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RESEARCH PAPER ANALYSIS

Kidney transplantation outcomes in children with WT1-associated kidney disease: a single-center cohort study.

In a retrospective single-center cohort of 13 children with WT1-associated kidney disease, all kidney grafts remained functional after a median 32 months, with no disease recurrence, while Epstein–Barr virus viremia and post-transplant lymphoproliferative disorder were notable complications.

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PMID42568457
JournalFrontiers in pediatrics
Publication Date2026-07-24
Ingested2026-08-17 12:23 AM
EXECUTIVE SUMMARY

What the AI sees

In a retrospective single-center cohort of 13 children with WT1-associated kidney disease, all kidney grafts remained functional after a median 32 months, with no disease recurrence, while Epstein–Barr virus viremia and post-transplant lymphoproliferative disorder were notable complications.

WHY IT MATTERS

Research significance

The cohort provides preliminary evidence that kidney transplantation can achieve favorable short- to mid-term graft outcomes in children with WT1-associated disease; it is reasonable but unproven to hypothesize that WT1-informed multidisciplinary tumor, gonadal, and viral surveillance could improve transplant management and reduce serious complications.

ABSTRACT

Source abstract

INTRODUCTION: WT1-associated kidney disease is an important cause of early-onset end-stage kidney disease (ESKD) in children and may be accompanied by Wilms tumor, gonadal tumors, and disorders of sex development (DSD), creating distinctive challenges for kidney transplantation and post-transplant management. METHODS: We retrospectively analyzed 13 children with WT1-associated kidney disease who underwent kidney transplantation at a single center between February 2020 and October 2025. Clinical characteristics, genetic findings, transplant outcomes, and post-transplant complications were reviewed. RESULTS: The median age at disease onset was 2.3 years, the median age at progression to ESKD was 4.1 years, and the median age at transplantation was 5.3 years. Three patients developed Wilms tumor, and three phenotypic females had a 46,XY karyotype with gonadal dysgenesis. Twelve distinct WT1 variants were identified, predominantly exon 9 missense variants and intron 9-10 splice-site variants. After a median follow-up of 32 months, all grafts remained functional, with a median estimated glomerular filtration rate of 68.7 mL/min/1.73 m². Epstein-Barr virus viremia occurred in five patients, and two developed post-transplant lymphoproliferative disorder. No disease recurrence was observed. DISCUSSION: Kidney transplantation achieved favorable short- to mid-term graft outcomes in this cohort. Multidisciplinary surveillance of tumor history, gonadal abnormalities, and post-transplant viral complications remains essential.

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PATIENT-FRIENDLY SUMMARY

Kidney transplantation outcomes in children with WT1-associated kidney disease: a single-center cohort study.

For education only—not personal medical advice.

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