A-BETA-PEPTIDE LENGTH AND APOLIPOPROTEIN-E GENOTYPE IN ALZHEIMERS-DISEASE
Citation
M. Gearing et al., A-BETA-PEPTIDE LENGTH AND APOLIPOPROTEIN-E GENOTYPE IN ALZHEIMERS-DISEASE, Annals of neurology, 39(3), 1996, pp. 395-399
Categorie Soggetti
Clinical Neurology",Neurosciences
SICI code
0364-5134(1996)39:3<395:ALAAGI>2.0.ZU;2-B
Abstract
Apolipoprotein E (ApoE) epsilon 4 allele, a risk factor for the develo
pment of Alzheimer's disease (AD), is associated with increased amyloi
d deposition. We examined cerebral cortex in 68 AD cases using antibod
ies to beta-amyloid (A beta) peptides of different length (A beta(1-40
) and A beta(1-42)) and found that the increased plaque frequency obse
rved with epsilon 4 genotypes may be largely attributed to an increase
in A beta(1-40)-positive plaques. Indeed, both the number of A beta(1
-40)-positive plaques, as web as the ratio Of A beta(1-40)/A beta(1-42
)-positive plaques, increased with epsilon 4 dosage. In contrast, the
frequency of A beta(1-42)-immunoreactive plaques was similar for epsil
on 3/epsilon 3, epsilon 3/epsilon 4, and epsilon 4/epsilon 4 genotypes
. ApoE may influence A beta length by facilitating A beta(1-40) deposi
tion onto A beta(1-42)-seeded plaques or by modulating the activity of
a putative carboxypeptidase that forms A beta(1-40) from A beta(1-42)
in situ.