Abstract

In perinatally HIV-infected (PHIV) children, neurodevelopment occurs in the presence of HIV-infection, and even with combination antiretroviral therapy (cART) the brain can be a reservoir for latent HIV. Consequently, patients often demonstrate long-term cognitive deficits and developmental delay, which may be reflected in altered functional brain activity. Our objective was to examine brain function in PHIV on cART by quantifying the amplitude of low frequency fluctuations (ALFF) and regional homogeneity (ReHo). Further, we studied ALFF and ReHo changes with neuropsychological performance and measures of immune health including CD4 count and viral loads in the HIV-infected youths. We found higher ALFF and ReHo in cerebral white matter in the medial orbital lobe for PHIV (N = 11, age mean ± sd = 22.5 ± 2.9 years) compared to controls (N = 16, age = 22.5 ± 3.0 years), with age and gender as co-variates. Bilateral cerebral white matter showed increased spontaneous regional activity in PHIV compared to healthy controls. No brain regions showed lower ALFF or ReHo in PHIV compared to controls. Higher log10 viral load was associated with higher ALFF and ReHo in PHIV in bilateral cerebral white matter and right cerebral white matter respectively after masking the outcomes intrinsic to the brain regions that showed significantly higher ALFF and ReHo in the PHIV compared to the control. Reductions in social cognition and abstract thinking in PHIV were correlated with higher ALFF at the left cerebral white matter in the left medial orbital gyrus and higher ReHo at the right cerebral white matter in the PHIV patients. Although neuroinflammation and associated neuro repair were not directly measured, the findings support their potential role in PHIV impacting neurodevelopment and cognition.

Details

Title
White matter of perinatally HIV infected older youths shows low frequency fluctuations that may reflect glial cycling
Author
Sarma, Manoj K 1 ; Pal Amrita 2 ; Keller, Margaret A 3 ; Welikson Tamara 4 ; Ventura, Joseph 4 ; Michalik, David E 5 ; Nielsen-Saines, Karin 6 ; Deville, Jaime 6 ; Kovacs, Andrea 7 ; Operskalski Eva 7 ; Church, Joseph A 8 ; Macey, Paul M 2 ; Biswal Bharat 9 ; Albert, Thomas M 1 

 David Geffen School of Medicine at UCLA, Department of Radiological Sciences, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0000 9632 6718) 
 University of California, Los Angeles, UCLA School of Nursing, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0000 9632 6718) 
 Harbor-UCLA Medical Center, Pediatrics, Torrance, USA (GRID:grid.239844.0) (ISNI:0000 0001 0157 6501); The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, USA (GRID:grid.239844.0) (ISNI:0000 0001 0157 6501) 
 David Geffen School of Medicine at UCLA, Psychiatry and Biobehavioral Sciences, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0000 9632 6718) 
 Miller Children’s Hospital of Long Beach, Infectious Diseases-Pediatrics, Long Beach, USA (GRID:grid.415317.5) (ISNI:0000 0004 0444 3773) 
 David Geffen School of Medicine at UCLA, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0000 9632 6718) 
 Keck School of Medicine of University of Southern California, Los Angeles, USA (GRID:grid.42505.36) (ISNI:0000 0001 2156 6853); Los Angeles+USC Medical Center, Los Angeles, USA (GRID:grid.42505.36) (ISNI:0000 0001 2156 6853) 
 Keck School of Medicine of University of Southern California, Children’s Hospital Los Angeles, Pediatrics, Los Angeles, USA (GRID:grid.42505.36) 
 New Jersey Institute of Technology, Biomedical Engineering, Newark, USA (GRID:grid.260896.3) (ISNI:0000 0001 2166 4955) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2486309359
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.