The association between longer relative leukocyte telomere length and risk of glioma is independent of the potentially confounding factors allergy, BMI, and smoking.


Journal

Cancer causes & control : CCC
ISSN: 1573-7225
Titre abrégé: Cancer Causes Control
Pays: Netherlands
ID NLM: 9100846

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 03 07 2018
accepted: 06 12 2018
pubmed: 19 12 2018
medline: 4 4 2019
entrez: 19 12 2018
Statut: ppublish

Résumé

Previous studies have suggested an association between relative leukocyte telomere length (rLTL) and glioma risk. This association may be influenced by several factors, including allergies, BMI, and smoking. Previous studies have shown that individuals with asthma and allergy have shortened relative telomere length, and decreased risk of glioma. Though, the details and the interplay between rLTL, asthma and allergies, and glioma molecular phenotype is largely unknown. rLTL was measured by qPCR in a Swedish population-based glioma case-control cohort (421 cases and 671 controls). rLTL was related to glioma risk and health parameters associated with asthma and allergy, as well as molecular events in glioma including IDH1 mutation, 1p/19q co-deletion, and EGFR amplification. Longer rLTL was associated with increased risk of glioma (OR = 1.16; 95% CI 1.02-1.31). Similar to previous reports, there was an inverse association between allergy and glioma risk. Specific, allergy symptoms including watery eyes was most strongly associated with glioma risk. High body mass index (BMI) a year prior diagnosis was significantly protective against glioma in our population. Adjusting for allergy, asthma, BMI, and smoking did not markedly change the association between longer rLTL and glioma risk. rLTL among cases was not associated with IDH1 mutation, 1p/19q co-deletion, or EGFR amplification, after adjusting for age at diagnosis and sex. In this Swedish glioma case-control cohort, we identified that long rLTL increases the risk of glioma, an association not confounded by allergy, BMI, or smoking. This highlights the complex interplay of the immune system, rLTL and cancer risk.

Identifiants

pubmed: 30560391
doi: 10.1007/s10552-018-1120-2
pii: 10.1007/s10552-018-1120-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

177-185

Subventions

Organisme : NCI NIH HHS
ID : R01 CA119215
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA139020
Pays : United States
Organisme : National Cancer Institute NIH
ID : 5R01CA119215, 5R01CA139020

Auteurs

Ulrika Andersson (U)

Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden. ulrika.l.andersson@umu.se.

Sofie Degerman (S)

Department of Medical Biosciences, Pathology, Umea University, Umea, Sweden.

Anna M Dahlin (AM)

Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden.

Carl Wibom (C)

Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden.

Gunnar Johansson (G)

Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden.

Melissa L Bondy (ML)

Department of Medicine, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.

Beatrice S Melin (BS)

Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden.

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Classifications MeSH