High frequency of apolipoprotein E epsilon 2 allele in hemorrhage due to cerebral amyloid angiopathy

被引:242
作者
Nicoll, JAR
Burnett, C
Love, S
Graham, DI
Dewar, D
Ironside, JW
Stewart, J
Vinters, HV
机构
[1] UNIV GLASGOW,DEPT NEUROPATHOL,GLASGOW,LANARK,SCOTLAND
[2] UNIV GLASGOW,WELLCOME SURG INST,GLASGOW,LANARK,SCOTLAND
[3] FRENCHAY HOSP,DEPT NEUROPATHOL,BRISTOL BS16 1LE,AVON,ENGLAND
[4] WESTERN GEN HOSP,DEPT NEUROPATHOL,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
[5] UNIV CALIF LOS ANGELES,MED CTR,DEPT PATHOL & LAB MED NEUROPATHOL,LOS ANGELES,CA 90024
关键词
D O I
10.1002/ana.410410607
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 hemorrhage independently of its association with concomitant Alzheimer's disease (AD). We determined the apoE genotypes of 36 patients presenting with cerebral hemorrhage associated with histologically confirmed CAA. The frequency of apoE epsilon 2 was 0.25 and the frequency of apoE epsilon 4 was 0.18. Patients with CAA-related hemorrhage and concomitant AD pathology (CERAD criteria, n = 17) had a high apoE epsilon 4 frequency, close to that in AD cases without hemorrhage. Patients in whom CAA-related hemorrhage occurred in the absence of significant AD pathology (n = 13) had an apoE epsilon 4 frequency somewhat lower than non-AD controls without hemorrhage. However, in CAA-related hemorrhage, the apoE epsilon 2 frequency was high regardless of whether significant AD pathology was present. We conclude that whereas possession of apoE 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 independent risk factor for CAA-related hemorrhage.
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收藏
页码:716 / 721
页数:6
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