The rs498872 polymorphism is associated with an elevated susceptibility to glioma: a meta-analysis of 36,264 subjects.

Abstract:

:Several genome-wide association studies have already explored the associations between rs498872 polymorphism and glioma, but the results of these studies were not consistent. Consequently, we conducted a meta-analysis of relevant studies to better analyze the effects of rs498872 polymorphism on individual susceptibility to glioma. PubMed, Web of Science and Embase were searched for eligible studies. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated. Totally, 12 studies with 36,264 subjects were analyzed. A significant association with glioma was observed for the rs498872 polymorphism in CC versus CT + TT (dominant comparison, p < 0.0001, OR = 0.81, 95% CI 0.76-0.85), TT versus CC + CT (recessive comparison, p < 0.0001, OR = 1.23, 95% CI 1.13-1.34), CT versus CC + TT (overdominant comparison, p < 0.0001, OR = 1.15, 95% CI 1.09-1.21) and C versus T (allele comparison, p < 0.0001, OR = 0.86, 95% CI 0.84-0.90). Further subgroup analyses yielded similar positive results in both Asians and Caucasians. Our findings suggested that the rs498872 polymorphism may serve as a potential genetic biomarker of glioma in both Asians and Caucasians.

journal_name

Acta Neurol Belg

journal_title

Acta neurologica Belgica

authors

Chen B,Li Y,Chen L,Du Y

doi

10.1007/s13760-019-01081-y

subject

Has Abstract

pub_date

2019-06-01 00:00:00

pages

239-243

issue

2

eissn

0300-9009

issn

2240-2993

pii

10.1007/s13760-019-01081-y

journal_volume

119

pub_type

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