R. Cacabelos et al., APOE-RELATED FREQUENCY OF COGNITIVE AND NONCOGNITIVE SYMPTOMS IN DEMENTIA, Methods and findings in experimental and clinical pharmacology, 18(10), 1996, pp. 693-706
Although memory disorders and the aphaso-apraxo-agnosic syndrome are t
he most relevant clinical symptoms in dementia, behavioral changes, mo
od-related disturbances and sleep disorders are the major cause of ins
titutionalization and caregiver concern. In the present study we have
investigated the frequency and progression of cognitive and noncogniti
ve symptoms in Alzheimer's disease (AD) as well as the APOE-related fr
equency of clinical symptoms in dementia. Memory decline (100%), aphas
ia (94%), apraxia (99%), agnosia (94%) and motor dysfunction (90%) app
eared in practically all cases with mild (GDS-3), moderate (GDS 3-4) a
nd seven (GDS 6-7) dementia. The most frequent noncognitive symptoms i
nclude anxiety (76%), depression (68%), behavioral changes (67%), psyc
hotic symptoms (43%), sleep disorders (43%), incontinence (23%) and ce
rebrovascular symptoms (75%). Anxiety, depression, behavioral changes,
psychotic symptoms, motor dysfunction and cognitive deterioration par
alleled the severity of dementia, increasing their frequency from mild
to severe dementia. The most important sleep disorders were irregular
sleep-wake pattern (67%) and insomnia (47%). Disorientation (90%) and
drug administration (88%) appeared to be the most important factors i
n causing sleep disorders in dementia. Disorientation, agitation and m
otor disorders were slightly more frequent in patients with APOE-4/4,
while anxiety and sleep disorders appeared more frequently in APOE-3/4
. Behavioral changes and psychotic symptoms did not show any clear ass
ociation with specific APOE subtypes. In conclusion, our results sugge
st that noncognitive symptoms are very important clinical events in th
e disease progression and in decision making for therapeutic intervent
ion and institutionalization. Furthermore, it is likely that some brai
n dysfunctions leading to particular clinical symptoms might be associ
ated with specific AD genotypes.