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.
Via: http://ht.ly/SJ5iV Full article
at: http://goo.gl/pg1ugX
By: Herting MM1, Uban KA, Williams PL, Gautam P, Huo Y, Malee K, Yogev R, Csernansky J, Wang L, Nichols S, Van Dyke R, Sowell ER.
- 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).
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