Clinical and Imaging Study of Human Immunodeficiency Virus-1—Infected Youth Receiving Highly Active Antiretroviral Therapy: Pilot Study Using Magnetic Resonance Spectroscopy

Author:

Gabis Lidia1,Belman Anita2,Wei Huang 3,Milazzo Maria2,Nachman Sharon4

Affiliation:

1. Child Development Center, Safra Children's Hospital, Tel Hashomer, Israel,

2. Department of Neurology, Stony Brook University, Stony, Brook, NY

3. Department of Radiology, Stony Brook University, Stony, Brook, NY

4. Department of Pediatrics, Stony Brook University, tony, Brook, NY

Abstract

The objective of this study was to correlate clinical and neuropsychologic findings with neuroimaging studies to assess the value of magnetic resonance spectroscopy in detection and monitoring of central nervous system disease of children vertically infected with human immunodeficiency virus (HIV)-1 and receiving highly active antiretroviral therapy. Eight children (four boys) with vertically transmitted stable HIV infection had a neurologic examination, neuropsychologic testing, and a neuroimaging study. The structural magnetic resonance imaging (MRI) and metabolic changes (magnetic resonance spectroscopy) were compared with the cognitive, clinical, and laboratory results. Our results for the eight children who completed the magnetic resonance spectroscopic study showed that a high N-acetylaspartate (NAA) to choline ratio correlated significantly with IQ subtests of arithmetic ( r = .74; P < .034) and comprehension ( r = .77; P = .025). Our results suggest that lower NAA and higher choline values represent neuronal dysfunction and inflammation that can be recognized before anatomic changes appear on MRI. In addition, a low NAA to Cho ratio correlated with poor performance. These data suggest that magnetic resonance spectroscopy can be used as a follow-up tool in addition to the structural MRI. Moreover, a change in a child's performance with a concomitant change in NAA and choline, as measured with magnetic resonance spectroscopy, could indicate the need for more aggressive intervention. ( J Child Neurol 2006;21:485—490; DOI 10.2310/7010.2006.00126).

Publisher

SAGE Publications

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

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