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).

Medicine
|September 17, 2015
PubMed

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.

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