Topographies of Cortical and Subcortical Volume Loss in HIV and Aging in the cART Era.

J Acquir Immune Defic Syndr

Departments of *Neurology; †Bioengineering; ‡Radiology, Washington University in Saint Louis, St. Louis, MO; and §Hope Center for Neurological Disorders, Washington University in Saint Louis, St. Louis, MO.

Published: December 2016

AI Article Synopsis

  • A study was conducted on brain volume changes in HIV-infected and uninfected participants using a data-driven approach to minimize bias, analyzing the impacts of aging, viral factors, antiretroviral therapy, gender, and smoking.
  • The research involved 51 HIV-uninfected participants and 146 HIV-infected participants, using structural MRI and principal component analysis (PCA) to identify volumetric changes and their associations with cognitive function.
  • Findings revealed significant age-related volumetric changes in cortical regions due to HIV and smoking, with correlations between cortical volume and cognitive scores in HIV+ patients linked to their immune history, while subcortical changes associated with current viral load.

Article Abstract

Objectives: Studies of HIV-associated brain atrophy often focus on a priori brain regions of interest, which can introduce bias. A data-driven, minimally biased approach was used to analyze changes in brain volumetrics associated with HIV and their relationship to aging, viral factors, combination antiretroviral therapy (cART), and gender, and smoking.

Design: A cross-sectional study of 51 HIV-uninfected (HIV-) and 146 HIV-infected (HIV+) participants.

Methods: Structural MRI of participants was analyzed using principal component analysis (PCA) to reduce dimensionality and determine topographies of volumetric changes. Neuropsychological (NP) assessment was examined using global and domain-specific scores. The effects of HIV disease factors (eg, viral load, CD4, etc.) on brain volumes and neuropsychological were investigated using penalized regression (LASSO).

Results: Two components of interest were visualized using principal component analysis. An aging effect predominated for both components. The first component, a cortically weighted topography, accounted for a majority of variance across participants (43.5% of variance) and showed independent effects of HIV and smoking. A secondary, subcortically weighted topography (4.6%) showed HIV-status accentuated age-related volume loss. In HIV+ patients, the cortical topography correlated with global neuropsychological scores and nadir CD4, whereas subcortical volume loss was associated with recent viral load.

Conclusions: Cortical regions showed the most prominent volumetric changes because of aging and HIV. Within HIV+ participants, cortical volumes were associated with immune history, whereas subcortical changes correlated with current immune function. Cognitive function was primarily associated with cortical volume changes. Observed volumetric changes in chronic HIV+ patients may reflect both past infection history and current viral status.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085858PMC
http://dx.doi.org/10.1097/QAI.0000000000001111DOI Listing

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