Literature DB >> 20113183

Effects of nadir CD4 count and duration of human immunodeficiency virus infection on brain volumes in the highly active antiretroviral therapy era.

Ronald A Cohen1, Jaroslaw Harezlak, Giovanni Schifitto, George Hana, Uraina Clark, Assawin Gongvatana, Robert Paul, Michael Taylor, Paul Thompson, Jeffery Alger, Mark Brown, Jianhui Zhong, Thomas Campbell, Elyse Singer, Eric Daar, Deborah McMahon, Yuen Tso, Constantin T Yiannoutsos, Bradford Navia.   

Abstract

Cerebral atrophy is a well-described, but poorly understood complication of human immunodeficiency virus (HIV) infection. Despite reduced prevalence of HIV-associated dementia in the highly active antiretroviral therapy (HAART) era, HIV continues to affect the brains of patients with chronic infection. In this study we examine patterns of brain volume loss in HIV-infected patients on HAART, and demographic and clinical factors contributing to brain volume loss. We hypothesized that nadir CD4+ lymphocyte count, duration of HIV infection, and age would be associated with reduced cortical volumes. Volumes of cortical and subcortical regions in 69 HIV-infected neuroasymptomatic (NA) individuals and 13 with at least mild acquired immunodeficiency syndrome (AIDS) dementia complex (ADC) were measured using voxel-based morphometry. Demographic and clinical factors (age, plasma HIV RNA level, current and nadir CD4 counts, duration of infection, central nervous system [CNS] penetration of antiretroviral regimen) along with their interactions were entered into a regression model selection algorithm to determine the final models that best described regional brain volumes. Relative to NA, individuals with ADC exhibited decreased total gray matter and parietal cortex volumes and increased total ventricular volumes. Final regression models showed overall cerebral volume, including gray and white matter volume and volumes of the parietal, temporal, and frontal lobes and the hippocampus, were most strongly associated with disease history factors (nadir CD4 and duration of infection). In contrast, basal ganglia volumes were related most strongly to current disease factors, most notably plasma HIV RNA. These findings indicate that individuals with a history of chronic HIV infection with previous episodes of severely impaired immune function, as reflected by reduced nadir CD4+ lymphocyte count, may be at greatest risk for cerebral atrophy. The pattern of HIV-associated brain loss may be changing from a subcortical to a cortical disease among patients who are largely asymptomatic on HAART.

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Year:  2010        PMID: 20113183      PMCID: PMC2995252          DOI: 10.3109/13550280903552420

Source DB:  PubMed          Journal:  J Neurovirol        ISSN: 1355-0284            Impact factor:   2.643


  25 in total

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Review 2.  Antiretroviral therapy in adults: updated recommendations of the International AIDS Society-USA Panel.

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Review 3.  Relationships between cognition and structural neuroimaging findings in adults with human immunodeficiency virus type-1.

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4.  Highly active antiretroviral therapy for patients with AIDS dementia complex: effect on MR imaging findings and clinical course.

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Journal:  J Neurovirol       Date:  2002-04       Impact factor: 2.643

Review 7.  Evidence for a change in AIDS dementia complex in the era of highly active antiretroviral therapy and the possibility of new forms of AIDS dementia complex.

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Review 10.  Neurodegeneration and ageing in the HAART era.

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  119 in total

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Review 4.  Brain dysfunction in the era of combination antiretroviral therapy: implications for the treatment of the aging population of HIV-infected individuals.

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7.  Substance Abuse, Hepatitis C, and Aging in HIV: Common Cofactors that Contribute to Neurobehavioral Disturbances.

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8.  Correlating brain volume and callosal thickness with clinical and laboratory indicators of disease severity in children with HIV-related brain disease.

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9.  The Impact of Alcohol Use on Frontal White Matter in HIV.

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10.  Disrupted brain networks in the aging HIV+ population.

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