Volume 42, Issue 5 pp. 679-688
Original Article
Full Access

Cerebrospinal fluid human immunodeficiency virus type 1 RNA levels are elevated in neurocognitively impaired individuals with acquired immunodeficiency syndrome

Dr. Ronald J. Ellis MD, PhD

Corresponding Author

Dr. Ronald J. Ellis MD, PhD

Department of Neurosciences, University of California, San Diego

University of California, San Diego, HIV Neurobehavioral Research Center, 2760 Fifth Avenue, San Diego, CA 92103Search for more papers by this author
Karen Hsia PhD

Karen Hsia PhD

Department of Pediatrics, University of California, San Diego

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Stephen A. Spector MD

Stephen A. Spector MD

Department of Pediatrics, University of California, San Diego

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Julie A. Nelson BS

Julie A. Nelson BS

Department of Psychiatry, University of California, San Diego

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Robert K. Heaton PhD

Robert K. Heaton PhD

Department of Psychiatry, University of California, San Diego

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Mark R. Wallace MD

Mark R. Wallace MD

San Diego VA Medical Center, San Diego, CA

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Ian Abramson PhD

Ian Abramson PhD

Department of Mathematics, University of California, San Diego

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J. Hampton Atkinson MD

J. Hampton Atkinson MD

Department of Psychiatry, University of California, San Diego

Department of Medicine, Naval Hospital of San Diego

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Igor Grant MD

Igor Grant MD

Department of Psychiatry, University of California, San Diego

Department of Medicine, Naval Hospital of San Diego

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J. Allen McCutchan MD

J. Allen McCutchan MD

Department of Medicine, University of California, San Diego

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First published: 08 October 2004
Citations: 15

Abstract

To determine whether cerebrospinal fluid (CSF) viral burden measurements can assist in the evaluation of human immunodeficiency virus (HIV)-associated neurocognitive disorders, we quantified HIV type 1 (HIV-1) RNA in CSF. Because previous findings suggested that disease stage, lymphocytic pleocytosis, and HIV-1 RNA levels in plasma may influence CSF viral burden, these variables were examined as potential modifying factors. HIV-1 RNA levels were quantified by using a reverse transcriptase–polymerase chain reaction assay. Performance on a comprehensive neuropsychological (NP) battery was noted in 97 prospectively enrolled, HIV-infected subjects. Among subjects with acquired immunodeficiency syndrome (AIDS) (<200 CD4 lymphocytes), NP impairment was associated with significantly higher CSF RNA levels (3.1 vs 1.8 log10 copies/ml; p = 0.02); most impaired subjects met criteria for HIV-associated dementia or minor cognitive–motor disorder. In subjects without AIDS, CSF RNA and NP impairment were unrelated. Before AIDS, CSF RNA was strongly correlated to plasma RNA and to pleocytosis, but in AIDS, CSF and plasma RNA were independent. In conclusion, we found elevated CSF HIV-1 RNA levels in NP impaired subjects with AIDS. Before AIDS, systemic viral replication, possibly through CD4+ mononuclear cell trafficking, may govern virus levels in CSF, whereas in AIDS, CD4 cell depletion may unmask a correlation between increased productive central nervous system HIV infection and clinical neurocognitive disorders.

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