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NEUROLOGY 2004;62:1810-1817
© 2004 American Academy of Neurology

Altered neurometabolite development in HIV-infected children

Correlation with neuropsychological tests

M. A. Keller, MD, T. N. Venkatraman, PhD, A. Thomas, PhD, A. Deveikis, MD, C. LoPresti, PhD, J. Hayes, RN, N. Berman, PhD, I. Walot, MD, S. Padilla, PsyD, J. Johnston-Jones, PhD, T. Ernst, PhD and L. Chang, MD

From the Harbor–UCLA Research and Education Institute (Drs. Keller, Venkatraman, Berman, Walot, Padilla, and Johnston–Jones, J. Hayes), Torrance, University of California, Los Angeles (Drs. Thomas and LoPresti), and Miller’s Children’s Hospital (Dr. Deveikis), Long Beach, CA; and Brookhaven National Laboratory (Drs. Ernst and Chang), Upton, NY.

Address correspondence and reprint requests to Dr. M.A. Keller, Department of Pediatrics, Harbor–UCLA Medical Center, 1000 W. Carson St., Bldg. N25, Box 468, Los Angeles, CA 90509; e-mail: keller{at}rei.edu

Background: HIV-infected children have abnormal cerebral metabolites, measured by proton MR spectroscopy (1H-MRS), but how these abnormalities relate to brain function is unclear.

Methods: Metabolite concentrations in five brain regions of 20 HIV-infected and 13 control children were measured, and these findings were correlated with age, log10 plasma viral load, CD4 count, and neuropsychological scores.

Results: Compared with control subjects, HIV patients had decreased choline concentration [Cho] in left frontal white matter (LFW) (–12%; p = 0.04); those with high viral load (>5,000 HIV RNA copies/mL) had decreased right basal ganglia (RBG) [Cho] (–15%; p = 0.005), and [Cr] (–13%; p = 0.02). Patients with high viral load also had higher [Cho] in the midfrontal gray matter (MFG) (+25%; p = 0.002) and lower myo-inositol [Ins] in the RBG (–18%; p = 0.04) than patients with low HIV viral load. N-Acetyl aspartate concentration ([NAA]) correlated with age in right frontal white matter (RFW) (r = 0.59, p = 0.04), LFW (r = 0.66, p = 0.02), and right hippocampus (RHIP) (r = 0.69, p = 0.02) only in control subjects. In contrast, [Ins] correlated with age in both RFW and LFW (r = 0.71, p = 0.0006; r = 0.65, p = 0.006) only in the HIV patients. Log10 plasma viral load correlated positively with [Ins] in RFW (r = 0.54, p = 0.02) and [Cho] in MFG (r = 0.49, p = 0.04). Compared with control subjects, HIV patients had poorer spatial memory (p = 0.045) and delayed spatial memory correlated with [Cho] in RHIP (r = 0.68, p = 0.02).

Conclusions: These data suggest that normal brain development may be affected in children infected with HIV at birth, particularly evidenced by the lack of age-related increases in the neuronal marker [NAA]. Early, aggressive treatment of infants with HIV before development of encephalopathy is warranted.


Received August 1, 2003. Accepted in final form January 13, 2004.

Additional material related to this article can be found on the Neurology Web site. Go to www.neurology.org and scroll down the Table of Contents for the May 25 issue to find the title link for this article.




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