Evidence map›Paper›PMID 32211575›Full record

ArticleResearch and practice in thrombosis and haemostasis2020

Increased von Willebrand factor levels in polycythemia vera and phenotypic differences with essential thrombocythemia.

Monica Sacco, Paola Ranalli, Stefano Lancellotti, Giovanna Petrucci, Alfredo Dragani, Bianca Rocca, Raimondo De Cristofaro

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

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

  1. Pooled it
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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

7 authors at 4 institutions in 1 country.

Monica SaccoServizio Malattie Emorragiche e Trombotiche Fondazione Policlinico Universitario "A. Gemelli" IRCCS Roma Italy.
Paola RanalliDipartimento di Medicina Interna e Chirurgia Traslazionale Facoltà di Medicina e Chirurgia "A. Gemelli" Università Cattolica del Sacro Cuore Roma Italy.
Stefano LancellottiDipartimento di Ematologia Ospedale S. Spirito Pescara Italy.
Giovanna PetrucciIstituto di Farmacologia Facoltà di Medicina e Chirurgia "A. Gemelli" Università Cattolica del S. Cuore and Fondazione Policlinico Universitario "A. Gemelli" IRCCS Rome Italy.
Alfredo DraganiDipartimento di Medicina Interna e Chirurgia Traslazionale Facoltà di Medicina e Chirurgia "A. Gemelli" Università Cattolica del Sacro Cuore Roma Italy.
Bianca RoccaIstituto di Farmacologia Facoltà di Medicina e Chirurgia "A. Gemelli" Università Cattolica del S. Cuore and Fondazione Policlinico Universitario "A. Gemelli" IRCCS Rome Italy.
Raimondo De CristofaroServizio Malattie Emorragiche e Trombotiche Fondazione Policlinico Universitario "A. Gemelli" IRCCS Roma Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITUniversità Cattolica del Sacro Cuore · ITAgostino Gemelli University Polyclinic · ITOspedale di Santo Spirito · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcquired von Willebrand factor (VWF) deficiency was described in Philadelphia-negative myeloproliferative neoplasms, especially in essential thrombocythemia (ET). VWF phenotype in contemporary patients with polycythemia vera (PV) remains less explored.

objectivesTo characterize the VWF phenotype in PV and to compare VWF phenotype in PV with matched healthy subjects and ET patients. PATIENTS/

methodsWe studied 48 PV patients, treated according to current recommendations (hematocrit ≤ 45%, on low-dose aspirin prophylaxis); 48 healthy and 41 subjects with ET, all sex, age, and blood group matched. We measured VWF antigen, activity, multimeric pattern, ADAMTS-13, and factor VIII (FVIII) antigen.

resultsIn patients with PV, VWF antigen and activity were significantly higher than in healthy subjects (antigen: 119[96-137] vs 93[79-107] IU/dL; activity: 114[95-128] vs 90[79-107] IU/dL, respectively, medians and interquartile,

conclusionsPatients with PV show increased VWF and FVIII levels, predicted by JAK2-p.V617F burden and erythrocyte count. At variance with ET, acquired VWF defect was not observed in PV. High VWF/FVIII levels may sustain the thrombotic diathesis of PV and may be investigated as biomarkers for risk stratification.

Indexed as

essential thrombocythemiafactor VIIImyeloproliferative neoplasmspolycythemia veravon Willebrand factor

Identifiers

PMID32211575
PMCPMC7086469
OpenAlexW3007052876

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.