Evidence map›Paper›PMID 35775283›Full record

ArticleCancer medicine2023

Clinical features of acquired erythrocytosis: Low levels of serum erythropoietin in a subset of non-neoplastic erythrocytosis patients.

Yosuke Mori, Marito Araki, Soji Morishita, Misa Imai, Yoko Edahiro, Masafumi Ito, Tomonori Ochiai, Shuichi Shirane, Yoshinori Hashimoto, Hajime Yasuda and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Diagnosis- and Prognosis-Related Gene Alterations inInternational journal of molecular sciences · 2023
    Review
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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

13 authors at 2 institutions in 1 country.

Yosuke MoriDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Marito ArakiLaboratory for the Development of Therapies Against MPN, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-3502-5000
Soji MorishitaLaboratory for the Development of Therapies Against MPN, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0003-1081-0130
Misa ImaiLaboratory for the Development of Therapies Against MPN, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-5192-5957
Yoko EdahiroDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-8386-1871
Masafumi ItoDepartment of Pathology, Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital, Nagoya, Japan.
Tomonori OchiaiDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0001-6156-4211
Shuichi ShiraneDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yoshinori HashimotoDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-3374-9814
Hajime YasudaDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0002-2896-7737
Jun AndoDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Miki AndoDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Norio KomatsuDepartment of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID 0000-0003-1880-9126
Juntendo University · JPJapanese Red Cross Nagoya Daiichi Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcquired erythrocytosis can be classified into polycythemia vera (PV) and non-neoplastic erythrocytosis (NNE). The vast majority of PV patients harbor JAK2 mutations, but differentiating JAK2 mutation-negative PV from NNE is challenging due to a lack of definitive molecular markers.

methodsWe studied the clinical features of 121 patients with erythrocytosis of which 47 (38.8%) were JAK2 mutation-positive and also fulfilled the diagnostic criteria for PV, and 67 (55.4%) JAK2 mutation-negative erythrocytosis patients who were diagnosed as NNE. Diagnosis was strictly based on driver mutation analysis and central pathology review.

resultsNo JAK2 mutation-negative PV patients were found in our cohort. The NNE group showed significantly younger (p < 0.01) age with higher frequency of smoking (p < 0.001), alcohol consumption (p < 0.001), and diabetes mellitus (p < 0.05), whereas the PV group (n = 47) showed significantly higher white blood cell count, platelet count, and lactate dehydrogenase (p < 0.001). Although serum erythropoietin (EPO) levels were significantly higher in NNE compared to PV (p < 0.001), approximately 40% of the NNE patients had EPO levels below the lower range of normal, fulfilling a minor diagnostic criterion of PV and raising the possibility of PV misdiagnosis.

conclusionLow EPO levels in JAK2 mutation-negative erythrocytosis may not be a reliable diagnostic criterion for distinguishing PV from NNE.

Indexed as

ErythropoietinPolycythemiaPolycythemia VeraBiomarkersHumansMutationBiomarkersErythropoietindrinking habiterythrocytosiserythropoietinJAK2lifestyle-related diseasemyeloproliferative neoplasms

Identifiers

PMID35775283
PMCPMC9883404
OpenAlexW4283748651

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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.