Frontiers in Pediatrics (Mar 2022)

Etiology of Kidney Diseases With Proteinuria in the Gambia/West Africa

  • Udo Vester,
  • Augustin Fombah,
  • Maite Hölscher,
  • Danlami Garba,
  • Mary Tapgun,
  • Pamela Collier N‘Jai,
  • Philipp Mendy,
  • Gibril Bass,
  • Abdul K. Muhammad,
  • Suzanne T. Anderson,
  • Abdoulie Sanneh,
  • Charles Onyeama,
  • Udo Helmchen,
  • Khalifa Bojang,
  • Peter F. Hoyer,
  • Tumani Corrah

DOI
https://doi.org/10.3389/fped.2022.854719
Journal volume & issue
Vol. 10

Abstract

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In West Africa, kidney diseases are frequently seen, but diagnostic and therapeutic options are poor due to limited access to specialized facilities. To unravel the etiology and develop clinical guidelines, we collected clinical data and results of kidney biopsies in 121 pediatric and mostly young adult patients with edema and proteinuria in The Gambia. Workup included clinical examination, urine and serum analysis, and kidney biopsy findings. Selected cases were treated with steroids.ResultsThe median age was 14.9 years (range 1.8–52.0) at presentation. The most frequent underlying histologies were post-infectious glomerulonephritis (PIGN) in 38%, focal-segmental glomerulosclerosis (FSGS) in 30%, minimal change nephrotic syndrome (MCNS) in 15%, and membranous glomerulonephritis (MGN) in 10% of cases. Patients with PIGN were significantly younger and had less proteinuria and higher serum albumin levels than the other three. Infected scabies was seen more often in cases with PIGN. Clinical parameters could not distinguish patients with FSGS, MCNS, and MGN. Steroid response was prompt in patients with MCNS (remission in 10/10 cases) compared to FSGS (4/19) and MGN (0/4). In summary, the clinical histopathological correlation allows a better approach to therapy and can be the basis for urgently needed interventional studies in steroid-resistant cases.

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