Evidence map›Paper›PMID 34735656›Full record

ReviewCurrent oncology reports2021

Is Myelodysplasia a Consequence of Normal Aging?

Sonja Heibl, Reinhard Stauder, Michael Pfeilstöcker

Open access · hybridAbstract readReview
In one paragraph

Review in Current oncology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  4. Review
  5. Observational
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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

3 authors at 3 institutions in 1 country.

Sonja HeiblDepartment of Internal Medicine IV, Klinikum Wels-Grieskirchen, Wels, Austria.ORCID http://orcid.org/0000-0001-8182-990X
Reinhard StauderDepartment of Internal Medicine V, Hematology and Oncology, Comprehensive Cancer Center Innsbruck (CCCI), Medical University of Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0002-8993-9561
Michael Pfeilstöcker3rd Medical Department, Hanusch Hospital, H.Collinstr 30, 1140, Vienna, Austria. michael.pfeilstoecker@oegk.at.ORCID http://orcid.org/0000-0002-1730-6554
Hanusch Hospital · ATInnsbruck Medical University · ATParacelsus Medical University · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewTo review available data on the relationship of MDS and aging and to address the question if biological changes of (premature) aging are a prerequisite for the development of MDS. RECENT

findingsWhereas the association of MDS with advanced age and some common biologic features of aging and MDS are well established, additional evidence for both, especially on the role of stem cells, the stem cell niche, and inflammation, has been recently described. Biologically, many but not all drivers of aging also play a role in the development and propagation of MDS and vice versa. As a consequence, aging contributes to the development of MDS which can be seen as an interplay of clonal disease and normal and premature aging. The impact of aging may be different in specific MDS subtypes and risk groups.

Indexed as

AgingCell Transformation, NeoplasticHematopoiesisHematopoietic Stem CellsHumansMyelodysplastic SyndromesAgingCHIPClonalityElderlyMyelodysplastic syndromesMyeloid neoplasia

Identifiers

PMID34735656
PMCPMC8568861
OpenAlexW3209989713

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.