Evidence map›Paper›PMID 30158459›Full record

ReviewInternational journal of molecular sciences2018

Updates on Old and Weary Haematopoiesis.

Joanna Konieczny, Lorena Arranz

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Mosaic Chromosomal Alterations and Human Longevity.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Pooled it
  2. Review
  3. Article
  4. Biomarkers of aging.Science China. Life sciences · 2023
    Review
  5. Review
  6. Review
  7. Prostaglandin EStem cell reviews and reports · 2021
    Article
  8. JAK-STAT in Early Hematopoiesis and Leukemia.Frontiers in cell and developmental biology · 2021
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Where Could Research on Immunosenescence Lead?International journal of molecular sciences · 2019
    Article
  14. Review
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

2 authors at 2 institutions in 1 country.

Joanna KoniecznyStem Cell Aging and Cancer Research Group, Department of Medical Biology, Faculty of Health Sciences, UiT, The Arctic University of Norway, 9019 Tromsø, Norway. jko029@post.uit.no.
Lorena ArranzStem Cell Aging and Cancer Research Group, Department of Medical Biology, Faculty of Health Sciences, UiT, The Arctic University of Norway, 9019 Tromsø, Norway. lorena.arranz@uit.no.ORCID 0000-0002-5896-4238
UiT The Arctic University of Norway · NOUniversity Hospital of North Norway · NO

Funding

Aakre-Stiftelsen Foundation 2016/9050Northern Norway Regional Health Authority HNF1338-17Northern Norway Regional Health Authority, the University Hospital of Northern Norway (UNN) and UiT The Arctic University of Norway (UiT) 2014/5668Norwegian Cancer Society 6765150Young Research Talent grants from the Research Council of Norway FRIPRO Program, 250901Young Research Talent grants from the Research Council of Norway Stem Cell Program, 247596
6 · The paper itself

Abstract

Blood formation, or haematopoiesis, originates from haematopoietic stem cells (HSCs), whose functions and maintenance are regulated in both cell- and cell non-autonomous ways. The surroundings of HSCs in the bone marrow create a specific niche or microenvironment where HSCs nest that allows them to retain their unique characteristics and respond rapidly to external stimuli. Ageing is accompanied by reduced regenerative capacity of the organism affecting all systems, due to the progressive decline of stem cell functions. This includes blood and HSCs, which contributes to age-related haematological disorders, anaemia, and immunosenescence, among others. Furthermore, chronological ageing is characterised by myeloid and platelet HSC skewing, inflammageing, and expanded clonal haematopoiesis, which may be the result of the accumulation of preleukaemic lesions in HSCs. Intriguingly, haematological malignancies such as acute myeloid leukaemia have a high incidence among elderly patients, yet not all individuals with clonal haematopoiesis develop leukaemias. Here, we discuss recent work on these aspects, their potential underlying molecular mechanisms, and the first cues linking age-related changes in the HSC niche to poor HSC maintenance. Future work is needed for a better understanding of haematopoiesis during ageing. This field may open new avenues for HSC rejuvenation and therapeutic strategies in the elderly.

Indexed as

AgingAnimalsBone MarrowHematopoiesisHumansLeukemiaageingbone marrowclonal haematopoiesishaematopoiesishaematopoietic stem cell nicheinflammageingleukaemia

Identifiers

PMID30158459
PMCPMC6163425
OpenAlexW2889276547

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.