Background: The prevalence of sickle cell trait is extremely high in sub-Saharan Africa. Recent studies have reported the impact of sickle cell carriers on renal function. However, data on renal abnormalities in children with sickle cell trait in this part of the world are unknown. In this report, we assess the glomerular function of children with sickle cell trait (SCT). Methods: A case control study was conducted to assess the glomerular function in 43 Congolese children with sickle cell trait (Hb-AS) matched for age to 65 children with sickle cell anemia in steady state (Hb-SS) and 67 normal controls (Hb-AA). Results: There was a significant difference in the blood pressure levels between the Hb-AS group vs Hb-SS group (P
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Aloni, M. N., Ngiyulu, R. M., Nsibu, C. N., Ekulu, P. M., Makulo, J. R., Gini-Ehungu, J. L., … Lepira, F. B. (2017). Congolese children with sickle cell trait may exhibit glomerular hyperfiltration: A case control study. Journal of Clinical Laboratory Analysis, 31(6). https://doi.org/10.1002/jcla.22143
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