Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)

Background. BK virus (BKV) is the cause of nephropathy. Because BKV nephropathy can progress to graft loss, early diagnosis of BKV infection is very important. In this study, we aimed to investigate the utility of quantifying cells with intranuclear inclusion bodies (decoy cells) in urinary sediment...

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Main Authors: Yoshiteru Yamada, PhD, Tomohiro Tsuchiya, MD, PhD, Isao Inagaki, Mitsuru Seishima, MD, PhD, Takashi Deguchi, MD, PhD
Format: Article
Language:English
Published: Wolters Kluwer 2018-02-01
Series:Transplantation Direct
Online Access:http://journals.lww.com/transplantationdirect/fulltext/10.1097/TXD.0000000000000759
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spelling doaj-c146faeb246c41a0b8801921e4af3bef2020-11-24T23:25:47ZengWolters KluwerTransplantation Direct2373-87312018-02-0142e34010.1097/TXD.0000000000000759201802000-0007Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)Yoshiteru Yamada, PhD0Tomohiro Tsuchiya, MD, PhD1Isao Inagaki2Mitsuru Seishima, MD, PhD3Takashi Deguchi, MD, PhD41 Department of Urology, Gifu University Graduate School of Medicine, Gifu, Japan.1 Department of Urology, Gifu University Graduate School of Medicine, Gifu, Japan.2 Department of Informative Clinical Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.2 Department of Informative Clinical Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.1 Department of Urology, Gifu University Graduate School of Medicine, Gifu, Japan.Background. BK virus (BKV) is the cause of nephropathy. Because BKV nephropathy can progress to graft loss, early diagnosis of BKV infection is very important. In this study, we aimed to investigate the utility of quantifying cells with intranuclear inclusion bodies (decoy cells) in urinary sediment for the screening and monitoring of BKV infection in renal transplant recipients at our hospital. Methods. This was a retrospective single-center study. Urine sediment examination was performed at each outpatient visit, and the number of decoy cells was measured in the whole microscopic field. Patients (n = 41) were divided into the BK viremia group (blood positive for BKV DNA by polymerase chain reaction [PCR]) and non-BK viremia group (blood negative for BKV DNA by PCR), and the decoy cell count in urinary sediments was examined. Results. The maximum decoy cell count was significantly higher (P = 0.04) in the BK viremia group than in the non-BK viremia group. In the receiver operating characteristic curve for the maximum decoy cells, the cutoff value was 507 cells. The area under the receiver operating characteristic curve was 0.8774 (95% confidence interval, 0.7739-0.9810). The number of decoy cells at the time of appearance in the BK viremia group was not significantly different from that in the non-BK viremia group. However, the BK viremia group showed an increasing trend, whereas the non-BK viremia group showed a decreasing trend, in the number of decoy cells. There was a positive correlation between the number of decoy cells and the data from the urine BKV-DNA PCR quantification (correlation coefficient [r] = 0.74). Conclusions. Measurement of decoy cells in urinary sediments may predict early BKV infection, and if performed quickly, it may be useful for screening and continuous monitoring of BKV infection in renal transplant recipients.http://journals.lww.com/transplantationdirect/fulltext/10.1097/TXD.0000000000000759
collection DOAJ
language English
format Article
sources DOAJ
author Yoshiteru Yamada, PhD
Tomohiro Tsuchiya, MD, PhD
Isao Inagaki
Mitsuru Seishima, MD, PhD
Takashi Deguchi, MD, PhD
spellingShingle Yoshiteru Yamada, PhD
Tomohiro Tsuchiya, MD, PhD
Isao Inagaki
Mitsuru Seishima, MD, PhD
Takashi Deguchi, MD, PhD
Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)
Transplantation Direct
author_facet Yoshiteru Yamada, PhD
Tomohiro Tsuchiya, MD, PhD
Isao Inagaki
Mitsuru Seishima, MD, PhD
Takashi Deguchi, MD, PhD
author_sort Yoshiteru Yamada, PhD
title Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)
title_short Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)
title_full Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)
title_fullStr Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)
title_full_unstemmed Prediction of Early BK Virus Infection in Kidney Transplant Recipients by the Number of Cells With Intranuclear Inclusion Bodies (Decoy Cells)
title_sort prediction of early bk virus infection in kidney transplant recipients by the number of cells with intranuclear inclusion bodies (decoy cells)
publisher Wolters Kluwer
series Transplantation Direct
issn 2373-8731
publishDate 2018-02-01
description Background. BK virus (BKV) is the cause of nephropathy. Because BKV nephropathy can progress to graft loss, early diagnosis of BKV infection is very important. In this study, we aimed to investigate the utility of quantifying cells with intranuclear inclusion bodies (decoy cells) in urinary sediment for the screening and monitoring of BKV infection in renal transplant recipients at our hospital. Methods. This was a retrospective single-center study. Urine sediment examination was performed at each outpatient visit, and the number of decoy cells was measured in the whole microscopic field. Patients (n = 41) were divided into the BK viremia group (blood positive for BKV DNA by polymerase chain reaction [PCR]) and non-BK viremia group (blood negative for BKV DNA by PCR), and the decoy cell count in urinary sediments was examined. Results. The maximum decoy cell count was significantly higher (P = 0.04) in the BK viremia group than in the non-BK viremia group. In the receiver operating characteristic curve for the maximum decoy cells, the cutoff value was 507 cells. The area under the receiver operating characteristic curve was 0.8774 (95% confidence interval, 0.7739-0.9810). The number of decoy cells at the time of appearance in the BK viremia group was not significantly different from that in the non-BK viremia group. However, the BK viremia group showed an increasing trend, whereas the non-BK viremia group showed a decreasing trend, in the number of decoy cells. There was a positive correlation between the number of decoy cells and the data from the urine BKV-DNA PCR quantification (correlation coefficient [r] = 0.74). Conclusions. Measurement of decoy cells in urinary sediments may predict early BKV infection, and if performed quickly, it may be useful for screening and continuous monitoring of BKV infection in renal transplant recipients.
url http://journals.lww.com/transplantationdirect/fulltext/10.1097/TXD.0000000000000759
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