Deep gray matter structures in HIV infection: a proton MR spectroscopic study

AJNR Am J Neuroradiol. 1996 May;17(5):973-8.

Abstract

Purpose: To evaluate the effects of human immunodeficiency virus (HIV) infection on proton metabolites in brain regions carrying the heaviest HIV load.

Methods: We used two-dimensional proton MR spectroscopy with a preselected volume at the level of the third ventricle to measure N-acetyl-aspartate (NAA) and metabolites containing choline (Cho), and creatine (Cr) in the basal ganglia of eight cognitively impaired subjects who were seropositive for HIV and eight control subjects who were seronegative for HIV. Results are expressed as metabolite ratios.

Results: In the thalamus and lenticular nuclei, NAA/Cr was not different between the two groups. NAA/Cho was decreased in both the thalamus and lenticular nuclei of the HIV-positive group compared with the HIV-negative group. Cho/Cr tended to be increased in both the thalamus and lenticular nuclei of the HIV-positive group.

Conclusions: The findings suggest no NAA differences between groups, consistent with negligible neuron loss in the region of the brain that carries the heaviest HIV load. The trends toward increased Cho/Cr are consistent with histopathologic findings of infiltration of subcortical gray matter structures with foamy macrophages, microglia, and lymphocytes, or possibly with gliosis.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • AIDS Dementia Complex / metabolism*
  • AIDS Dementia Complex / pathology
  • Adult
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / metabolism
  • Basal Ganglia / metabolism
  • Brain / metabolism*
  • Brain / pathology
  • Cerebral Ventricles / metabolism
  • Choline / metabolism
  • Corpus Striatum / metabolism
  • Creatine / metabolism
  • Gliosis / pathology
  • HIV Infections / metabolism*
  • HIV Infections / pathology
  • HIV Seronegativity
  • HIV Seropositivity
  • Humans
  • Lymphocytes / pathology
  • Macrophages / pathology
  • Magnetic Resonance Spectroscopy*
  • Male
  • Microglia / pathology
  • Protons
  • Thalamus / metabolism

Substances

  • Protons
  • Aspartic Acid
  • N-acetylaspartate
  • Creatine
  • Choline