Evidence map›Paper›PMID 31525475›Full record

SynthesisBone2020

Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population.

Chenan Zhang, Helen M Hansen, Eleanor C Semmes, Julio Gonzalez-Maya, Libby Morimoto, Qingyi Wei, William C Eward, Suzanne B DeWitt, Jillian H Hurst, Catherine Metayer and 3 more

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in Bone, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  11. Telomeres and telomerase in Sarcoma disease and therapy.International journal of medical sciences · 2024
    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 5 institutions in 1 country.

Chenan ZhangDepartment of Epidemiology and Biostatistics, University of California, San Francisco, United States.
Helen M HansenDepartment of Neurological Surgery, University of California, San Francisco, United States.
Eleanor C SemmesChildren's Health and Discovery Institute, Department of Pediatrics, Duke University, United States.
Julio Gonzalez-MayaDepartment of Neurological Surgery, University of California, San Francisco, United States.
Libby MorimotoSchool of Public Health, University of California, Berkeley, United States.
Qingyi WeiDepartment of Population Health Sciences, Duke University, United States; Duke Cancer Institute, Duke University, United States.
William C EwardDuke Cancer Institute, Duke University, United States; Department of Orthopaedic Surgery, Duke University, United States.
Suzanne B DeWittDepartment of Pathology, Duke University, United States.
Jillian H HurstChildren's Health and Discovery Institute, Department of Pediatrics, Duke University, United States.
Catherine MetayerSchool of Public Health, University of California, Berkeley, United States.
Adam J de SmithCenter for Genetic Epidemiology, University of Southern California, United States.
Joseph L WiemelsDepartment of Epidemiology and Biostatistics, University of California, San Francisco, United States; Department of Neurosurgery, Duke University, United States.
Kyle M WalshDepartment of Epidemiology and Biostatistics, University of California, San Francisco, United States; Duke Cancer Institute, Duke University, United States; Department of Neurosurgery, Duke University, United States. Electronic address: Kyle.Walsh@Duke.edu.
Duke University · USUniversity of California, San Francisco · USDiscovery Institute · USUniversity of California, Berkeley · USUniversity of Southern California · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Training Program in Translational Brain Tumor ResearchT32CA151022 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2010 to 2026
$6.6M
Genetic Susceptibility to Pediatric Glioma inIndividuals and Diverse populationsR01CA194189 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI WALSH, KYLE M, WIEMELS, JOSEPH LEO · 2015 to 2020
$5.0M
Genome-Wide Association Study of Childhood Leukemia by Hispanic StatusR01CA155461 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MA, XIAOMEI, WIEMELS, JOSEPH LEO · 2011 to 2014
$4.1M
NCCDPHP CDC HHS NU58DP006344NCI NIH HHS HHSN261201800009CNCI NIH HHS HHSN261201800009INCI NIH HHS HHSN261201800015CNCI NIH HHS HHSN261201800015INCI NIH HHS HHSN261201800032CNCI NIH HHS HHSN261201800032INCI NIH HHS R01 CA155461NCI NIH HHS R01 CA194189NCI NIH HHS T32 CA151022NIGMS NIH HHS T32 GM007171
6 · The paper itself

Abstract

Osteosarcoma, a malignant primary bone tumor most commonly diagnosed in children and adolescents, has a poorly understood genetic etiology. Genome-wide association studies (GWAS) and candidate-gene analyses have identified putative risk variants in subjects of European ancestry. However, despite higher incidence among African-American and Hispanic children, little is known regarding common heritable variation that contributes to osteosarcoma incidence and clinical presentation across racial/ethnic groups. In a multi-ethnic sample of non-Hispanic white, Hispanic, African-American and Asian/Pacific Islander children (537 cases, 2165 controls), we performed association analyses assessing previously-reported loci for osteosarcoma risk and metastasis, including meta-analysis across racial/ethnic groups. We also assessed a previously described association between genetic predisposition to longer leukocyte telomere length (LTL) and osteosarcoma risk in this independent multi-ethnic dataset. In our sample, we were unable to replicate previously-reported loci for osteosarcoma risk or metastasis detected in GWAS of European-ancestry individuals in either ethnicity-stratified analyses or meta-analysis across ethnic groups. Our analyses did confirm that genetic predisposition to longer LTL is a risk factor for osteosarcoma (OR

Indexed as

EthnicityOsteosarcomaAdolescentChildGenetic Predisposition to DiseaseGenome-Wide Association StudyHispanic or LatinoHumansPolymorphism, Single NucleotideGenome-wide association studyMendelian randomizationOsteosarcomaPolygenic risk score

Identifiers

PMID31525475
PMCPMC6885126
OpenAlexW2972610082

What OpenQuestion holds

Textmetadata
LicenceTDM
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.