Apolipoprotein E (ApoE) genotype was determined by polymerase chain re
action amplification and restriction digestion of DNA extracted from b
rain tissues of 26 patients with clinically diagnosed and pathological
ly verified lobar atrophy (LA) and from blood of a further 22 patients
with clinical LA. Brain tissue from 50 patients with pathologically c
onfirmed Alzheimer's disease (AD) was also examined, As has been previ
ously reported, the ApoE E4 allele frequency was significantly increas
ed in AD. However, no change in the frequency of ApoE alleles was foun
d in two of the clinical and pathological forms of LA (dementia of fro
ntal type and dementia of frontal type with motor neurone disease) alt
hough the ApoE E4 allele frequency was elevated in cases of non-fluent
progressive aphasia in accordance with the presence of coincidental A
lzheimer-type pathological changes.