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Published on: October 12, 2018
Default Mode Connectivity in Youth With Perinatally Acquired HIV
Megan M Herting1, Kristina A Uban, Paige L Williams
1From the Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA (MMH, KAU, PG, ERS); Department of Biostatistics, Harvard School of Public Health, Boston, MA (PLW, YH); Feinberg School of Medicine, Northwestern University, Chicago, IL (KM, RY, JC, LW); Department of Neurosciences, Division of Pediatric Neurology, University of California San Diego, La Jolla, CA (SN); Tulane University School of Medicine, New Orleans, LA (RVD); and Keck School of Medicine, University of Southern California, Los Angeles, CA, USA (ERS).
Insights
HIV disease severity impacts brain connectivity in youth. Higher viral load and lower CD4 counts correlate with altered default mode network (DMN) function, potentially explaining cognitive issues in perinatally HIV-infected (PHIV+) youth.
Area of Science:
- Neuroscience
- Immunology
- Pediatrics
Background:
- Youth with perinatally acquired human immunodeficiency virus (PHIV+) have improved survival due to combination antiretroviral therapy.
- Despite treatment advances, PHIV+ youth remain susceptible to cognitive impairments.
Purpose of the Study:
- To investigate the relationship between HIV disease severity markers and default mode network (DMN) functional connectivity in PHIV+ youth.
- To determine if DMN connectivity alterations are associated with cognitive outcomes in this population.
Main Methods:
- Resting-state functional neuroimaging and cognitive testing were performed on 40 PHIV+ youth.
- HIV disease severity was assessed using nadir CD4 counts and peak HIV RNA levels.
- Associations between disease markers, cognitive function, and DMN connectivity were analyzed using multiple regression.
Main Results:
- Global alterations in DMN within- and between-network connectivity were observed in PHIV+ youth.
- Significant associations were found between HIV disease severity markers and DMN connectivity.
- Connectivity patterns involving the posterior cingulate cortex (PCC) and medial prefrontal cortex (mPFC) predicted processing speed, varying with peak HIV RNA.
Conclusions:
- Alterations in DMN connectivity may reflect global brain reorganization in PHIV+ youth.
- These connectivity changes could be compensatory mechanisms related to cognitive processing difficulties.
- HIV disease severity is a significant factor influencing brain network function and cognitive outcomes in PHIV+ youth.
Abstract:
Youth with perinatally acquired human immunodeficiency virus (PHIV+) survive longer with combination antiretroviral therapy, but remain at risk for poor cognitive outcomes. We evaluated whether markers of HIV disease severity relate to default mode resting-state functional connectivity in PHIV+ youth. We conducted resting-state functional neuroimaging and cognitive testing in a subset of 40 PHIV+ youth recruited from a single study site of the Adolescent Master Protocol study conducted by the Pediatric HIV/AIDS Cohort Study (PHACS) network. Current and past HIV disease severity measures (nadir CD4 lymphocyte percentages and peak HIV RNA plasma levels) were obtained from medical charts. We evaluated associations of both HIV disease severity measures and cognitive functioning with between- and within- default mode network (DMN) connectivity using Analysis of Functional NeuroImaging multiple regression analyses, controlling for multiple comparisons. Of the 40 youth, 31 (mean age = 16.5 years) with minimal motion during scans were included. We observed global alterations in DMN within- and between-network connectivity, with significant associations between disease severity and DMN BOLD correlations. Furthermore, patterns of connectivity with the posterior cingulate cortex (PCC) and medial prefrontal cortex (mPFC) that varied as a function of peak HIV RNA were found to predict processing speed ability. Alterations in within- and between-network DMN connectivity in PHIV+ youth may reflect global reorganization of the DMN; this could lead to compensatory alterations in both the within- and between-connectivity of large-scale networks, which may ultimately relate to known cognitive processing difficulties in PHIV+ youth.
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