ASSOCIATION OF TUMOR NECROSIS FACTOR-α–238G>A AND APOLIPOPROTEIN E2 POLYMORPHISMS WITH INTRACRANIAL HEMORRHAGE AFTER BRAIN ARTERIOVENOUS MALFORMATION TREATMENT

Abstract

Abstract OBJECTIVE We previously reported specific genotypes of polymorphisms in two genes, tumor necrosis factor-α (TNF-α-238G > A) and Apolipoprotein E (ApoE e2), as independent predictors of new intracranial hemorrhage (ICH) in the natural course of untreated brain arteriovenous malformations. We hypothesized that the risk of posttreatment ICH would also be greater in patients with brain arteriovenous malformations with these genotypes. METHODS Two hundred fifteen patients undergoing brain arteriovenous malformation treatment (embolization, arteriovenous malformation resection, radiosurgery, or any combination of these) were genotyped and followed longitudinally. Association of genotype with new symptomatic ICH after initiation of treatment was assessed using Cox proportional hazards adjusted for treatment type, demographics, and established ICH risk factors censored at the time of the last follow-up evaluation or death. RESULTS The cohort was 48% male and 55% Caucasian, and 52% had an ICH before the initiation of treatment; the mean age ± standard deviation was 36.6 ± 17.2 years. Posttreatment ICH occurred in 34 (16%) patients with a median follow-up period of 1.9 years (interquartile range, 1.6 yr). After adjustment, the risk of posttreatment ICH was greater for TNF-α-238 AG genotype (hazard ratio [HR], 3.5; 95% confidence interval [CI], 1.3–9.8; P = 0.016) and ApoE e2 (HR, 3.2; 95% CI, 1.0–9.7; P = 0.042). Similar trends for the TNF-α-238 AG genotype were seen in surgery (HR, 4.2; 95% CI, 0.6–28.8; P = 0.14) and radiosurgery subsets (HR, 3.8; 95% CI, 0.7–19.4; P = 0.11). An effect of ApoE e2 was seen in radiosurgery subsets (HR, 10.9; 95% CI, 1.3–93.7; P = 0.030), but not in surgery subsets (HR, 1.4; 95% CI, 0.3–7.4; P = 0.67). CONCLUSION Despite a variety of different mechanisms for posttreatment hemorrhage, these data suggest that the TNF-α and ApoE genotypes may contribute common phenotypes of enhanced vascular instability that increase the risk of hemorrhagic outcome.