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HIV in the brain

2001; Lippincott Williams & Wilkins; Volume: 57; Issue: 8 Linguagem: Inglês

10.1212/wnl.57.8.1396

1526-632X

Daniel McClernon, Randall Lanier, S Gartner, P. Feaser, Carlos A. Pardo, Marty St. Clair, Qiming Liao, Justin C. McArthur,

HIV-related health complications and treatments

Objective: To examine the association between HIV RNA levels, patterns of antiretroviral resistance, and neurologic status. Methods: Autopsy samples from 13 HIV-infected subjects were examined for HIV-1 viral RNA (vRNA), and viral reverse transcriptase (RT) genotype was determined. All subjects had been clinically characterized using standard instruments before death. Results: The median HIV-1 vRNA level in brain samples from subjects with moderate dementia was 7.79 log 10 copies/g (range 5.56 to 9.75 log 10 copies/g) compared with 5.44 log 10 copies/g (range 3.51 to 9.32 log 10 copies/g) for mildly demented subjects and 4.87 log 10 copies/g (3.51 to 6.86 log 10 copies/g) for those obtained from nondemented individuals. There were differences between subjects with moderate dementia and nondemented subjects ( p = 0.0002) and between subjects with moderate and mild dementia ( p = 0.0128). No significant differences among the groups were observed for vRNA levels in peripheral tissues. Some demented subjects had relatively low levels of HIV-1 vRNA, and paradoxically some nondemented subjects had high vRNA brain levels. Little subject effect in vRNA was noted in peripheral regions, but high regional variation in vRNA was noted within the brain. Patterns of the major zidovudine (ZDV) RT mutations in brain and peripheral tissues were concordant in most subjects. Subjects with longer duration of exposure to ZDV tended to have lower brain vRNA levels and a greater number of RT mutations than those with limited to no exposure. Conclusions: The presence and severity of HIV dementia correlates with the levels of productive HIV replication within the brain. Other pathophysiologic events (including macrophage activation) probably also contribute to neurologic dysfunction.