COVID-19-Associated Collapsing Focal Segmental Glomerulosclerosis: A Report of 2 Cases

Yuvraj Sharma1, Samih H Nasr2, Christopher P Larsen3

  • 1Division of Nephrology and Hypertension, Department of Internal Medicine, Henry Ford Health System, Detroit, MI.

Kidney Medicine
|August 11, 2020
PubMed

Insights

Collapsing glomerulopathy, a severe kidney disease, may be a new COVID-19 complication. This risk is higher in African Americans with the apolipoprotein L1 (APOL1) high-risk genotype.

Area of Science:

  • Nephrology
  • Infectious Diseases
  • Genetics

Background:

  • Collapsing glomerulopathy is an aggressive form of focal segmental glomerulosclerosis.
  • The apolipoprotein L1 (APOL1) high-risk genotype is a significant risk factor for collapsing glomerulopathy in African Americans.
  • Coronavirus disease 2019 (COVID-19) is a pandemic with frequent kidney involvement and higher mortality.

Observation:

  • Two African American patients developed acute kidney injury and proteinuria following COVID-19 infection.
  • Kidney biopsies revealed collapsing glomerulopathy, endothelial tubuloreticular inclusions, and acute tubular injury.
  • No direct evidence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral infection in kidney cells was found via electron microscopy or in situ hybridization.

Findings:

  • Both patients possessed the APOL1 high-risk genotype.
  • The clinical presentation and kidney pathology suggest a link between COVID-19 and collapsing glomerulopathy.

Implications:

  • Collapsing glomerulopathy may represent a novel kidney manifestation of COVID-19.
  • This association appears particularly relevant in individuals of African descent carrying the APOL1 high-risk genotype.
  • Further research is needed to elucidate the mechanisms linking COVID-19, APOL1, and collapsing glomerulopathy.

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