VISUOSPATIAL ATTENTION IN DEMENTIA OF THE ALZHEIMER TYPE
Cerebral Cortex
Male
CEREBRAL METABOLIC ASYMMETRIES; NUCLEUS RAPHE DORSALIS; MILD SENILE DEMENTIA; VISUAL-ATTENTION; SPATIAL ATTENTION; CLINICAL-DIAGNOSIS; DIVIDED ATTENTION; SELECTIVE ATTENTION; COGNITIVE DEFICITS; DIRECTED ATTENTION
Spatial Behavior
3. Good health
03 medical and health sciences
Cognition
0302 clinical medicine
Alzheimer Disease
Memory
Parietal Lobe
Reaction Time
Visual Perception
Humans
Attention
Dementia
Female
Cues
Psychomotor Performance
Aged
DOI:
10.1093/brain/115.3.711
Publication Date:
2007-01-04T04:52:09Z
AUTHORS (4)
ABSTRACT
Cue-directed shifts of spatial attention were examined for a letter-discrimination task in 15 patients with mild to moderate dementia of the Alzheimer type (DAT) and 15 healthy, age-matched controls. Spatial cues were valid, invalid or neutral in indicating probable target location and were presented either centrally at fixation or peripherally 6.7 degrees to the left or right of fixation. Stimulus-onset asynchrony (SOA) between cue and target was varied between 200 ms and 2000 ms. Reaction time (RT) benefits conferred by valid cues did not differ between the DAT group and the controls. However, RT costs incurred by invalid cues were significantly greater in the DAT group than in the control group. Group differences in RT costs plus benefits occurred at short SOAs (less than 500 ms) for peripheral cues and at long SOAs (greater than 500 ms) for central cues. Reaction time costs plus benefits were correlated with right-left asymmetry in resting levels of cerebral glucose metabolism in the superior parietal lobe for DAT patients but not for controls. The results indicate that focusing of attention to spatial location is intact in early DAT, whereas the disengagement of visuospatial attention is impaired. Automatic attention shifts elicited by peripheral cues reveal abnormalities earlier than attention shifts initiated 'effortfully' by central cues. Intact focusing and impaired disengagement of visuospatial attention may be linked to dysfunction in early DAT of cortico-cortical networks linking the posterior parietal and frontal lobes.
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