Evidence map›Paper›PMID 27579896›Full record

ArticlePloS one2016

A 7-Gene Signature Depicts the Biochemical Profile of Early Prefibrotic Myelofibrosis.

Vibe Skov, Mark Burton, Mads Thomassen, Thomas Stauffer Larsen, Caroline H Riley, Ann Brinch Madelung, Lasse Kjær, Henrik Bondo, Inger Stamp, Mats Ehinger and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. Article
  5. Gene Expression Dysregulation in Whole Blood of Patients withInternational journal of molecular sciences · 2024
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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

18 authors at 7 institutions in 3 countries.

Vibe SkovDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Mark BurtonDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Mads ThomassenDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Thomas Stauffer LarsenDepartment of Hematology X, Odense University Hospital, Odense, Denmark.
Caroline H RileyDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Ann Brinch MadelungDepartment of Pathology, Naestved Hospital, Naestved, Denmark.
Lasse KjærDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Henrik BondoDepartment of Pathology, Naestved Hospital, Naestved, Denmark.
Inger StampDepartment of Pathology, Naestved Hospital, Naestved, Denmark.
Mats EhingerDepartment of Pathology, Lund University Hospital, Lund, Sweden.
Rasmus Dahl-SørensenDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Nana BrochmannDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Karsten NielsenDepartment of Pathology, University of Aarhus, Aarhus, Denmark.
Jürgen ThieleInstitute of Pathology, University of Cologne, Köln, Germany.
Morten K JensenDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Ole Weis BjerrumDepartment of Hematology L, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Torben A KruseDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Hans Carl HasselbalchDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Zealand University Hospital · DKOdense University Hospital · DKNæstved Sygehus · DKAarhus University · DKLund University · SEUniversity of Cologne · DEUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have shown that a large proportion of patients classified as essential thrombocythemia (ET) actually have early primary prefibrotic myelofibrosis (prePMF), which implies an inferior prognosis as compared to patients being diagnosed with so-called genuine or true ET. According to the World Health Organization (WHO) 2008 classification, bone marrow histology is a major component in the distinction between these disease entities. However, the differential diagnosis between them may be challenging and several studies have not been able to distinguish between them. Most lately, it has been argued that simple blood tests, including the leukocyte count and plasma lactate dehydrogenase (LDH) may be useful tools to separate genuine ET from prePMF, the latter disease entity more often being featured by anemia, leukocytosis and elevated LDH. Whole blood gene expression profiling was performed in 17 and 9 patients diagnosed with ET and PMF, respectively. Using elevated LDH obtained at the time of diagnosis as a marker of prePMF, a 7-gene signature was identified which correctly predicted the prePMF group with a sensitivity of 100% and a specificity of 89%. The 7 genes included MPO, CEACAM8, CRISP3, MS4A3, CEACAM6, HEMGN, and MMP8, which are genes known to be involved in inflammation, cell adhesion, differentiation and proliferation. Evaluation of bone marrow biopsies and the 7-gene signature showed a concordance rate of 71%, 79%, 62%, and 38%. Our 7-gene signature may be a useful tool to differentiate between genuine ET and prePMF but needs to be validated in a larger cohort of "ET" patients.

Indexed as

Gene Expression RegulationAdultAgedAged, 80 and overBiopsyBone MarrowFemaleGene Expression ProfilingHumansMaleMiddle AgedPrimary Myelofibrosis

Identifiers

PMID27579896
PMCPMC5007012
OpenAlexW2515516989

What OpenQuestion holds

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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.