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A meta-analysis of the neuropsychological sequelae of HIV infection
This meta-analysis summarizes the broad spectrum of neuropsychological research on HIV disease across a sample of 41 primary studies and an aggregate of 8,616 participants for 10 major neuropsychological ability areas. Analyses of the course of cognitive decline within and across Centers for Disease...
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Published in: | Journal of the International Neuropsychological Society 2002-03, Vol.8 (3), p.410-424 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | This meta-analysis summarizes the broad spectrum of
neuropsychological research on HIV disease across a sample of
41 primary studies and an aggregate of 8,616 participants for
10 major neuropsychological ability areas. Analyses of the course
of cognitive decline within and across Centers for Disease Control
classifications reveals statistically significant cognitive
deficits from asymptomatic HIV to AIDS. Effect sizes (Cohen,
1988) were calculated to reflect between-group (asymptomatic,
symptomatic, AIDS) differences in each neuropsychological domain.
Relatively small effect sizes were obtained for the asymptomatic
(0.05–0.21) patients, and generally small to moderate
effect sizes were obtained for symptomatic (0.18–0.65)
HIV+ patients, with motor functioning exhibiting the greatest
effects in this later disease stage. The most notable deficits
in cognitive functioning were found in the AIDS group with moderate
(attention and concentration) to large (motor functioning) effect
sizes with values ranging from 0.42–0.82. Comparison of
cognitive functioning as a function of disease progression revealed
that motor functioning, executive skills, and information
processing speed were among the cognitive domains showing the
greatest decline from early to later stages of HIV. These findings
indicate that cognitive deficits in the early stages of HIV
are small and increase in the later phases of the illness, and
that specific patterns of cognitive deficits can be detected
with disease progression. These results and their clinical utility
are further discussed. (JINS, 2002, 8,
410–424.) |
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ISSN: | 1355-6177 1469-7661 |
DOI: | 10.1017/S1355617702813212 |