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Updated: Feb 24, 2026

A Rat Model of EcoHIV Brain Infection
Published on: January 21, 2021
周産期HIV曝露を有する青年における灰白質非対称性の変化:構造的神経画像からの証拠
Jinfeng Lv1, Ling Feng2, Lei Gao1
1Department of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, WH, China.
Objective:
Perinatal exposure to human immunodeficiency virus (HIV) may disrupt typical neurodevelopment, even without infection. Hemispheric lateralization is a key hallmark of this progress, but it remains poorly characterized in this context. This study investigated gray matter (GM) asymmetry in perinatally HIV-exposed adolescents, both infected and uninfected.
Design:
Observational cross-sectional study comparing GM volume and asymmetry across three matched adolescent groups.
Methods:
Adolescents aged 11-17 years were recruited: adolescents living with HIV (ALHIV, n = 35), HIV-exposed uninfected (HEU, n = 70), and typically developing controls (TD, n = 30). All participants underwent high-resolution 3D T1-weighted MRI. GM volume and asymmetry index (AI) were quantified using voxel-wise analyses, with validation based on homotopic parcellation. Group differences were tested using one-way ANOVA with correction for multiple comparisons.
Results:
Significant group effects in GM volume were observed across sensorimotor, visual, frontal, limbic, and cerebellar regions. Both ALHIV and HEU differed from TD across widespread regions, whereas differences between ALHIV and HEU were more spatially restricted (precentral gyrus, calcarine sulcus and superior frontal gyrus). For GM asymmetry, ANOVA revealed differences in the amygdala, insula, orbitofrontal cortex, and thalamus. Both ALHIV and HEU showed notable differences from TD, while differences between ALHIV and HEU were confined to specific thalamic subregions. Regions of interest (ROI)-wise and meta-analytic validation supported these voxel-wise findings.
Conclusions:
Perinatal HIV exposure is associated with atypical GM asymmetry and structural organization in adolescence. Both ALHIV and HEU exhibit deviations from TD peers, with infection status contributing additional localized alterations.

