Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa 920-8640, Japan
Address for correspondence: Masahito Yamada, Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, 13-1, Takara-machi, Kanazawa 920-8640, Japan. Voice: +81-76-265-2290; fax: +81-76-234-4253.
m-yamada{at}med.kanazawa-u.ac.jp
Ann. N.Y. Acad. Sci. 977: 37-44 (2002).
To elucidate risk factors for cerebral amyloid angiopathy (CAA)
in the elderly, we have investigated 201 autopsy cases of elderly
Japanese (ages: 62-104 years), including 82 patients with Alzheimer's
disease (AD). Severity of CAA showed no relationship with the
history of hypertension, hyperlipidemia, or diabetes mellitus,
nor with severity of atherosclerosis of cerebral and systemic
arteries, indicating that common vascular risk factors would
not be related to CAA. Incidence and severity of CAA were significantly
higher in the AD cases compared with the non-AD cases (
p <
0.0001). Severity of CAA correlated with densities of senile
plaques and neurofibrillary tangles in total and non-AD cases,
although the correlations were not significant within the AD
cases. Associations of genetic polymorphisms with CAA have been
investigated for genes of apolipoprotein E (
APOE), presenilin
1 (
PS1),

1-antichymotrypsin (
ACT), butyrylcholinesterase,

2-macroglobulin,
and paraoxonase. Severity of CAA in
APOE 
4 carriers is significantly
higher than that in non-

4 carriers in total cases, although
no significant difference was found in the CAA severity between
the

4 carriers and non-

4 carriers within the AD or non-AD group.
An intronic polymorphism of
PS1 was significantly associated
with the severity of CAA, indicating that the
PS1 2/2 genotype
may be related to lower risk of CAA. A polymorphism in the signal
peptide sequence of
ACT was significantly associated with the
CAA severity in the AD group. Our results suggest that CAA shares
risk factors with AD and that multiple genetic factors would
be associated with the risk of CAA in the elderly.