Association between rs1801133 polymorphism and risk of adult ischemic stroke: Meta-analysis based on case-control studies

- rs1801133 polymorphism is associated with increased risk of ischemic stroke.
- A significant strength between T allele and stroke is in Asian, Caucasian, male, and young-middle populations.
- The risk of ischemic stroke for rs1801133 polymorphism is different in sex.

BackgroundThis study is aimed to quantify the strength of the association between rs1801133 polymorphism and ischemic stroke risk.MethodsWe have searched Medline, Springer, and Embase for studies investigating the association between rs1801133 polymorphism and ischemic stroke risk. We estimated the pooled odds ratio with its 95% confidence intervals to assess this possible association.ResultsForty case-control studies comprising 8809 cases and 9130 controls are eligible for this meta-analysis on the basis of relation of rs1801133 polymorphism to ischemic stroke risk. Hardy-Weinberg equilibrium was used to perform in controls for excluding articles. The overall analysis suggested that rs1801133 polymorphism was associated with increased risk of ischemic stroke (ORT versus C = 1.16, 95% CI 1.10-1.22; ORTT versus TC + CC = 1.32, 95% CI 1.18-1.47; ORTT + TC versus CC = 1.11, 95% CI 1.04-1.18). Subgroup analysis showed that T allele was a significant strength between T allele and stroke risk in Asian, Caucasian, male and young-middle populations (OR = 1.19, 1.11, 1.30, 1.16, respectively). Compared with TC + CC, TT genotype was found to be a risk factor for developing ischemic stroke in Asian, Caucasian and male (OR = 1.41, 1.20, 1.77, respectively). Additionally, TT + TC retained a significant increase for ischemic stroke only in Asian comparable to CC genotype (OR = 1.14).ConclusionsThe rs1801133 polymorphism could be capable of increasing ischemic stroke susceptibility in Asian, male and young-middle populations.