Volume 4, Issue 12 pp. 2109-2117
Free Access

Polyomavirus Nephropathy in Pediatric Kidney Transplant Recipients

Jodi M. Smith

Jodi M. Smith

Department of Pediatrics, Division of Nephrology

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Ruth A. McDonald

Ruth A. McDonald

Department of Pediatrics, Division of Nephrology

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Laura S. Finn

Laura S. Finn

Department of Pathology

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Patrick J. Healey

Patrick J. Healey

Department of Surgery

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Connie L. Davis

Connie L. Davis

Division of Nephrology

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Ajit P. Limaye

Corresponding Author

Ajit P. Limaye

Departments of Laboratory Medicine & Medicine (Infectious Diseases), University of Washington, Seattle, WA

* Corresponding author: Ajit P. Limaye, [email protected] [email protected]Search for more papers by this author
First published: 04 October 2004
Citations: 130

Abstract

Given the limited information regarding BK virus-associated nephropathy (BKVN) in pediatric kidney transplant recipients, we assessed the incidence, risk factors, clinical and virologic features of BKVN in pediatric renal transplant recipients at a single transplant center by means of a retrospective cohort study. Histologically confirmed BKVN developed in 6 of 173 (3.5%) kidney transplant recipients at a median of 15 months post-transplant (range: 4–47 months). At a median follow-up of 28 months (range: 5–32), all patients had functioning grafts with mean creatinine and GFR of 1.9 mg/dL and 58 mL/min/1.73 m2, respectively. At the time of diagnosis, all cases had viruria (median 6.1 × 106 copies/mL, range: 105 to 3.9 × 108 copies/mL) and viremia (median 21 000 copies/mL, range: 10 000–40 000 copies/mL). Recipient seronegativity for BKV was significantly associated with the development of BKVN (p = 0.01). BKVN is an important cause of late allograft dysfunction and is strongly associated with recipient seronegativity in pediatric kidney transplant recipients. Further studies to confirm this finding and to define the clinical utility of routine pre-transplant BKV serologic testing are warranted.

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