Evidence map›Paper›PMID 32873778›Full record

ArticleBlood cancer journal2020

Genetic polymorphisms associated with telomere length and risk of developing myeloproliferative neoplasms.

Matteo Giaccherini, Angelica Macauda, Nicola Sgherza, Juan Sainz, Federica Gemignani, Josè Manuel Sanchez Maldonado, Manuel Jurado, Francesca Tavano, Grzegorz Mazur, Andrés Jerez and 9 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Risk factors for clonal hematopoiesis of indeterminate potential and mosaic chromosomal alterations.Translational research : the journal of laboratory and clinical medicine · 2023
    Review
  9. Article
  10. Parental telomeres implications on immune senescence of newborns.American journal of clinical and experimental immunology · 2023
    Article
  11. Article
  12. Article
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  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Telomere Length and Male Fertility.International journal of molecular sciences · 2021
    Article
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 10 institutions in 5 countries.

Matteo GiaccheriniDepartment of Biology, University of Pisa, Pisa, Italy.ORCID http://orcid.org/0000-0002-0363-6632
Angelica MacaudaDepartment of Biology, University of Pisa, Pisa, Italy.
Nicola SgherzaDivision of Hematology, Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.ORCID http://orcid.org/0000-0001-5447-1068
Juan SainzGenomic Oncology Area, GENYO, Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.ORCID http://orcid.org/0000-0002-9355-2423
Federica GemignaniDepartment of Biology, University of Pisa, Pisa, Italy.
Josè Manuel Sanchez MaldonadoGenomic Oncology Area, GENYO, Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
Manuel JuradoGenomic Oncology Area, GENYO, Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government, PTS Granada, Granada, Spain.
Francesca TavanoDivision of Gastroenterology and Research Laboratory, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Grzegorz MazurDepartment of Internal Medicine, Occupational Diseases, Hypertension and Clinical Oncology, Wroclaw Medical University, Wroclaw, Poland.
Andrés JerezHematology and Medical Oncology Department, University Hospital Morales Meseguer-IMIB, CIBERER, Murcia, Spain.
Joanna Góra-TyborDepartment of Hematology, Medical University of Łódź, Łódź, Poland.
Aleksandra GołosDepartment of Clinical Oncology and Chemotherapy, Magodent Hospital, Warsaw, Poland.ORCID http://orcid.org/0000-0002-7780-3587
Francisca Hernández MohedoMonoclonal Gammopathies Unit, University Hospital Virgen de las Nieves, Granada, Spain.
Joaquin Martinez LopezHospital 12 de Octubre, H12O-CNIO Hematological Malignancies Clinical Research Unitc Compluntense University, CIBERONC, Madrid, Spain.ORCID http://orcid.org/0000-0001-7908-0063
Judit VárkonyiThird Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
Raffaele SpadanoDivision of Hematology, Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Aleksandra ButrymDepartment of Cancer Prevention and Therapy, Wroclaw Medical University, Wroclaw, Poland.
Federico Canzian *Genomic Epidemiology Group, German Cancer Research Center (DKFZ), Heidelberg, Germany. f.canzian@dkfz.de.ORCID http://orcid.org/0000-0002-4261-4583
Daniele Campa *Department of Biology, University of Pisa, Pisa, Italy.
University of Pisa · ITCasa Sollievo della Sofferenza · ITInstituto de Investigación Biosanitaria de Granada · ESWroclaw Medical University · PLCentro de Investigación Biomédica en Red de Cáncer · ESGerman Cancer Research Center · DEHospital General Universitario Morales Meseguer · ESMedical University of Lodz · PLSemmelweis University · HUUniversidad de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomere length measured in leukocyte (LTL) has been found to be associated with the risk of developing several cancer types, including myeloproliferative neoplasms (MPNs). LTL is genetically determined by, at least, 11 SNPs previously shown to influence LTL. Their combination in a score has been used as a genetic instrument to measure LTL and evaluate the causative association between LTL and the risk of several cancer types. We tested, for the first time, the "teloscore" in 480 MPN patients and 909 healthy controls in a European multi-center case-control study. We found an increased risk to develop MPNs with longer genetically determined telomeres (OR = 1.82, 95% CI 1.24-2.68, P = 2.21 × 10

Indexed as

Polymorphism, Single NucleotideTelomere HomeostasisAgedFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedMyeloproliferative DisordersRisk Factors

Identifiers

PMID32873778
PMCPMC7463014
OpenAlexW3081785837

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.