Idiopathic nephrotic syndrome in South African children

Yassir Mahgoub Bakhiet1,2, Abdullahi Mudi1,2,3, Tholang Khumalo1,2

  • 1Division of Paediatric Nephrology, Department of Paediatrics and Child Health, Charlotte Maxeke Johannesburg Academic Hospital, Johannesburg, South Africa.

Insights

Idiopathic nephrotic syndrome (INS) in children shows varied patterns. Focal segmental glomerulosclerosis (FSGS) is more common in black children, while minimal change disease (MCD) is prevalent in steroid-sensitive cases.

Area of Science:

  • Pediatric Nephrology
  • Renal Pathology
  • Immunology

Background:

  • Idiopathic nephrotic syndrome (INS) exhibits diverse histopathological types and treatment responses.
  • These variations are often linked to ethnicity and geographic origin.

Purpose of the Study:

  • To update knowledge on steroid response and renal histopathology in children with INS.
  • To analyze patterns specific to the South African population.

Main Methods:

  • Retrospective review of medical records for children diagnosed with INS.
  • Data collected from Charlotte Maxeke Johannesburg Academic Hospital.

Main Results:

  • 163 children studied; mean age 5.3 years. Black children constituted the majority (68.1%).
  • Focal segmental glomerulosclerosis (FSGS) was more prevalent in the black racial group (37.8%), while minimal change disease (MCD) was higher in the white racial group (64.3%).
  • 57.7% were steroid-sensitive (SSNS), 42.3% steroid-resistant (SRNS). MCD was common in SSNS (60%), FSGS in SRNS (65.2%).

Conclusions:

  • Higher rates of FSGS observed across racial groups and MCD in the black population compared to prior studies.
  • Findings suggest potential ethnic and geographic influences on INS pathology and steroid response.
Abstract

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