Expanding the spectrum of APOL1-related renal disease: de novo collapsing glomerulopathy following kidney transplant
- PMID: 30466562
- PMCID: PMC7274138
- DOI: 10.1016/j.kint.2018.09.006
Expanding the spectrum of APOL1-related renal disease: de novo collapsing glomerulopathy following kidney transplant
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.
Published by Elsevier Inc.
Comment on
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Donor APOL1 high-risk genotypes are associated with increased risk and inferior prognosis of de novo collapsing glomerulopathy in renal allografts.Kidney Int. 2018 Dec;94(6):1189-1198. doi: 10.1016/j.kint.2018.06.024. Epub 2018 Oct 2. Kidney Int. 2018. PMID: 30287079 Free PMC article.
References
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- Santoriello D, et al., Clinical, pathological and APOL1 genotypic analyisis of de novo collapsing glomerulopathy in renal allografts. Kidney Int, 2018. in press.
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- Patel AM, Zenenberg RD, and Goldberg RJ, De novo CMV-associated collapsing focal segmental glomerulosclerosis in a kidney transplant recipient. Transpl Infect Dis, 2018. 20(3): p. e12884. - PubMed
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- Kofman T, et al., APOL1 polymorphisms and development of CKD in an identical twin donor and recipient pair. Am J Kidney Dis, 2014. 63(5): p. 816–9. - PubMed
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