Evidence map›Paper›PMID 27456001›Full record

ArticleOrphanet journal of rare diseases2016

Increased red cell distribution width in Fanconi anemia: a novel marker of stress erythropoiesis.

Rosa Sousa, Cristina Gonçalves, Isabel Couto Guerra, Emília Costa, Ana Fernandes, Maria do Bom Sucesso, Joana Azevedo, Alfredo Rodriguez, Rocio Rius, Carlos Seabra and 9 more

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2016. 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
1.0field-weighted citation impact, top 23% 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, 29 citations in OpenAlex.

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  17. Red blood cell distribution width and ischaemic stroke.Stroke and vascular neurology · 2017
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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

19 authors at 4 institutions in 1 country.

Rosa SousaLaboratory of Cytogenetics, Abel Salazar Institute for Biomedical Sciences, University of Porto (ICBAS, UP), Porto, Portugal.
Cristina GonçalvesClinical Hematology Service, Hospital Center of Porto (CHP), Porto, Portugal.
Isabel Couto GuerraPediatric Hematology Unity, Hospital Center of Porto (CHP), Porto, Portugal.
Emília CostaPediatric Hematology Unity, Hospital Center of Porto (CHP), Porto, Portugal.
Ana FernandesPediatric Hematology-Oncology Unity, Hospital Center of S. João, Porto (CHSJ), Porto, Portugal.
Maria do Bom SucessoPediatric Hematology-Oncology Unity, Hospital Center of S. João, Porto (CHSJ), Porto, Portugal.
Joana AzevedoHematology Service, Hospital and University Center of Coimbra (CHUC), Porto, Portugal.
Alfredo RodriguezLaboratory of Cytogenetics, National Institute of Pediatrics, Ciudad de Mexico (INP), Mexico City, Mexico.
Rocio RiusLaboratory of Cytogenetics, National Institute of Pediatrics, Ciudad de Mexico (INP), Mexico City, Mexico.
Carlos SeabraClinical Pathology Service, Infante D. Pedro Hospital, Aveiro (CHBV), Aveiro, Portugal.
Fátima FerreiraHematology Service, Hospital Center of S. João, Porto (CHSJ), Porto, Portugal.
Letícia RibeiroHematology Service, Hospital and University Center of Coimbra (CHUC), Porto, Portugal.
Anabela FerrãoPediatric Service, Hospital Center of Lisboa Norte (CHLN), Lisbon, Portugal.
Sérgio CastedoMedical Genetics and Prenatal Diagnosis Prof Doctor Sérgio Castedo, Porto (GDPN), Porto, Portugal.
Esmeralda CletoPediatric Hematology Unity, Hospital Center of Porto (CHP), Porto, Portugal.
Jorge CoutinhoClinical Hematology Service, Hospital Center of Porto (CHP), Porto, Portugal.
Félix CarvalhoUCIBIO-REQUIMTE, Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, Porto, Portugal.
José BarbotPediatric Hematology Unity, Hospital Center of Porto (CHP), Porto, Portugal.
Beatriz PortoLaboratory of Cytogenetics, Abel Salazar Institute for Biomedical Sciences, University of Porto (ICBAS, UP), Porto, Portugal. bporto@icbas.up.pt.ORCID 0000-0003-4281-5438
CUF Porto Hospital · PTHospital de São João · PTUniversidade do Porto · PTCentro Hospitalar Lisboa Norte · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRed cell distribution width (RDW), a classical parameter used in the differential diagnosis of anemia, has recently been recognized as a marker of chronic inflammation and high levels of oxidative stress (OS). Fanconi anemia (FA) is a genetic disorder associated to redox imbalance and dysfunctional response to OS. Clinically, it is characterized by progressive bone marrow failure, which remains the primary cause of morbidity and mortality. Macrocytosis and increased fetal hemoglobin, two indicators of bone marrow stress erythropoiesis, are generally the first hematological manifestations to appear in FA. However, the significance of RDW and its possible relation to stress erythropoiesis have never been explored in FA. In the present study we analyzed routine complete blood counts from 34 FA patients and evaluated RDW, correlating with the hematological parameters most consistently associated with the FA phenotype.

resultsWe showed, for the first time, that RDW is significantly increased in FA. We also showed that increased RDW is correlated with thrombocytopenia, neutropenia and, most importantly, highly correlated with anemia. Analyzing sequential hemograms from 3 FA patients with different clinical outcomes, during 10 years follow-up, we confirmed a consistent association between increased RDW and decreased hemoglobin, which supports the postulated importance of RDW in the evaluation of hematological disease progression.

conclusionsThis study shows, for the first time, that RDW is significantly increased in FA, and this increment is correlated with neutropenia, thrombocytopenia, and highly correlated with anemia. According to the present results, it is suggested that increased RDW can be a novel marker of stress erythropoiesis in FA.

Indexed as

AdolescentBiomarkersChildChild, PreschoolCytogeneticsErythrocytesErythropoiesisFanconi AnemiaFemaleHumansMaleOxidative StressBiomarkersBone marrow failure (BMF)Fanconi anemia (FA)Oxidative stress (OS)Red cell distribution width (RDW)Stress erythropoiesis

Identifiers

PMID27456001
PMCPMC4960735
OpenAlexW2476020879

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.