APOLIPOPROTEIN-E (APOE) ALLELE FREQUENCIES IN LATE-ONSET SPORADIC ALZHEIMERS-DISEASE (AD), MIXED DEMENTIA AND VASCULAR DEMENTIA - LACK OF ASSOCIATION OF EPSILON-4 ALLELE WITH AD IN ITALIAN OCTOGENARIAN PATIENTS
R. Scacchi et al., APOLIPOPROTEIN-E (APOE) ALLELE FREQUENCIES IN LATE-ONSET SPORADIC ALZHEIMERS-DISEASE (AD), MIXED DEMENTIA AND VASCULAR DEMENTIA - LACK OF ASSOCIATION OF EPSILON-4 ALLELE WITH AD IN ITALIAN OCTOGENARIAN PATIENTS, Neuroscience letters, 201(3), 1995, pp. 231-234
The Apolipoprotein E (APOE) epsilon 4 allele has been found to be stro
ngly associated with Alzheimer's disease (AD) in most studies conducte
d up to now, though not all investigators have established a similar a
ssociation with other forms of dementia, like vascular dementia. Our s
tudy examined the APOE polymorphism in a sample of 149 dementia patien
ts, of which there were 80 with probable sporadic late-onset AD, 16 wi
th a mixed form of dementia (MD), and 53 with vascular dementia (VD).
An elderly control sample was composed of 126 subjects. The data obtai
ned on the whole AD sample did not confirm the association already rep
orted with APOE epsilon 4. A difference did emerge when the subjects w
ere subdivided on the basis of age at the examination. AD patients age
d less than or equal to 80 years significantly differed from the corre
spondent elderly controls, while no difference was observed between th
e patients aged 81 years or older and controls. This pattern could be
due to a previous disadvantageous effect of the epsilon 4 allele on th
e subjects bearing it. A substantially similar pattern was observed in
the few MD patients, while no differences were found in the two VD su
bgroups. The odds ratio (OR) for AD associated with at least one epsil
on 4 allele was significant and equal to 3.3 (95% CI = 1.2-9.1) for th
e less than or equal to 80 age class, while it was not significant and
equal to 1.1 (95% CI = 0.4-2.8) for the >80 age class. Our data indic
ate that in AD patients aged less than 81 years, epsilon 4 is clearly
associated with AD and that it can be considered a risk factor for AD
chiefly before this age.