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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Wolters Kluwer
2018-02-01
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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 |
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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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