Jar. Nicoll et al., HIGH-FREQUENCY OF APOLIPOPROTEIN-E EPSILON-2 ALLELE IN HEMORRHAGE DUETO CEREBRAL AMYLOID ANGIOPATHY, Annals of neurology, 41(6), 1997, pp. 716-721
From the somewhat conflicting published data on apolipoprotein E (apoE
) genotype in hemorrhage due to cerebral amyloid angiopathy (CAA), it
is unclear whether apoE genotype influences the risk of CAA-related he
morrhage independently of its association with concomitant Alzheimer's
disease (AD). We determined the apoE genotypes of 36 patients present
ing with cerebral hemorrhage associated with histologically confirmed
CAA. The frequency of apoE epsilon 2 was 0.25 and the frequency of apo
E epsilon 4 was 0.18. Patients with CAA-related hemorrhage and concomi
tant AD pathology (CERAD criteria, n = 17) had a high apoE epsilon 4 f
requency, close to that in AD cases without hemorrhage. Patients in wh
om CAA-related hemorrhage occurred in the absence of significant AD pa
thology (n = 13) had an apoE epsilon 4 frequency somewhat lower than n
on-AD controls without hemorrhage. However, in CAA-related hemorrhage,
the apoE epsilon 2 frequency was high regardless of whether significa
nt AD pathology was present. We conclude that whereas possession of ap
oE epsilon 2 may be a risk factor for cerebral hemorrhage due to CAA,
apoE epsilon 4 is a risk factor for concomitant AD but not an independ
ent risk factor for CAA-related hemorrhage.