Impact of Biosocial Factors on the Neuro-Cognitive Functions of School Children with Sickle Cell Anaemia
Keywords:
sickle cell disease, neurocognition, intelligence, academic performanceAbstract
Background: Sickle cell anaemia (SCA) may impair attention, memory, intelligence and academic performance. This study assessed cognitive function (academic performance and intelligent quotients, (IQ) of children with SCA and determined association between biosocial factors and neurocognition.
Materials and Methods: Cognitive function of 120 children with SCA and 104 matched controls was assessed with Ziler's Draw-A-Person test, academic performance questionnaire (APQ) and average annual academic report. Association with disease
severity, sociodemographic, nutritional and clinico-haematological factors was assessed using multivariate analyses.
Results: More controls than subjects obtained high scores in the APQ, p=0.003. The mean annual academic score was also higher in the controls, p=0.028. However, there was no difference in their mean IQ scores, p=0.831. Disease severity scores, duration of school absenteeism, age and class of SCA children had negative correlation with average annual academic scores (p=0.004, 0.009, 0.031 and 0.038 respectively). IQ scores however positively correlated with average annual scores, p=0.007. Sex distribution, social class, nutritional status and haematological data had no influence on academic performance or IQ. Although, school absenteeism (OR=4.1, 95%CI =2.2–8.4, p=0.003) and IQ (OR=2.9, 95%CI =1.3–7.7, p=0.024) independently predicted academic performance, none of the factors predicted IQ.
Conclusion: Children with SCA had poorer academic performance, although their IQs were comparable to controls. Age, school type, class, disease severity and duration of school absenteeism influences cognition of children with SCA.
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