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Detection of BK polyomavirus after kidney transplantation: a comparison of urine electron microscopy with plasma polymerase chain reaction
Authors:Justin D. Westervelt  Barbara D. Alexander  Sylvia F. Costa  Sara E. Miller  David N. Howell  Stephen R. Smith
Affiliation:1. Division of Nephrology, Department of Medicine, University of Nebraska Medical Center, , Omaha, NE, USA;2. Division of Infectious Disease and International Health, Department of Medicine, Duke University Medical Center, , Durham, NC, USA;3. Duke Clinical Microbiology Laboratory, Duke University Medical Center, , Durham, NC, USA;4. Department of Pathology, Duke University Medical Center, , Durham, NC, USA;5. Division of Nephrology, Department of Medicine, Duke University Medical Center, , Durham, NC, USA
Abstract:
BK polyomavirus (BKV) infection continues to be a significant source of allograft dysfunction in kidney transplant recipients. The optimal screening method to detect BKV remains undetermined. In this retrospective analysis of 347 consecutive kidney transplant recipients, we compare the diagnostic and screening performance of urine electron microscopy (EM) with plasma polymerase chain reaction (PCR) in testing for BKV, using biopsy‐proved polyomavirus‐associated nephropathy (PVAN) as the gold standard. Sixty‐nine of 347 recipients had a positive screening test for BKV infection. Twenty‐nine patients underwent biopsy, and 11 were diagnosed with PVAN. Sensitivity rates of urine EM and plasma PCR were 88% and 100%, respectively. Specificity rates of urine EM and plasma PCR were 91% and 78%. There was no statistical difference in the operating characteristics of the two tests. The majority of both plasma PCR and urine EM tests were positive in the six months prior to a diagnostic biopsy confirming PVAN. In those patients who had evidence of BKV infection but did not have PVAN, the percentage of positive screening tests decreased with aggressive lowering of immunosuppression. We conclude that urine EM and plasma PCR both function well in screening for BKV infection and in the diagnosis of PVAN. There is an opportunity to detect viral replication, lower immunosuppression, and to prevent PVAN in this population.
Keywords:BK polyomavirus  diagnosis  electron microscopy  kidney transplant  polyomavirus nephropathy
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