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Resting-state functional magnetic resonance imaging in clade C HIV: within-group association with neurocognitive function
Authors:Lindie du Plessis  Robert H. Paul  Jackie Hoare  Dan J. Stein  Paul A. Taylor  John A. Joska
Affiliation:1.MRC/UCT Medical Imaging Research Unit,University of Cape Town,Cape Town,South Africa;2.Department of Human Biology,University of Cape Town,Cape Town,South Africa;3.Missouri Institute of Mental Health,University of Missouri,Columbia,USA;4.Department of Psychiatry,University of Cape Town,Cape Town,South Africa;5.MRC Unit on Risk & Resilience in Mental Disorders,Cape Town,South Africa;6.African Institute for Mathematical Sciences,Cape Town,South Africa;7.Scientific and Statistical Computing Core,National Institutes of Health,Bethesda,USA;8.HIV Mental Health Research Unit, Division of Neuropsychiatry,University of Cape Town,Cape Town,South Africa
Abstract:Neuroimaging abnormalities are common in chronically infected HIV-positive individuals. The majority of studies have focused on structural or functional brain outcomes in samples infected with clade B HIV. While preliminary work reveals a similar structural imaging phenotype in patients infected with clade C HIV, no study has examined functional connectivity (FC) using resting-state functional magnetic resonance imaging (rs-fMRI) in clade C HIV. In particular, we were interested to explore HIV-only effects on neurocognitive function using associations with rs-fMRI. In the present study, 56 treatment-naïve, clade C HIV-infected participants (age 32.27 ± 5.53 years, education 10.02 ± 1.72 years, 46 female) underwent rs-fMRI and cognitive testing. Individual resting-state networks were correlated with global deficit scores (GDS) in order to explore associations between them within an HIV-positive sample. Results revealed ten regions in six resting-state networks where FC inversely correlated with GDS scores (worse performance). The networks affected included three independent attention networks: the default mode network (DMN), sensorimotor network, and basal ganglia. Connectivity in these regions did not correlate with plasma viral load or CD4 cell count. The design of this study is unique and has not been previously reported in clade B. The abnormalities related to neurocognitive performance reported in this study of clade C may reflect late disease stage and/or unique host/viral dynamics. Longitudinal studies will help to clarify the clinical significance of resting-state alterations in clade C HIV.
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