Expanding the spectrum of APOL1-related renal disease: de novo collapsing glomerulopathy following kidney transplant

Kidney Int. 2018 Dec;94(6):1048-1050. doi: 10.1016/j.kint.2018.09.006.

Abstract

Santoriello et al. report a series of 38 cases of de novo collapsing glomerulopathy following kidney transplant. Associations included acute rejection, viral infection, and APOL1 high-risk genotype (the latter in 9 cases). Risk factors for collapsing glomerulopathy included acute rejection, viral infection, acute vaso-occlusive disease, and an African American donor. The data are suggestive of, but do not directly establish, a role for interferon in these associations.

Publication types

  • Research Support, N.I.H., Intramural
  • Comment

MeSH terms

  • Apolipoprotein L1
  • Genotype
  • Humans
  • Kidney Diseases*
  • Kidney Transplantation*
  • Prognosis

Substances

  • APOL1 protein, human
  • Apolipoprotein L1