Genetic Spectrum of Nephrotic Syndrome: Impact of Podocytopathy in Adult Life

Adv Chronic Kidney Dis. 2022 May;29(3):221-224. doi: 10.1053/j.ackd.2022.04.005.

Abstract

A substantial number of patients with focal segmental glomerulosclerosis (FSGS) have a pathogenic genetic mutation in a podocyte protein as the cause of their disease. The mutations can affect a wide range of cell functions including the actin cytoskeleton, cell adhesion and motility, mitochondrial function, and nuclear pore proteins. The likelihood of a genetic cause declines with age, from approximately 30% in children and adolescents to 10% in adulthood, and the specific proteins involved and the pattern of inheritance differ in the 2 age groups. The presence of a genetic cause for FSGS can have important clinical ramifications including the need for a diagnostic kidney biopsy, medical management, and the risk of recurrent disease after kidney transplantation. This review summarizes the spectrum of genetic causes of nephrotic syndrome, primarily FSGS, in adults with a focus on diagnosis, presentation, and management.

Keywords: Adult; Genetic; Nephrotic syndrome; Podocytopathy.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Glomerulosclerosis, Focal Segmental* / genetics
  • Humans
  • Kidney Transplantation* / adverse effects
  • Mutation
  • Nephrotic Syndrome* / complications
  • Nephrotic Syndrome* / genetics
  • Podocytes* / pathology