Genetic Variants in C-Reactive Protein and Ischemic Stroke Susceptibility

Considerable discrepancies in the previously reported associations of the C-reactive protein (CRP) gene variants and ischemic stroke (IS) risk prompted us to per- form this meta-analysis. We selected the fixed effects Mantel-Haenszel method to estimate the risk of IS (OR (odds ratio) along with its 95 % CI (confidence interval)) in relation to the CRP variants (-717 A ( G, 1444 C ( T). Heterogeneity test, influence analysis and publication bias test were appropriately performed using respective meth- ods. We analyzed 1,926 IS patients and 2,678 controls and found the -717 A ( G variant was not significantly associated with overall IS risk. Subsequent analysis of the 1444 C ( T variant involving 3,278 samples similarly revealed no significant association with IS. There was no substantial heterogeneity or publication bias in this ana- lysis. Our meta-analysis may provide first evidence show- ing that genetic variants within the CRP locus are unlikely to modulate risk of IS.