The authors conducted a follow-up study of 16 patients with late-life depre
ssion approximately 6 years after their initial assessment to evaluate the
relationships between apolipoprotein-E (APO-E) status and white-matter hype
rintensities (WMH). Ten patients had WMH at baseline, and four patients dem
onstrated cm increase in WMH size over time. Three of four patients with th
e APO-E epsilon 4 allele demonstrated an increase in WMH over time, and onl
y I of 12 patients Without an epsilon 4 allele had an increase in WMH. Thre
e of four patients with APO-E epsilon 4 allele developed a chronic course o
f major depression at follow-up. Patients with APO-E epsilon 4 had a higher
number of depressive episodes and lower age at onset. APO-E may be a risk
factor for cerebrovascular disease associated with late-life depression and
may affect the clinical characteristics and disease course of depression.