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Published on: January 21, 2021
Neurocognitive function in HIV-positive children in a developing country
S Y Walker1, R B Pierre, C D C Christie
1Department of Child and Adolescent Health, University of the West Indies, Mona, Kingston 7, Jamaica.
Insights
HIV encephalopathy affects over 23% of children in this Jamaican cohort, causing significant neurocognitive dysfunction. Early identification and intervention are crucial for improving the quality of life for affected children.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Human Immunodeficiency Virus (HIV) infection can lead to neurological complications in children.
- HIV encephalopathy is a serious condition affecting cognitive and motor functions.
Purpose of the Study:
- To characterize neurological outcomes in HIV-infected children in Jamaica.
- To determine the prevalence of HIV encephalopathy in this cohort.
Main Methods:
- Retrospective review of data for 287 HIV-infected children (2002-2008).
- Nested case-control study comparing 15 encephalopathic children with 15 matched controls (aged 7-10 years).
- Neurocognitive function assessed using clinical evaluations and standardized tests; outcomes compared using Fisher's exact test and Mann-Whitney U-test.
Main Results:
- Prevalence of HIV encephalopathy was 23.3% (67 children).
- Common neurological abnormalities included delayed milestones, hyperreflexia, spasticity, microcephaly, and quadriparesis.
- Encephalopathic children demonstrated significantly worse neurocognitive function across all assessed domains (p<0.05).
Conclusions:
- A high prevalence of HIV encephalopathy was observed in the studied cohort.
- Significant neurocognitive deficits are associated with HIV encephalopathy in children.
- Early detection and intervention are recommended to enhance patient quality of life.
Objectives:
We aimed to characterize neurological outcomes and determine the prevalence of HIV encephalopathy in a cohort of HIV-infected children in Jamaica.
Methods:
Data for 287 HIV-infected children presenting between 2002 and 2008 were reviewed and neurological outcomes characterized. A nested case-control study was conducted between July and September 2009 used 15 randomly selected encephalopathic HIV-infected children aged 7-10 years and 15 matched controls (non-encephalopathic HIV-infected). Their neurocognitive functions were evaluated using clinical assessment and standardized tests for intelligence, short term memory (visuo-spatial and auditory), selective attention, and fine motor and coordination functions. Outcomes were compared using Fisher's exact test and the Mann-Whitney U-test.
Results:
Sixty-seven (23.3%) children were encephalopathic. The median age at diagnosis of HIV encephalopathy was 1.6 years (interquartile range (IQR) 1.1-3.4 years). Predominant abnormalities were delayed milestones (59, 88.1%), hyperreflexia (59, 86.5%), spasticity (50, 74.6%), microcephaly (42, 61.7%), and quadriparesis (21, 31.3%). The median age of tested children was 8.7 years (IQR 7.6-10.8 years) in the encephalopathic group and 9 years (IQR 7.4-10.7 years) in the non-encephalopathic group. Encephalopathic children performed worse in all domains of neurocognitive function (p<0.05).
Conclusions:
A high prevalence of HIV encephalopathy was noted, and significant neurocognitive dysfunction identified in encephalopathic children. Optimized management through the early identification of neurological impairment and implementation of appropriate interventions is recommended to improve quality of life.
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