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26 - Neurologic problems

from Part IV - Clinical manifestations of HIV infection in children

Published online by Cambridge University Press:  03 February 2010

Lucy Civitello
Affiliation:
Department of Neurology, Children's National Medical Center, Washington, DC, National Institutes of Health, Bethesda, MD
Steven L. Zeichner
Affiliation:
National Cancer Institute, Bethesda, Maryland
Jennifer S. Read
Affiliation:
National Cancer Institute, Bethesda, Maryland
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Summary

Introduction

Since the first descriptions of pediatric AIDS in the 1980s, neurodevelopmental abnormalities have been a well-known complication of HIV disease in children, causing significant morbidity and mortality [1–3]. Over the last decade, significant progress has been made in the early diagnosis and treatment of the HIV-infected infant and child. As a result, the prevalence and natural history of neurological illnesses in these patients have changed, with improvement in neurologic outcome in many cases.

The central nervous system (CNS) manifestations of HIV disease can be subdivided into two main groups: (1) those indirectly related to the effects of HIV disease on the brain, such as CNS opportunistic infections (OIs), malignancies, and cerebrovascular disease; and (2) those directly attributable to HIV brain infection.

Peripheral nervous system (PNS) abnormalities occur relatively frequently in adult HIV-infected patients and are usually related to antiretroviral therapy, HIV disease, or OIs [4–7]. Although much less common in infants and children, neuropathies and myopathies do occur, with similar etiologies [8, 9].

Secondary CNS disorders

Opportunistic infections of the CNS

Children with HIV disease have fewer problems with CNS OIs compared with adults, probably because OIs represent reactivation of previous, relatively asymptomatic infections. Nevertheless, CNS OIs can present significant problems in children, and their incidence may increase because children with HIV disease are living longer. Generally, OIs are seen in patients with severe immunosuppression (CD4+ lymphocyte counts less than 200 cells/μ), and in older children and adolescents.

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Publisher: Cambridge University Press
Print publication year: 2005

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References

Belman, A. L., Ultmann, M. H., Horoupian, D.. Neurological complications in infants and children with Acquired Immune Deficiency Syndrome. Ann. Neurol. 8 (1985), 560–6CrossRefGoogle Scholar
Epstein, L. G., Sharer, L. R., Joshi, V. V.. Progressive encephalopathy in children with Acquired Immune Deficiency Syndrome. Ann. Neurol. 17 (1985), 488–96CrossRefGoogle ScholarPubMed
Epstein, L. G., Sharer, L. R., Oleske, J. M.. Neurologic manifestations of Human Immunodeficiency Virus infection in children. Pediatrics 78 (1986), 678–87Google ScholarPubMed
Cornblath, D. R. & McArthur, J. C.Predominantly sensory neuropathy in patients with Acquired Immune Deficiency Syndrome and Acquired Immune Deficiency Syndrome-related complex. Neurology 38 (1988), 794–6CrossRefGoogle Scholar
So, Y. T., Holtzman, D. M., Abrams, D. I. & Olney, R. K.Peripheral neuropathy associated with acquired immunodeficiency. Arch. Neurol. 45 (1988), 945–8CrossRefGoogle ScholarPubMed
Miller, R. G.Neuromuscular complications of Human Immunodeficiency Virus. West. J. Med. 160 (1994), 447–54Google ScholarPubMed
Simpson, S. M. & Olney, R. K.Peripheral neuropathies associated with Human Immunodeficiency Virus infection. Neurol. Clin. 10 (1992), 685–711CrossRefGoogle ScholarPubMed
Raphael, S. A., Price, M. L., Lischner, H. W.. Inflammatory demyelinating polyneuropathy in a child with symptomatic Human Immunodeficiency Virus infection. J. Pediatr. 118 (1991), 242–5CrossRefGoogle Scholar
Floeter, M. K., Civitello, L. A., Everett, C. R.. Peripheral neuropathy in children with Human Immunodeficiency Virus infection. Neurology 49 (1997), 207–12CrossRefGoogle Scholar
Kozlowski, P. B., Sher, J. H., Dickson, D. W. et al. Central Nervous System in pediatric Human Immunodeficiency Virus infection: a multicenter study. In P. B. Kozlowski, D. A. Snider, P. M. Vietze & H. M. Wisniewski (eds.), Brain in Pediatric Acquired Immune Deficiency Syndrome. Basel: Karger (1990), pp. 132–46
Kalayjian, R. C., Cohen, M. L., Bonomo, R. A.. Cytomegalovirus ventriculoencephalitis in Acquired Immune Deficiency Syndrome. Medicine 72 (1993), 67–77CrossRefGoogle Scholar
Holland, N. R., Power, C.Matthews, V. P.. Cytomegalovirus encephalitis in Acquired Immune Deficiency Syndrome. Neurology 44 (1994), 507–14CrossRefGoogle Scholar
Fuller, G. N., Guiloff, R. J., Scaravilli, F.. Combined Human Immunodeficiency Virus-Cytomegalovirus encephalitis presenting with brainstem signs. J. Neurol. Neurosurg. Psychol. 52 (1989), 975–9CrossRefGoogle Scholar
Annunziato, P. W. & Gershon, A. A. Herpesvirus infections in children infected with Human Immunodeficiency Virus. In C. M. Wilfert & P. A. Pizzo (eds.), Pediatric Acquired Immune Deficiency Syndrome: The Challenge of Human Immunodeficiency Virus Infection in Infants, Children and Adolescents. Baltimore: Williams and Wilkins (1998), pp. 205–25
Berger, J. R. F., Scott, G., Albrecht, J.. Progressive Multifocal Leukoencephalopathy in Human Immunodeficiency Virus-l infected children. Acquired Immune Deficiency Syndrome 6 (1992), 837–42Google Scholar
Walsh, T. J., Muller, F. M., Groll, A. et al. Fungal infections in children with Human Immunodeficiency Virus. In C. M. Wilfert & P. A. Pizzo (eds.), Pediatric Acquired Immune Deficiency Syndrome: The Challenge of Human Immunodeficiency Virus Infection in Infants, Children and Adolescents. Baltimore: Williams and Wilkins (1998), 183–204
American Academy of Neurology. Evaluation and management of intracranial mass lesions in Acquired Immune Deficiency Syndrome. Neurology 50 (1998), 21–6CrossRef
Simonds, R. J. & Gonzalo, O. Pneumocystis carinii pneumonia and Toxoplasmosis. In C. M. Wilfert & P. A. Pizzo (eds.), Pediatric Acquired Immune Deficiency Syndrome: The Challenge of Human Immunodeficiency Virus Infection in Infants, Childreni and Adolescents. Baltimore: Williams and Wilkins (1998), pp. 251–65
Belman, A. L., Diamond, G., Dickson, D.. Pediatric Acquired Immune Deficiency Syndrome: neurologic syndromes. Am. J. Dis. Child. 142 (1988), 29–35CrossRefGoogle ScholarPubMed
National Institute of Child Health and Human Development Intravenous Immunoglobulin Study Group. Intravenous Immunoglobulin for the prevention of bacterial infections in children with symptomatic Human Immunodeficiency Virus infection. New Engl. J. Med. 325 (1991), 73–80CrossRef
Cohen, B. A. & Berger, J. R. Neurologic opportunistic infections in Acquired Immune Deficiency Syndrome. In H. E. Gendelman, S. A. Lipton, L. Epstein & S. Swindells (eds.), The Neurology of Acquired Immune Deficiency Syndrome. New York: Chapman and Hall (1998), 303–32
Dickson, D. W., Llen, A. J. F, Werdenheim, K. M. et al. Central Nervous System pathology in children with Acquired Immune Deficiency Syndrome and focal neurologic signs: stroke and lymphoma. In P. B. Kozlowski, D. A. Snider, P. M. Vietze & H. M. Wisniewski (eds.), Brain in Pediatric Acquired Immune Deficiency Syndrome. Basel: Karger (1990), 147–57
Epstein, L. G., DiCarlo, F. J., Joshi, V. V.. Primary lymphoma of the central nervous system in children with Acquired Immune Deficiency Syndrome. Pediatrics 82 (1988), 355–63Google Scholar
Park, Y. D., Belman, A. L., Kim, T. S.. Stroke in pediatric Acquired Immune Deficiency Syndrome. Ann. Neurol. 28 (1990), 303–11CrossRefGoogle Scholar
Frank, Y., Lim, W., Kahn, E.. Multiple ischemic infarcts in a child with Acquired Immune Deficiency Syndrome, varicella-zoster infection and cerebral vasculitis. Pediatric Neurol. 5 (1989), 64–7CrossRefGoogle Scholar
Husson, R. N., Saini, R. & Lewis, L. L.Cerebral artery aneurysms in children infected with Human Immunodeficiency Virus. J. Pediatr. 121 (1992), 927–30CrossRefGoogle ScholarPubMed
Mazzoni, P., Chiriboga, C. A., Millar, W. S. & Rogers, A.Intracerebral aneurysms in Human Immunodeficiency Virus infection: case report and literature review. Pediatr. Neurol. 23 (2000), 252–5CrossRefGoogle ScholarPubMed
Kure, K., Park, Y. D., Kim, T. S.. Immunohistochemical localization of an Human Immunodeficiency Virus epitope in cerebral aneurysmal arteriopathy in pediatric Acquired Immune Deficiency Syndrome. Pediatr. Pathol. 9 (1989), 655–67CrossRefGoogle Scholar
Levy, J. A., Shimabukuro, J., Hollander, H.. Isolation of Acquired Immune Deficiency Syndrome-associated retroviruses from Cerebrospinal Fluid and brain of patients with neurological symptoms. Lancet II (1985), 586–8Google Scholar
Epstein, L. G., Goudsmit, J., Paul, D. A.. Expression of Human Immunodeficiency Virus in Cerebrospinal Fluid of children with progressive encephalopathy. Ann. Neurol. 21 (1987), 397–401CrossRefGoogle ScholarPubMed
Koenig, S., Gendelman, H. E., Orenstein, J. M.. Detection of Acquired Immune Deficiency Syndrome viruses in macrophages in brain tissue from Acquired Immune Deficiency Syndrome patients with encephalopathy. Science 233 (1986), 1089–93CrossRefGoogle ScholarPubMed
Shaw, G. M., Harper, M. R., Hahn, B. H.. HTLV-III infection in brains of children and adults with Acquired Immune Deficiency Syndrome encephalopathy. Science 227 (1985), 177–81CrossRefGoogle Scholar
Resnick, L., DiMarzo-Veronese, F., Schupbach, J.. Intrablood-brain-barrier synthesis of HTLV-III-specific ImmunoglobulinG in patients with neurologic symptoms associated with Acquired Immune Deficiency Syndrome or Acquired Immune Deficiency Syndrome-related complex. New Engl. J. Med. 313 (1985), 1498–504CrossRefGoogle Scholar
Civitello, L. A., Brouwers, P. & Pizzo, P. A.Neurologic and neuropsychologic manifestations in 120 children with symptomatic Human Immunodeficiency Virus infection. Ann. Neurol. 34 (1993), 481Google Scholar
Epstein, L. G. & Sharer, L. R. Neurology of Human Immunodeficiency Virus infection in children. In M. L. Rosenblum, R. M. Levy & D. E. Bredesen (eds.), Acquired Immune Deficiency Syndrome and The Nervous System. New York: Raven Press (1998), 79–101
England, J. A., Baker, C. J., Raskino, C.. Clinical and laboratory characteristics of a large cohort of symptomatic Human Immunodeficiency Virus-infected infants and children. Pediatr. Infect. Dis. J. 15 (1996), 1025–36CrossRefGoogle Scholar
Blanche, S., Newell, M., Mayaux, M.. Morbidity and mortality in European children vertically infected by Human Immunodeficiency Virus-l. Acquired Immune Deficiency Syndrome Hum. Retrovirol. 14 (1997), 442–50CrossRefGoogle Scholar
Lobato, M. N., Caldwell, M. B., Ng, P. & Oxtoby, M. J.Encephalopathy in children with perinatally acquired Human Immunodeficiency Virus infection. J. Pediatr. 126 (1995), 710–15CrossRefGoogle ScholarPubMed
The European Collaborative Study. Neurologic signs in young children with Human Immunodeficiency Virus infection. Pediatr. Inf. Dis. J. 9 (1990), 402–6CrossRef
Sacktor, N., Lyles, R. H. & Skolasky, R.. Human Immunodeficiency Virus-associated neurologic disease incidence changes: Multicenter Acquired Immune Deficiency Syndrome Cohort Study, 1990–1998. Neurology 56 (2001), 257–60CrossRefGoogle Scholar
Brouwers, P., Tudor-Williams, G., DiCarli, C.. Relation between stage of disease and neurobehavioral measures in children with symptomatic Human Immunodeficiency Virus disease. Acquired Immune Deficiency Syndrome 9 (1995), 713–20Google Scholar
Vincent, J., Bash, M., Shanks, D. et al. Neurologic symptoms as the initial presentation of Human Immunodeficiency Virus infection in pediatric patients. In Fifth International Conference on Acquired Immune Deficiency Syndrome, June 1989, Montreal [Abstract TBP 176]
Smith, R., Malee, K., Charurat, M.. Timing of perinatal Human Immunodeficiency Virus-1 infection and rate of neurodevelopment. Pediatr. Infect. Dis. J. 19 (2000), 862–71CrossRefGoogle ScholarPubMed
Tardieu, M., Chenadec, J., Persoz, A.. Human Immunodeficiency Virus-l-related encephalopathy in infants compared with children and adults. Neurology 54 (2000), 1089–95CrossRefGoogle ScholarPubMed
Mintz, M.. Clinical features and treatment interventions for Human Immunodeficiency Virus-associated neurologic disease in children. Semin. Neurol. 19 (1999), 165–76CrossRefGoogle ScholarPubMed
Belman, A. L., Taylor, F., Nachman, S. & Milazzo, M.Human Immunodeficiency Virus-1-associated Central Nervous System disease syndromes in infants and children. Neurology 44 (1994), 168–9Google Scholar
Mintz, M., Tardieu, M., Hoyt, L.. Levodopa therapy improves motor function in Human Immunodeficiency Virus-infected children. Neurology 47 (1996), 1583–5CrossRefGoogle Scholar
Wolters, P., Brouwers, P.Moss, H. & Pizzo, P.Differential receptive and expressive language functioning of children with symptomatic Human Immunodeficiency Virus disease and relation to Computed Tomography scan-brain abnormalities. Pediatrics 95 (1995), 112–19Google ScholarPubMed
Whitt, J. K., Hooper, S. R., Tennison, M. B.. Neuropsychologic functioning of Human Immunodeficiency Virus-infected children with hemophilia. J Pediatr. 122 (1993), 52–9CrossRefGoogle ScholarPubMed
Moss, H., Brouwers, P., Wolters, P. L.. The development of a Q-sort behavioral rating procedure for pediatric Human Immunodeficiency Virus patients. J. Pediatr. Psychol. 19 (1994), 27–46CrossRefGoogle Scholar
Nicholas, J.Dazord, A. & Manificat, S.Evaluation of life quality for children infected by Human Immunodeficiency Virus: validation of a method and preliminary results. Pediatr. Acquired Immune Deficiency Syndrome Human Immunodeficiency Virus Infect. 7 (1996), 254–60Google Scholar
Klaas, P., Wolters, P., Civitello, L. et al. Verbal learning and memory in children with Human Immunodeficiency Virus-1. In International Neuropsychological Society Meeting, 14–17 February 2002
Hernandez, M. & Barros, J. A new challenge in children with Human Immunodeficiency Virus: Psychosis. In Seventh Annual Conference of the Association of Nurses in Acquired Immune Deficiency Syndrome Care, Nashville, Tennessee. 10–12 November 1994 (abstract)
DeCarli, C., Civitello, L. A., Brouwers, P. & Pizzo, P. A.The prevalence of computed axial tomographic abnormalities in 100 consecutive children symptomatic with the human immunodeficiency virus. Ann. Neurol. 34 (1993), 198–205CrossRefGoogle Scholar
Civitello, L., Brouwers, P., DeCarli, C. & Pizzo, P.Calcification of the basal ganglia in children with Human Immunodeficiency Virus infection. Ann. Neurol. 36 (1994), 506Google Scholar
Brouwers, P., Tudor-Williams, G., DeCarli, C.. Interrelations among patterns of change in neurocognitive, Computed Tomography brain imaging, and Cluster of Differentiation4 measures associated with antiretroviral therapy in children with symptomatic Human Immunodeficiency Virus infection. Adv. Neuroimmunol. 4 (1994), 223–31CrossRefGoogle Scholar
Brouwers, P., DeCarli, C., Civitello, L.. Correlation between computed tomographic brain scan abnormalities and neuropsychological function in children with symptomatic Human Immunodeficiency Virus disease. Arch. Neurol. 52 (1995), 39–44CrossRefGoogle ScholarPubMed
Brouwers, P., Civitello, L., DeCarli, C.. Cerebrospinal fluid viral load is related to cortical atrophy and not to intracerebral calcifications in children with symptomatic Human Immunodeficiency Virus disease. J. Neurovirol. 6 (2000), 390–7CrossRefGoogle ScholarPubMed
Civitello, L. A., Wolters, P., Serchuck, L.. Long-term effect of protease inhibitors on neuropsychological function and neuroimaging in pediatric Human Immunodeficiency Virus disease. Ann. Neurol. 48 (2000), 513Google Scholar
Tardieu, M., Blanche, W. & Brunelle, F. Cerebral magnetic resonance imaging studies in Human Immunodeficiency Virus-1 infected children born to seropositive mothers. In Neuroscience of Human Immunodeficiency Virus-1 Infection. (Padova, Italy, 1991), p. 60 (abstract)
Brouwers, P., Vlugt, H., Moss, H.. White matter changes on Computed Tomography brain scans are associated with neurobehavioral dysfunction in children with symptomatic Human Immunodeficiency Virus disease. Child. Neuropsychol. 1 (1995), 93–105CrossRefGoogle Scholar
Menon, D. K., Ainsworth, J. G., Cox, I. J.. Proton MR spectroscopy of the brain in Acquired Immune Deficiency Syndrome dementia complex. J. Comput. Assist. Tomogr. 16 (1992), 538–42CrossRefGoogle Scholar
Lauenberger, J., Haussinger, D., Bayer, S.. Human Immunodeficiency Virus-related metabolic abnormalities in the brain: depiction with proton MR spectroscopy with short echo times. Radiology 199 (1996), 805–10CrossRefGoogle Scholar
Lu, D., Pavlakis, S., Frank, Y.. Proton MR spectroscopy of the basal ganglia in healthy children and children with Acquired Immune Deficiency Syndrome. Radiology 199 (1996), 423–8CrossRefGoogle Scholar
Pavlakis, S. G., Lu, D., Frank, Y.. Brain lactate and N-acetylaspartate in pediatric Acquired Immune Deficiency Syndrome encephalopathy. Am. J. Neuroradiol. 19 (1998), 383–5Google Scholar
Sei, S., Stewart, S. K., Farley, M.. Evaluation of Human Immunodeficiency Virus-1 Ribonucleic Acid levels in cerebrospinal fluid and viral resistance to zidovudine in children with Human Immunodeficiency Virus-encephalopathy. J. Infect. Dis. 174 (1996), 1200–6CrossRefGoogle Scholar
McArthur, J. C., McClernon, D. R., Cronin, M. F.. Relationship between Human Immunodeficiency Virus-associated dementia and viral load in Cerebrospinal Fluid and brain. Ann. Neurol. 42 (1997), 689–98CrossRefGoogle ScholarPubMed
McClernon, D. R., Lanier, R., Gartner, S.. Human Immunodeficiency Virus in the brain: Ribonucleic Acid levels and patterns of zidovudine resistance. Neurology 57 (2001), 1396–401CrossRefGoogle ScholarPubMed
DeLuca, A., Ciancio, B. C., Larussa, D.. Correlates of independent Human Immunodeficiency Virus-1 replication in the Central Nervous System and of its controls by antiretrovirals. Neurology 59 (2002), 342–7CrossRefGoogle Scholar
Ellis, R. J., Moore, D. J., Childers, M. E.. Progression to neuropsychologic impairment in Human Immunodeficiency Virus infection predicted by elevated Cerebrospinal Fluid levels of Human Immunodeficiency Virus Ribonucleic Acid. Arch. Neurol. 59 (2002), 923–8CrossRefGoogle Scholar
Mintz, M., Rapaport, T. R., Oleske, J. M.. Elevated levels of tumor necrosis factor are associated with progressive encephalopathy in children with Acquired Immune Deficiency Syndrome. Am. J. Dis. Child. 143 (1989), 771–4Google Scholar
Zakum, D., Orav, J., Korengay, J.. Correlation of ribonucleic acid polymerase chain reaction acid-dissociated p24 antigen, and neopterin with progression of disease: a retrospective, longitudinal study of vertically-acquired Human Immunodeficiency Virus-I infection in children. J. Pediatr. 130 (1997), 898–905Google Scholar
McArthur, J. C., Nance-Sproson, T. E., Griffin, D. E.. The diagnostic utility of elevation in Cerebrospinal Fluid beta-2-microglobulin in Human Immunodeficiency Virus-1 dementia. Neurology 42 (1992), 1707–12CrossRefGoogle ScholarPubMed
Brouwers, P., Heyes, M. P., Moss, H. A.. Quinolinic acid in the Cerebrospinal Fluid of children with symptomatic Human Immunodeficiency Virus type 1 disease: relationship to clinical status and therapeutic response. J. Infect. Dis. 168 (1993), 1380–6CrossRefGoogle Scholar
Cinque, P., Vago, L., Mengozzi, M.. Elevated Cerebrospinal Fluid levels of monocyte chemotactic protein-1 correlate with Human Immunodeficiency Virus-1 encephalitis and local viral replication. Acquired Immune Deficiency Syndrome 12 (1998), 1327–32Google ScholarPubMed
Sharer, L. R. & Mintz, M. Neuropathology of Acquired Immune Deficiency Syndrome in children. In F. Scaravilli (ed.), The Neuropathology of Human Immunodeficiency Virus Infection. Berlin: Springer-Verlag (1993) pp. 201–14
Sharer, L. R. Neuropathologic aspects of Human Immunodeficiency Virus-1 infection in children. In H. E. Gendelman, S. A. Lipton, L. Epstein & S. Swindells (eds.), The Neurology of Acquired Immune Deficiency Syndrome. New York: Chapman and Hall (1998), pp. 408–18
Everall, I. P., Luthert, P. J. & Lantos, P. L.Neuronal loss in the frontal cortex in Human Immunodeficiency Virus infection. Lancet 337 (1991), 119–21CrossRefGoogle Scholar
Davis, L., Hjelle, B. L., Miller, V. E.. Early viral brain invasion in iatrogenic Human Immunodeficiency Virus infection. Neurology 42 (1992), 1736–9CrossRefGoogle ScholarPubMed
Nottett, H. S. & Shawan, S. Human Immunodeficiency Virus-1 entry into brain. Mechanisms for the infiltration of Human Immunodeficiency Virus-1 infected macrophages across the blood-brain-barrier. In H. E. Gendelman, S. A. Lipton, L. Epstein, S. Swindells (eds.), The Neurology of Acquired Immune Deficiency Syndrome. New York: Chapman and Hall (1998), 49–60
Conant, K., Irani, D., Sjulson, L. et al. A potential role for matrix metalloproteinases in the development of Human Immunodeficiency Virus dementia. In 6th Conference on Retroviruses and Opportunistic Infections. Chicago, Interleukin (1999) [Abstract 282]
Ghorpade, A., Che, M., Labenz, C. et al. Mononuclear phagocytes secrete metalloproteinases that affect the neuropathogenesis of Acquired Immune Deficiency Syndrome dementia. In 6th Conference on Retroviruses and Opportunistic Infections. Chicago, Interleukin (1999) [Abstract 283]
Nath, A.Pathobiology of Human Immunodeficiency Virus dementia. Semin. Neurol. 19 (1999), 113–27CrossRefGoogle ScholarPubMed
Zheng, J. & Gendelman, H. E.The Human Immunodeficiency Virus-1 associated dementia complex: a metabolic encephalopathy fueled by viral replication in mononuclear phagocytes. Curr. Opin. Neurol. 10 (1997), 319–25CrossRefGoogle ScholarPubMed
Tornatore, C., Chandra, R., Berger, J. R. & Major, E. O.Human Immunodeficiency Virus-1 infection of subcortical astrocytes in the pediatric central nervous system. Neurology 44 (1994), 481–7CrossRefGoogle ScholarPubMed
Strizki, J. M., Albright, A. V., Sheng, H.. Infection of primary human microglia and monocyte-derived macrophages with acute Human Immunodeficiency Virus-1 isolates: evidence of differential tropism. J. Virol. 70 (1996), 7564–662Google Scholar
Basagra, O., Lavi, E., Bobroski, L.. Cellular reservoirs of Human Immunodeficiency Virus-1 in the Central Nervous System of infected individuals: identification by combination of in situ Polymerase Chain Reaction and immunohistochemistry. Acquired Immune Deficiency Syndrome 10 (1996), 573–85Google Scholar
Brew, B. J., Wesselngh, S. L., Gonzabeg, M.. How Human Immunodeficiency Virus leads to neurological disease. Med. J. Aust. 164 (1996), 233–4Google ScholarPubMed
Nath, A., Haughey, N. J., Jones, M.. Synergistic neurotoxicity by Human Immunodeficiency Virus proteins Tat and gp120: protection by memantine. Ann. Neurol. 47 (2000), 186–943.0.CO;2-3>CrossRefGoogle ScholarPubMed
Magnuson, D. S., Knudson, B. E., Geiger, J. D.. Human Immunodeficiency Virus type 1 Tat activates non-N-methyl-D-aspartate excitatory amino acid receptors and causes neurotoxicity. Ann. Neurol. 37 (1995), 373–83CrossRefGoogle ScholarPubMed
Selmaj, K. W. & Rane, C. S.Tumor necrosis factor mediates myelin and oligodendrocyte damage in vitro. Ann. Neurol. 23 (1988), 339CrossRefGoogle ScholarPubMed
Talley, A. K., Dewhurst, S., Perry, S. W.. Tumor necrosis factor alpha-induced apoptosis in human neuronal cells: protection by the antioxidant N-acetylcysteine and the genes bcl-2 and cmA. Mol. Cell Biol. 15 (1995), 2359–66CrossRefGoogle Scholar
Genis, P., Jett, M., Bernton, E. W.. Cytokines and arachidonic metabolites produced during Human Immunodeficiency Virus-infected macrophage-astroglia interactions: implications for the neuropathogenesis of Human Immunodeficiency Virus disease. J. Exp. Med. 176 (1992), 1703–18CrossRefGoogle Scholar
Bukrinsky, M. I., Nottet, H. S., Schmidtmayerova, H.. Regulation of nitric oxide synthase activity in Human Immunodeficiency Virus-1 infected monocytes: implications for Human Immunodeficiency Virus-associated neurologic disease. J. Exp. Med. 181 (1995), 735–45CrossRefGoogle Scholar
Sanders, V. J., Pittman, C. A., White, M. G.. Chemokines and receptors in Human Immunodeficiency Virus encephalitis. Acquired Immune Deficiency Syndrome 12 (1998), 1021–6Google Scholar
Zheng, J., Thylan, M. R., Ghorpade, A. et al. Linkages between intracellular CXCR4 signaling, neuronal apoptosis, and the neuropathogenic mechanisms for Human Immunodeficiency Virus-1-associated dementia. In 6th Conference on Retroviruses and Opportunistic Infections, Chicago, Interleukin (1999) [Abstract 288]
Samson, M., Libert, F., Doranz, B. J.. Resistance to Human Immunodeficiency Virus-1 infection in caucasian individuals bearing mutant alleles of the CCR5 chemokine receptor gene. Nature 382 (1966), 722–5CrossRefGoogle Scholar
Petito, C. K. & Roberts, B.Evidence of apoptotic cell death in Human Immunodeficiency Virus encephalitis. Am. J. Pathol. 146 (1995), 1121–30Google Scholar
Lipton, S. A.Similarity of neuronal cell injury and death in Acquired Immune Deficiency Syndrome dementia and focal cerebral ischemia: potential treatment with N-Methyl-D-Aspartate open-channel blockers and nitric-oxide-related species. Brain Patho. 6 (1996), 507–17CrossRefGoogle Scholar
Ferrarese, C., Aliprandi, A., Tremolizzo, L.. Increased glutamate in Cerebrospinal Fluid and plasma of patients with Human Immunodeficiency Virus dementia. Neurology 57 (2001), 671–5CrossRefGoogle Scholar
Pialeux, G., Fournier, S., Moulignier, A.. Central Nervous System as a sanctuary for Human Immunodeficiency Virus-1 infection despite treatment with zidovudine, lamivudine and indinavir. Acquired Immune Deficiency Syndrome 11 (1997), 1302–3Google Scholar
Gisslen, M., Norkrans, G. & Svennerholm, B.Human Immunodeficiency Virus-1 Ribonucleic Acid detectable with ultrasensitive Polymerase Chain Reaction in plasma but not in Cerebrospinal Fluid during combination treatment with zidovudine, and indinavir. Acquired Immune Deficiency Syndrome 12 (1998), 114–5Google Scholar
Pomerantz, R. J.Residual Human Immunodeficiency Virus-1 infection during antiretroviral therapy: the challenge of viral persistence. Acquired Immune Deficiency Syndrome 15 (2001), 1201–11Google ScholarPubMed
Stingele, K., Haas, J., Zimmermann, T.. Independent Human Immunodeficiency Virus replication in paired Cerebrospinal Fluid and blood viral isolates during antiretroviral therapy. Neurology 56 (2001), 355–61CrossRefGoogle ScholarPubMed
McArthur, J. C., Sacktor, N. & Selnes, O.Human Immunodeficiency Virus-associated dementia. Semin. Neurol. 19 (1999), 129–50CrossRefGoogle ScholarPubMed
Enting, R. H., Hoetelmans, M. W., Lange, J. M. A. Antiretriviral drugs and the Central Nervous System. Acquired Immune Deficiency Syndrome 12 (1998), 1941–55Google Scholar
Pizzo, P., Eddy, J., Falloon, J.. Effect of continuous IV infusion of zidovudine in children with symptomatic Human Immunodeficiency Virus infection. New Engl. J. Med. 319 (1988), 889–96CrossRefGoogle Scholar
McKinney, R. E., Maha, M. A., Connor, E. M.. A multicenter trial of oral zidovudine in children with advanced human immunodeficiency virus disease. The Protocol 043 Study Group. New Engl. J. Med. 324 (1991), 1018–25CrossRefGoogle ScholarPubMed
Portegies, P., Gans, J., Lange, J. M.. Declining incidence of Acquired Immune Deficiency Syndrome dementia complex after introduction of zidovudine treatment. Br. Med. J. 299 (1989), 819–21CrossRefGoogle ScholarPubMed
Kline, M. W., Dunkle, L. M., Church, J. A.. A phase I/II evaluation of stavudine (Stavudine) in children with Human Immunodeficiency Virus infection. Pediatrics 96 (1995), 247–52Google ScholarPubMed
Butler, K. M., Husson, R. N., Balis, F. M.. Dideoxyinosine in children with symptomatic Human Immunodeficiency Virus infection. New Engl. J. Med. 324 (1991), 137–44CrossRefGoogle ScholarPubMed
Arendt, G., Giesen, H. V., Hefter, H. & Theisen, A, . Therapeutic effects of nucleoside analogues on psychomotor slowing in Human Immunodeficiency Virus infection. Acquired Immune Deficiency Syndrome 15 (2001), 493–500Google Scholar
Englund, J. A., Baker, C. J., Raskino, C.. A trial comparing zidovudine, didanosine, and combination therapy for initial treatment of symptomatic Human Immunodeficiency Virus-infected children. New Engl. J. Med. 336 (1997), 1704–12CrossRefGoogle Scholar
Sacktor, N., Tarwater, P. M., Skolasky, M. A.. Cerebrospinal Fluid antiretroviral drug penetrance and the treatment of Human Immunodeficiency Virus-associated psychomotor slowing. Neurology 57 (2001), 542–4CrossRefGoogle Scholar
Luzuriaga, K., Bryson, Y., Krogstad, P.. Combination treatment with zidovudine, didanosine, and nevirapine in infants with Human Immunodeficiency Virus-1 infection. New Engl. J. Med. 336 (1997), 1343–9CrossRefGoogle Scholar
Martin, C., Sonnerborg, A., Svensson, J. O. & Stahle, L, . Indinavir-based treatment of Human Immunodeficiency Virus-1 infected patients: efficacy in the central nervous system. Acquired Immune Deficiency Syndrome 13 (1999), 1227–32Google ScholarPubMed
Mueller, B. U., Nelson, R. P. Jr., Sleasman, J.. A phase I/II study of the protease inhibitor ritonavir in children with Human Immunodeficiency Virus infection. Pediatrics 101 (1998), 335–43CrossRefGoogle ScholarPubMed
Mueller, B. U., Sleasman, J., Nelson, R. P. Jr.. A phase I/II study of the protease inhibitor indinavir in children with Human Immunodeficiency Virus infection. Pediatrics 102 (1998), 101–9CrossRefGoogle Scholar
Suarez, S., Baril, L., Stankoff, B.. Outcome of patients with Human Immunodeficiency Virus-1-related cognitive impairment on Highly Active Antiretroviral Therapy. Acquired Immune Deficiency Syndrome 15 (2001), 195–200Google Scholar
Maschke, M., Kastrup, O., Esser, S.. Incidence and prevalence of neurological disorders associated with Human Immunodeficiency Virus since the introduction of Highly Active Antiretroviral Therapy. J. Neurol. Neurosurg. Psychiatry 69 (2000), 376–80CrossRefGoogle ScholarPubMed
Chang, L., Ernst, T., Leonido-Yee, M.. Highly Active Antiretroviral Therapy reverses brain metabolite abnormalities in mild Human Immunodeficiency Virus dementia. Neurology 53 (1999), 782–9CrossRefGoogle Scholar
Stankoff, B., Tourbah, A., Suarez, S.. Clinical and spectroscopic improvement in Human Immunodeficiency Virus-associated cognitive impairment. Neurology 56 (2001), 112–15CrossRefGoogle Scholar
Chang, L., Witt, M., Miller, E.. Cerebral metabolite changes during the first nine months of Highly Active Antiretroviral Therapy. Neurology 56: A474 (Suppl. 3) (2001)Google Scholar
Tepper, V. J., Farley, H., Rothman, M. I.. Neurodevelopmental/neuroradiologic recovery of a child infected with Human Immunodeficiency Virus after treatment with combination antiretroviral therapy using the Human Immunodeficiency Virus-specific protease inhibitor, ritonavir. Pediatrics 101: e7 (1998)CrossRefGoogle Scholar
Rosenfeldt, V., Henrik, N., Valerius, H. & Paerregaard, A.Regression of Human Immunodeficiency Virus-associated progressive encephalopathy of childhood during Highly Active Antiretroviral Therapy. Scand J. Infect. Dis. 32 (2000), 571–4Google Scholar
Sandt, I. C. J., Vos, C. M. P., Nabulsi, L.. Assessment of active transport of Human Immunodeficiency Virus protease inhibitors in various cell lines and the in vitro blood-brain barrier. Acquired Immune Deficiency Syndrome 15 (2001), 483–91Google ScholarPubMed
Simpson, D. M.Human Immunodeficiency Virus-associated dementia: review of pathogenesis, prophylaxis and treatment studies of zidovudine therapy. Clin. Infect. Dis. 29 (1999), 19–34CrossRefGoogle ScholarPubMed
Geisen, H. J., Hefter, H., Jablonski, H. & Arendt, G.Highly Active Antiretroviral Therapy is neuroprophylactic in Human Immunodeficiency Virus-1 infection. J. Acquired Immune Deficiency Syndrome 23 (2000), 380–5Google Scholar
Chao, C. C., Hu, S., Close, K.. Cytokine release from microglia: differential inhibition by pentoxifylline and dexamethasone. J. Infect. Dis. 166 (1992), 847–53CrossRefGoogle ScholarPubMed
Steihm, E. R., Bryson, Y. S., Frenhal, L. M.. Prednisone improves Human Immunodeficiency Virus encephalopathy in children. Pediatr. Infect. Dis. J. 11 (1992), 49CrossRefGoogle Scholar
Peterson, P. K., Hu, S., Sheng, W. S.. Thalidomide inhibits Tumor Necrosing Factor-alpha production by lipopolysaccharide and lipoarabine mannah-stimulated human microglial cells. J. Infect. Dis. 172 (1995), 1137–40CrossRefGoogle Scholar
Galgani, S., Balestra, P., Narciso, P.. Nimodipine plus zidovudine versus zidovudine alone in the treatment of Human Immunodeficiency Virus-1-associated cognitive deficits. Acquired Immune Deficiency Syndrome 11 (1997), 1520–1Google Scholar
Navia, B. A., Yiannoutsos, C. T., Chang, L.. Acquired Immune Deficiency Syndrome Clinical Trials Group 301: a phase II randomized double-blind, placebo-controlled trial of memantine for Acquired Immune Deficiency Syndrome dementia complex. Neurology 56 (2001) A474–5 (Suppl. 3)Google Scholar
Turchan, J. T., Gairola, C., Schifitto, G.. Cerebrospinal Fluid from Human Immunodeficiency Virus demented patients causes mitochondrial dysfunction reversible by novel antioxidants. Neurology 56 (2001), 475 (Suppl 3)Google Scholar
Dana Consortium on the therapy of Human Immunodeficiency Virus dementia and related cognitive disorders: a randomized, double-blind, placebo-controlled trial of deprenyl and thioctic acid in Human Immunodeficiency Virus-associated cognitive impairment. Neurology 50 (1998), 645–51CrossRef
Whitaker, R.Neuropsychiatry of Human Immunodeficiency Virus-associated dementia. Psychiatr. Times (March 2001), 57–62Google Scholar
Petito, C. K., Navia, B. A., Cho, E. S.. Vacuolar myelopathy pathologically resembling subacute combined degeneration in patients with Acquired Immune Deficiency Syndrome. New Engl. J. Med. 312 (1985), 874–9CrossRefGoogle Scholar
Dickson, D. W., Belman, A. L., Tin, T. S.. Spinal cord pathology in pediatric Acquired Immune Deficiency Syndrome. Neurology 39 (1989), 227–35CrossRefGoogle Scholar
Dalakas, Mc., Illa, I., Pezeshkpour, G. H.. Mitochondrial myopathy caused by long-term zidovudine therapy. New Engl. J. Med. 322 (1990), 1098–105CrossRefGoogle ScholarPubMed
Walter, E. B., Drucker, R. P., McKinney, R. E.. Myopathy in Human Immunodeficiency Virus-infected children receiving long-term zidovudine therapy. J. Pediatr. 119 (1991), 152–5CrossRefGoogle ScholarPubMed

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  • Neurologic problems
    • By Lucy Civitello, Department of Neurology, Children's National Medical Center, Washington, DC, National Institutes of Health, Bethesda, MD
  • Edited by Steven L. Zeichner, National Cancer Institute, Bethesda, Maryland, Jennifer S. Read, National Cancer Institute, Bethesda, Maryland
  • Book: Textbook of Pediatric HIV Care
  • Online publication: 03 February 2010
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544798.029
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  • Neurologic problems
    • By Lucy Civitello, Department of Neurology, Children's National Medical Center, Washington, DC, National Institutes of Health, Bethesda, MD
  • Edited by Steven L. Zeichner, National Cancer Institute, Bethesda, Maryland, Jennifer S. Read, National Cancer Institute, Bethesda, Maryland
  • Book: Textbook of Pediatric HIV Care
  • Online publication: 03 February 2010
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544798.029
Available formats
×

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To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Neurologic problems
    • By Lucy Civitello, Department of Neurology, Children's National Medical Center, Washington, DC, National Institutes of Health, Bethesda, MD
  • Edited by Steven L. Zeichner, National Cancer Institute, Bethesda, Maryland, Jennifer S. Read, National Cancer Institute, Bethesda, Maryland
  • Book: Textbook of Pediatric HIV Care
  • Online publication: 03 February 2010
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544798.029
Available formats
×