ID
45570
Description
Principal Investigator: Preetha Rajaraman, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA MeSH: Glioma https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000652 We conducted a new independent GWAS of adult glioma using 1,856 cases and 4,955 controls from 14 cohort studies belonging to the Cohort Consortium, 3 case-control studies, and 1 population-based case only study. Cases were newly diagnosed glioma [ICDO-3 codes 9380-9480 or equivalent], and controls were cancer-free at the time of glioma diagnosis. We found evidence of strong replication for three of the seven previously reported associations at 20q13.33 (RTEL), 5p15.33 (TERT), and 9p21.3 (CDKN2BAS), and consistent association signals for the remaining four at 7p11.2 (EGFR both loci), 8q24.21 (CCDC26) and 11q23.3 (PHLDB1). The direction and magnitude of the signal were consistent for samples from cohort and case-control studies, but the strength of the association was more pronounced for loci rs6010620 (20q,13.33; RTEL) and rs2736100 (5p15.33, TERT) in cohort studies despite the smaller number of cases in this group, likely due to higher grade tumors being captured in the cohort studies. Our findings suggest that larger studies focusing on novel approaches as well as specific tumor subtypes or subgroups will be required to identify additional common susceptibility loci for glioma risk.
Lien
Mots-clés
Versions (1)
- 23/01/2023 23/01/2023 - Dr. Christian Niklas
Détendeur de droits
Preetha Rajaraman, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA
Téléchargé le
23 janvier 2023
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
dbGaP phs000652 Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent groups, and affection status of samples obtained from adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
- Subject ID, sample ID, and sample use variable obtained from adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
- Subject ID, case or control status of participant, sex, age, and study design of adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
- Sample ID, body site where sample was collected, analyte type [DNA], and tumor status of samples obtained from adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent groups, and affection status of samples obtained from adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
- Subject ID, sample ID, and sample use variable obtained from adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
- Subject ID, case or control status of participant, sex, age, and study design of adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
- Sample ID, body site where sample was collected, analyte type [DNA], and tumor status of samples obtained from adult participants with or without glioma and involved in the "Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)" project.
C0680251 (UMLS CUI [1,2])
C0017638 (UMLS CUI [1,2])
C0332296 (UMLS CUI [2,1])
C0006826 (UMLS CUI [2,2])
C0009932 (UMLS CUI [2,3])