HIV infection
often results in MRI-detectable brain atrophy and white matter signal
hyperintensities (WMSHs).
HIV+
patients compared to high-risk controls evidenced global atrophy, reduced
caudate nuclei volume, and a trend to gray matter volume loss but no difference
in white matter volume or in WMSHs. These effects were progressive with CDC
clinical stage such that patients at CDC stage A had values very close to those
of controls, while patients at CDC stage C had the most abnormal values. In
contrast, the relationship between these MRI variables and severity of NP
impairment was much less dramatic, with the mildly to moderately impaired HIV+
subjects showing MRI volume effects greater than or equal to those of the severely
impaired HIV+ subjects. These results suggest that MRI-detectable brain atrophy
secondary to HIV infection is not the primary substrate underlying the
progressive NP impairment in HIV disease.
Neurocognitive disease associated with HIV infection has been
separated into two categories: (1) a more severe form, HIV-1-associated
dementia complex (HADC); and (2) a less severe form, HIV-1-associated minor
cognitive-motor disorder.
MRI-detectable
brain atrophy is strongly associated with CDC stage of systemic HIV disease and
much more weakly associated with severity of NP impairment. When HIV+ subjects
were subgrouped by clinical stage, the MRI differences were directly and
strongly associated with increasing severity of systemic disease.
Opportunistic
infections of the CNS remain the most common specifically identifiable source
of neurologic disability
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