Neurocognitive impairment in Ugandan children with sickle cell anemia compared to sibling controls: a cross-sectional study.

Journal: Frontiers in stroke

Volume: 3

Issue: 

Year of Publication: 

Affiliated Institutions:  Department of Psychiatry, Makerere University College of Health Sciences, Kampala, Uganda. Department of Neurology, Columbia University Vagelos Medical Center, New York, NY, United States. Department of Mental Health and Community Psychology, Makerere University College of Humanities and Social Sciences, Kampala, Uganda. Global Health Uganda, Kampala, Uganda. Department of Paediatrics and Child Health, Makerere University College of Health Sciences, Kampala, Uganda. Directorate of Paediatrics and Child Health, Mulago National Referral Hospital, Kampala, Uganda. Department of Pediatrics, Columbia University Vagelos Medical Center, New York, NY, United States.

Abstract summary 

The neurocognitive functions in Ugandan children aged 1-12 years with sickle cell anemia (SCA) were compared to their non-SCA siblings to identify risk factors for disease-associated impairment.This cross-sectional study of the neurocognitive functions in children with SCA ( = 242) and non-SCA siblings ( = 127) used age- and linguistically appropriate standardized tests of cognition, executive function, and attention for children ages 1-4 and 5-12. Test scores were converted to locally derived age-normalized -scores. The SCA group underwent a standardized stroke examination for prior stroke and transcranial Doppler ultrasound to determine stroke risk by arterial flow velocity.The SCA group was younger than their siblings (mean ages 5.46 ± 3.0 vs. 7.11 ± 3.51 years, respectively; < 0.001), with a lower hemoglobin concentration (7.32 ± 1.02 vs. 12.06 ± 1.42, < 0.001). The overall cognitive SCA -scores were lower, -0.73 ± 0.98, vs. siblings, -0.25 ± 1.12 ( < 0.001), with comparable findings for executive function of -1.09 ± 0.94 vs. -0.84 ± 1.26 ( = 0.045), respectively. The attention -scores for ages 5-12 for the SCA group and control group were similar: -0.37 ± 1.4 vs. -0.11 ± 0.17 ( = 0.09). The overall differences in SCA status were largely driven by the older age group, as the -scores in the younger subsample did not differ from controls. Analyses revealed the strongest predictors of poor neurocognitive outcomes among the SCA sample to be the disease, age, and prior stroke (each < 0.001). The impacts of anemia and SCA were indistinguishable.Neurocognitive testing in children with SCA compared to non-SCA siblings revealed poorer SCA-associated functioning in children older than age 4. The results indicate the need for trials assessing the impact of disease modification on children with SCA.

Authors & Co-authors:  Bangirana Paul P Boehme Amelia K AK Birabwa Annet A Opoka Robert O RO Munube Deogratias D Mupere Ezekiel E Kasirye Phillip P Muwanguzi Grace G Musiimenta Maxencia M Ru George G Green Nancy S NS Idro Richard R

Study Outcome 

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Statistics
Citations :  Amarachukwu CN, Okoronkwo IL, Nweke MC, and Ukwuoma MK (2022). Economic burden and catastrophic cost among people living with sickle cell disease, attending a tertiary health institution in south-east zone, Nigeria. PLoS ONE 17:e0272491. doi: 10.1371/journal.pone.0272491
Authors :  12
Identifiers
Doi : 1372949
SSN : 2813-3056
Study Population
Male,Female
Mesh Terms
Other Terms
neurocognition;neurocognitive impairment;pediatric sickle cell;sickle cell anemia;sub-Saharan Africa
Study Design
Cross Sectional Study
Study Approach
Country of Study
Uganda
Publication Country
Switzerland