Evidence map›Paper›PMID 30076180›Full record

ReviewHaematologica2018

Normal and pathological erythropoiesis in adults: from gene regulation to targeted treatment concepts.

Peter Valent, Guntram Büsche, Igor Theurl, Iris Z Uras, Ulrich Germing, Reinhard Stauder, Karl Sotlar, Wolfgang Füreder, Peter Bettelheim, Michael Pfeilstöcker and 9 more

Open access · goldAbstract readReview
In one paragraph

Review in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  16. Article
  17. Article
  18. Post-transcriptional regulation of erythropoiesis.Blood science (Baltimore, Md.) · 2023
    Review
  19. Article
  20. CD71Journal for immunotherapy of cancer · 2023
    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

19 authors at 13 institutions in 4 countries.

Peter ValentDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Austria peter.valent@meduniwien.ac.at ohermine@gmail.com.
Guntram BüscheInstitute of Pathology, Medizinische Hochschule Hannover, Germany.
Igor TheurlDepartment of Internal Medicine II, Medical University Innsbruck, Austria.
Iris Z UrasInstitute of Pharmacology and Toxicology, University of Veterinary Medicine, Vienna, Austria.
Ulrich GermingDepartment of Hematology, Oncology and Clinical Immunology, Heinrich-Heine University, Düsseldorf, Germany.
Reinhard StauderDepartment of Internal Medicine V, Medical University Innsbruck, Austria.
Karl SotlarInstitute of Pathology, Paracelsus Medical University Salzburg, Austria.
Wolfgang FürederDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Austria.
Peter BettelheimFirst Department of Internal Medicine, Elisabethinen Hospital, Linz, Austria.
Michael PfeilstöckerLudwig Boltzmann Cluster Oncology, Medical University of Vienna, Austria.
Rainer OberbauerDepartment of Nephrology and Dialysis, Medical University of Vienna, Austria.
Wolfgang R SperrDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Austria.
Klaus Geissler5Medical Department for Hematology and Oncology, Hospital Hietzing, Vienna, Austria.
Jürg SchwallerDepartment of Biomedicine, University Children's Hospital Basel, Switzerland.
Richard MorigglLudwig Boltzmann Institute for Cancer Research, Vienna, Austria.
Marie C BénéHematology Biology, University Hospital, Nantes, France.
Ulrich JägerDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Austria.
Hans-Peter HornyInstitute of Pathology, Ludwig-Maximilian University, Munich, Germany.
Olivier HermineImagine Institute, INSERM U 1163, CNRS 8654, Université Paris Descartes, Sorbonne, Paris Cité, France peter.valent@meduniwien.ac.at ohermine@gmail.com.
Ludwig Boltzmann Cluster for Cardiovascular Research · ATInnsbruck Medical University · ATMedical University of Vienna · ATHeinrich Heine University Düsseldorf · DEKlinik Hietzing · ATKrankenhaus der Elisabethinen · ATLudwig Boltzmann Institute for Cancer Research · ATLudwig-Maximilians-Universität München · DEMedizinische Hochschule Hannover · DEParacelsus Medical University · ATSorbonne Paris Cité · FRUniversity Children’s Hospital Basel · CHUniversity of Veterinary Medicine Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological erythropoiesis with consequent anemia is a leading cause of symptomatic morbidity in internal medicine. The etiologies of anemia are complex and include reactive as well as neoplastic conditions. Clonal expansion of erythroid cells in the bone marrow may result in peripheral erythrocytosis and polycythemia but can also result in anemia when clonal cells are dysplastic and have a maturation arrest that leads to apoptosis and hinders migration, a constellation typically seen in the myelodysplastic syndromes. Rarely, clonal expansion of immature erythroid blasts results in a clinical picture resembling erythroid leukemia. Although several mechanisms underlying normal and abnormal erythropoiesis and the pathogenesis of related disorders have been deciphered in recent years, little is known about specific markers and targets through which prognosis and therapy could be improved in anemic or polycythemic patients. In order to discuss new markers, targets and novel therapeutic approaches in erythroid disorders and the related pathologies, a workshop was organized in Vienna in April 2017. The outcomes of this workshop are summarized in this review, which includes a discussion of new diagnostic and prognostic markers, the updated WHO classification, and an overview of new drugs used to stimulate or to interfere with erythropoiesis in various neoplastic and reactive conditions. The use and usefulness of established and novel erythropoiesis-stimulating agents for various indications, including myelodysplastic syndromes and other neoplasms, are also discussed.

Indexed as

ErythropoiesisGene Expression Regulation, NeoplasticAdultAnemiaErythroid CellsHumansNeoplasmsPolycythemia

Identifiers

PMID30076180
PMCPMC6165792
OpenAlexW2886141713

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.