Summary
Nephrotic syndrome is a common childhood glomerular disease that is associated with
massive proteinuria and edema. Children with nephrotic syndrome are at risk of chronic
kidney disease, disease-related complications, and treatment-related complications.
Patients with frequently relapsing disease or steroid toxicity may require newer immunosuppressive
medications. However, access to these medications is limited in many African countries
owing to prohibitive cost, the need for frequent therapeutic drug monitoring, and
a lack of appropriate facilities. This narrative review examines the epidemiology
of childhood nephrotic syndrome in Africa, including trends in treatment and patient
outcomes. In most of North Africa, as well as among White and Indian populations in
South Africa, the epidemiology and treatment of childhood nephrotic syndrome closely
resembles that of European and North American populations. Historically, secondary
causes of nephrotic syndrome (eg, quartan malaria nephropathy and hepatitis B–associated
nephropathy) were predominant among Blacks in Africa. Over time, the proportion of
secondary cases has decreased, along with rates of steroid resistance. However, focal
segmental glomerulosclerosis increasingly has been reported among patients with steroid
resistance. There is a need for consensus guidelines for the management of childhood
nephrotic syndrome in Africa. Furthermore, establishing an African nephrotic syndrome
registry could facilitate monitoring of disease and treatment trends, and provide
opportunities for advocacy and research to improve patient outcomes.
Keywords
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Published online: March 10, 2023
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