Evidence map›Paper›PMID 27651169›Full record

ArticleHaematologica2016

Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations.

Carme Camps, Nayia Petousi, Celeste Bento, Holger Cario, Richard R Copley, Mary Frances McMullin, Richard van Wijk, Peter J Ratcliffe, Peter A Robbins, Jenny C Taylor and 1 more

Abstract read
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

46 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Trial
  3. Article
  4. Identification and Screening of Lactate-Related Genes as Molecular Markers for Early Diagnosis of Steroid-Induced Osteonecrosis of the Femoral Head.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Article
  6. Impact ofEJHaem · 2024
    Article
  7. Article
  8. Article
  9. Idiopathic erythrocytosis: a germline disease?Clinical and experimental medicine · 2024
    Article
  10. Article
  11. Article
  12. Coexistence of Multiple Gene Variants in Some Patients with Erythrocytoses.Mediterranean journal of hematology and infectious diseases · 2024
    Article
  13. Article
  14. Article
  15. ComprehensiveHaematologica · 2023
    Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Fount, fate, features, and function of renal erythropoietin-producing cells.Pflugers Archiv : European journal of physiology · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Carme CampsNational Institute for Health Research (NIHR) Comprehensive Biomedical Research Centre, Oxford, UK.
Nayia PetousiNuffield Department of Medicine, University of Oxford, UK nayia.petousi@ndm.ox.ac.uk.
Celeste BentoHematology Department, Centro Hospitalar e Universitário de Coimbra, Portugal.
Holger CarioDepartment of Pediatrics and Adolescent Medicine, University Medical Center, Ulm, Germany.
Richard R CopleyNational Institute for Health Research (NIHR) Comprehensive Biomedical Research Centre, Oxford, UK.
Mary Frances McMullinCentre for Cancer Research and Cell Biology, Queen's University, Belfast, UK.
Richard van Wijk
Peter J RatcliffeNuffield Department of Medicine, University of Oxford, UK.
Peter A RobbinsDepartment of Physiology, Anatomy and Genetics, University of Oxford, UK.
Jenny C TaylorNational Institute for Health Research (NIHR) Comprehensive Biomedical Research Centre, Oxford, UK.
WGS500 Consortium

Funding

Medical Research Council G0900747Wellcome TrustWellcome Trust 090532/Z/09/Z
6 · The paper itself

Abstract

Erythrocytosis is a rare disorder characterized by increased red cell mass and elevated hemoglobin concentration and hematocrit. Several genetic variants have been identified as causes for erythrocytosis in genes belonging to different pathways including oxygen sensing, erythropoiesis and oxygen transport. However, despite clinical investigation and screening for these mutations, the cause of disease cannot be found in a considerable number of patients, who are classified as having idiopathic erythrocytosis. In this study, we developed a targeted next-generation sequencing panel encompassing the exonic regions of 21 genes from relevant pathways (~79 Kb) and sequenced 125 patients with idiopathic erythrocytosis. The panel effectively screened 97% of coding regions of these genes, with an average coverage of 450×. It identified 51 different rare variants, all leading to alterations of protein sequence, with 57 out of 125 cases (45.6%) having at least one of these variants. Ten of these were known erythrocytosis-causing variants, which had been missed following existing diagnostic algorithms. Twenty-two were novel variants in erythrocytosis-associated genes (EGLN1, EPAS1, VHL, BPGM, JAK2, SH2B3) and in novel genes included in the panel (e.g. EPO, EGLN2, HIF3A, OS9), some with a high likelihood of functionality, for which future segregation, functional and replication studies will be useful to provide further evidence for causality. The rest were classified as polymorphisms. Overall, these results demonstrate the benefits of using a gene panel rather than existing methods in which focused genetic screening is performed depending on biochemical measurements: the gene panel improves diagnostic accuracy and provides the opportunity for discovery of novel variants.

Indexed as

MutationGenetic VariationHumansMolecular Diagnostic TechniquesPolycythemiaSequence Analysis, DNA

Identifiers

PMID27651169
PMCPMC5394871

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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.