Back to Search Start Over

Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age.

Authors :
Ostrom QT
Kinnersley B
Armstrong G
Rice T
Chen Y
Wiencke JK
McCoy LS
Hansen HM
Amos CI
Bernstein JL
Claus EB
Eckel-Passow JE
Il'yasova D
Johansen C
Lachance DH
Lai RK
Merrell RT
Olson SH
Sadetzki S
Schildkraut JM
Shete S
Rubin JB
Andersson U
Rajaraman P
Chanock SJ
Linet MS
Wang Z
Yeager M
Houlston RS
Jenkins RB
Wrensch MR
Melin B
Bondy ML
Barnholtz-Sloan JS
Source :
International journal of cancer [Int J Cancer] 2018 Nov 15; Vol. 143 (10), pp. 2359-2366. Date of Electronic Publication: 2018 Sep 19.
Publication Year :
2018

Abstract

Glioblastoma (GBM) is the most common malignant brain tumor in the United States. Incidence of GBM increases with age, and younger age-at-diagnosis is significantly associated with improved prognosis. While the relationship between candidate GBM risk SNPs and age-at-diagnosis has been explored, genome-wide association studies (GWAS) have not previously been stratified by age. Potential age-specific genetic effects were assessed in autosomal SNPs for GBM patients using data from four previous GWAS. Using age distribution tertiles (18-53, 54-64, 65+) datasets were analyzed using age-stratified logistic regression to generate p values, odds ratios (OR), and 95% confidence intervals (95%CI), and then combined using meta-analysis. There were 4,512 total GBM cases, and 10,582 controls used for analysis. Significant associations were detected at two previously identified SNPs in 7p11.2 (rs723527 [p <subscript>54-63</subscript> = 1.50x10 <superscript>-9</superscript> , OR <subscript>54-63</subscript> = 1.28, 95%CI <subscript>54-63</subscript> = 1.18-1.39; p <subscript>64+</subscript> = 2.14x10 <superscript>-11</superscript> , OR <subscript>64+</subscript> = 1.32, 95%CI <subscript>64+</subscript> = 1.21-1.43] and rs11979158 [p <subscript>54-63</subscript> = 6.13x10 <superscript>-8</superscript> , OR <subscript>54-63</subscript> = 1.35, 95%CI <subscript>54-63</subscript> = 1.21-1.50; p <subscript>64+</subscript> = 2.18x10 <superscript>-10</superscript> , OR <subscript>64+</subscript> = 1.42, 95%CI <subscript>64+</subscript> = 1.27-1.58]) but only in persons >54. There was also a significant association at the previously identified lower grade glioma (LGG) risk locus at 8q24.21 (rs55705857) in persons ages 18-53 (p <subscript>18-53</subscript> = 9.30 × 10 <superscript>-11</superscript> , OR <subscript>18-53</subscript> = 1.76, 95%CI <subscript>18-53</subscript> = 1.49-2.10). Within The Cancer Genome Atlas (TCGA) there was higher prevalence of 'LGG'-like tumor characteristics in GBM samples in those 18-53, with IDH1/2 mutation frequency of 15%, as compared to 2.1% [54-63] and 0.8% [64+] (p = 0.0005). Age-specific differences in cancer susceptibility can provide important clues to etiology. The association of a SNP known to confer risk for IDH1/2 mutant glioma and higher prevalence of IDH1/2 mutation within younger individuals 18-53 suggests that more younger individuals may present initially with 'secondary glioblastoma.'<br /> (© 2018 UICC.)

Details

Language :
English
ISSN :
1097-0215
Volume :
143
Issue :
10
Database :
MEDLINE
Journal :
International journal of cancer
Publication Type :
Academic Journal
Accession number :
30152087
Full Text :
https://doi.org/10.1002/ijc.31759