Apolipoprotein E Genotype Is Associated With CT Angiography Spot Sign in Lobar Intracerebral Hemorrhage

作者：Brouwers H Bart^*; Biffi Alessandro; McNamara Kristen A; Ayres Alison M; Valant Valerie; Schwab Kristin; Romero Javier M; Viswanathan Anand; Greenberg Steven M; Rosand Jonathan; Goldstein Joshua N

来源：Stroke, 2012, 43(8): 2120-2125.

DOI：10.1161/STROKEAHA.112.659094

• APOE
• CTA spot sign
• genetics
• hematoma expansion
• intracerebral hemorrhage

Background and Purpose-The CT angiography (CTA) spot sign predicts hematoma expansion and poor outcome in patients with primary intracerebral hemorrhage (ICH). The biological underpinnings of the spot sign remain poorly understood; it may be that the underlying vasculopathy influences its presence. Therefore, we conducted a study to identify genetic predictors of the spot sign.
Methods-In an ongoing prospective cohort study, we analyzed 371 patients with CTA and genetic data available. CTAs were reviewed for the spot sign by 2 experienced readers, blinded to clinical data, according to validated criteria. Analyses were stratified by ICH location.
Results-In multivariate analysis, patients on warfarin were more likely to have a spot sign regardless of ICH location (OR, 3.85; 95% CI, 1.33-11.13 in deep ICH and OR, 2.86; 95% CI, 1.33-6.13 in lobar ICH). Apolipoprotein E epsilon 2, but not epsilon 4, was associated with the presence of a spot sign in lobar ICH (OR, 2.09; 95% CI, 1.05-4.19). There was no effect for epsilon 2 or epsilon 4 in deep ICH.
Conclusions-Patients with ICH on warfarin are more likely to present with a spot sign regardless of ICH location. Among patients with lobar ICH, those who possess the apolipoprotein E epsilon 2 allele are more likely to have a spot sign. Given the established relationship between apolipoprotein E epsilon 2 and vasculopathic changes in cerebral amyloid angiopathy, our findings suggest that both hemostatic factors and vessel pathology influence spot sign presence. (Stroke. 2012;43:2120-2125.)

• 出版日期2012-8