoiesis.

Kai Wang, Wen Zhang, Li Yi, Ming Zhao, Peng-Yu Li, Mei-Hong Fu, Rong Lin, Yong-Mei Zhu, Jian-Feng Li, Wei-Ping Yang and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
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  4. Article
  5. Review
  6. African journal of laboratory medicine · 2026
    Article
  7. Article
  8. Aging and immunity: the age-old tango.Genes & development · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Aging and comprehensive molecular profiling in acute myeloid leukemia.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Kai Wang *International Center for Aging and Cancer, Department of Hematology of The First Affiliated Hospital, Hainan Medical University, Haikou 571199, China.ORCID 0000-0002-4145-9569
Wen Zhang *Department of Biochemistry and Molecular Biology, Key Laboratory of Molecular Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou 571199, China.ORCID 0009-0007-1015-2197
Li Yi *International Center for Aging and Cancer, Department of Hematology of The First Affiliated Hospital, Hainan Medical University, Haikou 571199, China.ORCID 0009-0008-5585-8975
Ming ZhaoInternational Center for Aging and Cancer, Department of Hematology of The First Affiliated Hospital, Hainan Medical University, Haikou 571199, China.
Peng-Yu LiInternational Center for Aging and Cancer, Department of Hematology of The First Affiliated Hospital, Hainan Medical University, Haikou 571199, China.ORCID 0009-0002-8803-5680
Mei-Hong FuInternational Center for Aging and Cancer, Department of Hematology of The First Affiliated Hospital, Hainan Medical University, Haikou 571199, China.ORCID 0009-0006-2215-8046
Rong LinDepartment of Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou 571199, China.ORCID 0000-0001-9161-6844
Yong-Mei ZhuShanghai Institute of Hematology, State Key Laboratory for Medical Genomics, National Research Center for Translational Medicine, Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Jian-Feng LiShanghai Institute of Hematology, State Key Laboratory for Medical Genomics, National Research Center for Translational Medicine, Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.ORCID 0000-0003-2349-208X
Wei-Ping YangInternational Center for Aging and Cancer, Department of Hematology of The First Affiliated Hospital, Hainan Medical University, Haikou 571199, China.
Hai FangShanghai Institute of Hematology, State Key Laboratory for Medical Genomics, National Research Center for Translational Medicine, Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.ORCID 0000-0003-3961-8572
Zhu ChenShanghai Institute of Hematology, State Key Laboratory for Medical Genomics, National Research Center for Translational Medicine, Ruijin Hospital affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.ORCID 0000-0002-2968-7665
Wang-Wei CaiDepartment of Biochemistry and Molecular Biology, Key Laboratory of Molecular Biology, School of Basic Medicine and Life Sciences, Hainan Medical University, Haikou 571199, China.ORCID 0000-0002-7714-2790
Rui-Bao RenInternational Center for Aging and Cancer, Department of Hematology of The First Affiliated Hospital, Hainan Medical University, Haikou 571199, China.
Hainan Medical University · CNShanghai Jiao Tong University · CN

Funding

Hainan Provincial Department of Science and Technology () 2023ICAC-YANFAHainan Provincial Department of Science and Technology () 2023ICAC-YUNXINGMOST | National Natural Science Foundation of China (NSFC) 32170663Shanghai Collaborative Innovation Program on Regenerative Medicine and Stem Cell Research 2019CXJQ01Shanghai Science and Technology Development Funds 20Z11900200the Innovative Research Team of High-level Local Universities in Shanghai NAthe Samuel Waxman Cancer Research Foundation NA
6 · The paper itself

Abstract

Clonal hematopoiesis (CH) represents the clonal expansion of hematopoietic stem cells and their progeny driven by somatic mutations. Accurate risk assessment of CH is critical for disease prevention and clinical decision-making. The size of CH has been showed to associate with higher disease risk, yet, factors influencing the size of CH are unknown. In addition, the characteristics of CH in long-lived individuals are not well documented. Here, we report an in-depth analysis of CH in longevous (≥90 y old) and common (60~89 y old) elderly groups. Utilizing targeted deep sequencing, we found that the development of CH is closely related to age and the expression of aging biomarkers. The longevous elderly group exhibited a significantly higher incidence of CH and significantly higher frequency of

Indexed as

Clonal HematopoiesisHematopoiesisAgedAgingBiomarkersHumansMutationBiomarkersagingclonal hematopoiesismutationstargeted DNA sequencing

Identifiers

PMID38359296
PMCPMC10895265
OpenAlexW4391838789

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.