Year: 2026
Type: article
Abstract: Collapsing glomerulopathy (CG) in the native kidney is typically associated with heavy proteinuria, rapid progression to kidney failure, and frequent presence of APOL1 kidney risk variants (KRVs).1 In the kidney allograft, CG is rare, often occurring de novo, and has a poor prognosis.2,3 A recent report suggested an association between CG in the kidney allograft and dose-dependent APOL1 KRVs in the donor.4
Source: Kidney International Reports
Language: English
Subfield: Nephrology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,800
OpenAlex ID: W7214793372
