Evidence map›Paper›PMID 28483762›Full record

ArticleBlood2017

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.

Florian Zink, Simon N Stacey, Gudmundur L Norddahl, Michael L Frigge, Olafur T Magnusson, Ingileif Jonsdottir, Thorgeir E Thorgeirsson, Asgeir Sigurdsson, Sigurjon A Gudjonsson, Julius Gudmundsson and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 498 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
498citing papers in PubMed, 3 pooled it
47.2field-weighted citation impact, top 1% 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

498 citing papers in PubMed, 3 syntheses or guidelines pooled it, 776 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Mosaic Chromosomal Alterations and Human Longevity.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Pooled it
  4. Trial
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  6. Trial
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
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  14. Article
  15. Review
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  17. Article
  18. Genetic influences on haematopoiesis.Nature reviews. Genetics · 2026
    Review
  19. Article
  20. Article

438 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 4 institutions in 1 country.

Florian ZinkdeCODE genetics/AMGEN, Reykjavik, Iceland.
Simon N StaceydeCODE genetics/AMGEN, Reykjavik, Iceland.
Gudmundur L NorddahldeCODE genetics/AMGEN, Reykjavik, Iceland.
Michael L FriggedeCODE genetics/AMGEN, Reykjavik, Iceland.
Olafur T MagnussondeCODE genetics/AMGEN, Reykjavik, Iceland.
Ingileif JonsdottirdeCODE genetics/AMGEN, Reykjavik, Iceland.
Thorgeir E ThorgeirssondeCODE genetics/AMGEN, Reykjavik, Iceland.
Asgeir SigurdssondeCODE genetics/AMGEN, Reykjavik, Iceland.
Sigurjon A GudjonssondeCODE genetics/AMGEN, Reykjavik, Iceland.
Julius GudmundssondeCODE genetics/AMGEN, Reykjavik, Iceland.
Jon G JonassonLandspitali-University Hospital, Reykjavik, Iceland.
Laufey TryggvadottirIcelandic Cancer Registry, Reykjavik, Iceland; and.
Thorvaldur JonssonLandspitali-University Hospital, Reykjavik, Iceland.
Agnar HelgasondeCODE genetics/AMGEN, Reykjavik, Iceland.
Arnaldur GylfasondeCODE genetics/AMGEN, Reykjavik, Iceland.
Patrick SulemdeCODE genetics/AMGEN, Reykjavik, Iceland.
Thorunn RafnardeCODE genetics/AMGEN, Reykjavik, Iceland.
Unnur ThorsteinsdottirdeCODE genetics/AMGEN, Reykjavik, Iceland.
Daniel F GudbjartssondeCODE genetics/AMGEN, Reykjavik, Iceland.
Gisli MassondeCODE genetics/AMGEN, Reykjavik, Iceland.
Augustine KongdeCODE genetics/AMGEN, Reykjavik, Iceland.
Kari StefanssondeCODE genetics/AMGEN, Reykjavik, Iceland.
deCODE Genetics (Iceland) · ISUniversity of Iceland · ISNational University Hospital of Iceland · ISIcelandic Cancer Society · IS

Funding

Genes contributing to nicotine dependence in humansR01DA017932 · NIDA · DECODE GENETICS, INC. · PI STEFANSSON, KARI · 2005 to 2015
$9.6M
Identifying Amphetamine Addiction Risk Variants by Whole Genome SequencingR01DA034076 · NIDA · DECODE GENETICS, EHF · PI THORGEIRSSON, THORGEIR E. · 2013 to 2017
$2.6M
NIDA NIH HHS R01 DA017932NIDA NIH HHS R01 DA034076
6 · The paper itself

Abstract

Clonal hematopoiesis (CH) arises when a substantial proportion of mature blood cells is derived from a single dominant hematopoietic stem cell lineage. Somatic mutations in candidate driver (CD) genes are thought to be responsible for at least some cases of CH. Using whole-genome sequencing of 11 262 Icelanders, we found 1403 cases of CH by using barcodes of mosaic somatic mutations in peripheral blood, whether or not they have a mutation in a CD gene. We find that CH is very common in the elderly, trending toward inevitability. We show that somatic mutations in

Indexed as

HematopoiesisMutationAdultAgedAged, 80 and overAge FactorsClone CellsDioxygenasesDNA-Binding ProteinsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3AFemaleHematologic NeoplasmsHematopoietic Stem CellsHumansMaleASXL1 protein, humanDioxygenasesDNA-Binding ProteinsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNMT3A protein, humanPPM1D protein, humanProtein Phosphatase 2CProto-Oncogene ProteinsRepressor ProteinsTET2 protein, human

Identifiers

PMID28483762
PMCPMC5553576
OpenAlexW2612571615

What OpenQuestion holds

Textmetadata
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.