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1.
J Neurovirol ; 18(5): 388-99, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22811264

ABSTRACT

Combination antiretroviral therapy (CART) has proven to effectively suppress systemic HIV burden, however, poor penetration into the central nervous system (CNS) provides incomplete protection. Although the severity of HIV-associated neurocognitive disorders (HAND) has been reduced, neurological disease is expected to exert an increasing burden as HIV-infected patients live longer. Strategies to enhance penetration of antiretroviral compounds into the CNS could help to control HIV replication in this reservoir but also carries an increased risk of neurotoxicity. Efforts to target antiretroviral compounds to the CNS will have to balance these risks against the potential gain. Unfortunately, little information is available on the actions of antiretroviral compounds in the CNS, particularly at concentrations that provide effective virus suppression. The current studies evaluated the direct effects of 15 antiretroviral compounds on neurons to begin to provide basic neurotoxicity data that will serve as a foundation for the development of dosing and drug selection guidelines. Using sensitive indices of neural damage, we found a wide range of toxicities, with median toxic concentrations ranging from 2 to 10,000 ng/ml. Some toxic concentrations overlapped concentrations currently seen in the CSF but the level of toxicity was generally modest at clinically relevant concentrations. Highest neurotoxicities were associated with abacavir, efavarenz, etravirine, nevaripine, and atazanavir, while the lowest were with darunavir, emtracitabine, tenofovir, and maraviroc. No additive effects were seen with combinations used clinically. These data provide initial evidence useful for the development of treatment strategies that might reduce the risk of antiretroviral neurotoxicity.


Subject(s)
Anti-HIV Agents/toxicity , Neurons/drug effects , Animals , Biomarkers/metabolism , Dimethyl Sulfoxide/pharmacology , Drug Interactions , Fetus/cytology , Humans , Membrane Potential, Mitochondrial/drug effects , Microtubule-Associated Proteins/biosynthesis , Mitochondria/drug effects , Mitochondria/metabolism , Neurons/cytology , Neurons/metabolism , Primary Cell Culture , Rats , Rats, Long-Evans
2.
J Neurovirol ; 16(3): 189-202, 2010 May.
Article in English | MEDLINE | ID: mdl-20500018

ABSTRACT

In July 2009, the Center for Mental Health Research on AIDS at the National Institute of Mental Health organized and supported the meeting "NeuroAIDS in Africa." This meeting was held in Cape Town, South Africa, and was affiliated with the 5th IAS Conference on HIV Pathogenesis, Treatment and Prevention. Presentations began with an overview of the epidemiology of HIV in sub-Saharan Africa, the molecular epidemiology of HIV, HIV-associated neurocognitive disorders (HANDs), and HAND treatment. These introductory talks were followed by presentations on HAND research and clinical care in Botswana, Cameroon, Ethiopia, The Gambia, Kenya, Malawi, Nigeria, Senegal, South Africa, Uganda, and Zambia. Topics discussed included best practices for assessing neurocognitive disorders, patterns of central nervous system (CNS) involvement in the region, subtype-associated risk for HAND, pediatric HIV assessments and neurodevelopment, HIV-associated CNS opportunistic infections and immune reconstitution syndrome, the evolving changes in treatment implementation, and various opportunities and strategies for NeuroAIDS research and capacity building in the region.


Subject(s)
AIDS Dementia Complex/epidemiology , Cognition Disorders/epidemiology , Cognition Disorders/virology , Africa/epidemiology , Humans , Neuropsychological Tests , Prevalence
3.
Neuropsychol Rev ; 19(2): 232-49, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19455425

ABSTRACT

Resource-limited regions of the world represent the areas most affected by the global HIV epidemic. Currently, there are insufficient data on the neurocognitive effects of HIV in these areas and neuropsychological studies that have been carried out thus far are marked by inconsistent methods, test batteries, and rating systems for levels of cognitive impairment. These differences in methods, along with genetic variability of both virus and host, differences in co-infections and other co-morbidities, differences in language and culture, and infrastructural deficiencies in many international settings create challenges to the assessment of neurocognitive functioning and interpretation of neuropsychological data. Identifying neurocognitive impairment directly attributable to HIV, exploring relationships between HIV-associated neurocognitive impairment, disease variables, and everyday functioning, evaluating differences in HIV-1 subtype associated neuropathology, and determining implications for treatment remain complicated and challenging goals. Endeavors to establish a more standardized approach to neurocognitive assessments across international studies in addition to accumulating appropriate normative data that will allow more accurate rating of neuropsychological test performance will be crucial to future efforts attempting to achieve these goals.


Subject(s)
Acquired Immunodeficiency Syndrome/complications , Central Nervous System Diseases/diagnosis , Cognition Disorders/diagnosis , HIV Infections/complications , Neuropsychology/standards , Acquired Immunodeficiency Syndrome/pathology , Acquired Immunodeficiency Syndrome/psychology , Central Nervous System Diseases/etiology , Central Nervous System Diseases/psychology , Central Nervous System Diseases/virology , Cognition Disorders/etiology , Cognition Disorders/psychology , Cognition Disorders/virology , Cross-Cultural Comparison , Developing Countries , Global Health , HIV Infections/psychology , Humans , International Cooperation , Neuropsychological Tests , Neuropsychology/methods , Reference Values
4.
J Neurovirol ; 14(2): 87-101, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18370346

ABSTRACT

In July of 2006, the National Institute of Mental Health (NIMH) Center for Mental Health Research on AIDS (CMHRA) sponsored the second conference on the Assessment of NeuroAIDS in Africa, which was held in Arusha, Tanzania. The conference mission was to address the regional variations in epidemiology of HIV-related neurological disorders as well as the assessment and diagnosis of these disorders. Participants discussed and presented data regarding the relevance and translation of neuroAIDS assessment measures developed in resource intensive settings and the challenges of neuro-assessment in Africa, including the applicability of current tools, higher prevalence of confounding diseases, and the complexity of diverse cultural settings. The conference presentations summarized here highlight the need for further research on neuroAIDS in Africa and methods for assessing HIV-related neurological disorders.


Subject(s)
AIDS Dementia Complex/epidemiology , HIV Infections/complications , Nervous System Diseases/etiology , Africa/epidemiology , Antiretroviral Therapy, Highly Active , HIV Infections/epidemiology , Humans , Incidence , Neurosciences/education , Neurosciences/trends , Poverty
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