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Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction
BACKGROUND: Post-transplant infection with polyoma viruses (BK and JC viruses) is an important cause of graft loss and nephropathy. The objective of this study was to compare the frequency of BK and JC viruria in renal transplant recipients with and without graft dysfunction. METHODS: In a case-cont...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263105/ https://www.ncbi.nlm.nih.gov/pubmed/22279460 |
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author | Taheri, Shahram Kafilzadeh, Farshid Shafa, Maryam Yaran, Majid Mortazavi, Mojgan Seirafian, Shiva Shahidi, Shahrzad Atapour, Abdolamir |
author_facet | Taheri, Shahram Kafilzadeh, Farshid Shafa, Maryam Yaran, Majid Mortazavi, Mojgan Seirafian, Shiva Shahidi, Shahrzad Atapour, Abdolamir |
author_sort | Taheri, Shahram |
collection | PubMed |
description | BACKGROUND: Post-transplant infection with polyoma viruses (BK and JC viruses) is an important cause of graft loss and nephropathy. The objective of this study was to compare the frequency of BK and JC viruria in renal transplant recipients with and without graft dysfunction. METHODS: In a case-control study, we selected 60 kidney transplant patients with and without graft dysfunction in the first two years after transplantation. Each group consisted of 30 patients evaluated for basic demographic and laboratory characteristics. First morning urine samples were sent for BK and JC virus detection with QIAamp DNA Mini Kit and real-time polymerase PCR. Chi-square test with Yates’ correction, Student t-test and Mann-Whitney U test were used as indicated. P value of less than 0.05 was regarded as statistically significant. RESULTS: Both groups were similar in age, gender, and time after transplant and pretransplant dialysis. In both groups, seven patients (23.3%) were JC virus positive whereas in case group 14 patients (46.7%) and in control group 9 patients (30%) were BK virus positive. There were no statistical significant difference between case and control groups for both JC and BK virus infection rate. CONCLUSIONS: We concluded that JC and BK virus infection is very prevalent in the first 2 years after transplant and might be monitored appropriately. |
format | Online Article Text |
id | pubmed-3263105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32631052012-01-25 Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction Taheri, Shahram Kafilzadeh, Farshid Shafa, Maryam Yaran, Majid Mortazavi, Mojgan Seirafian, Shiva Shahidi, Shahrzad Atapour, Abdolamir J Res Med Sci Original Article BACKGROUND: Post-transplant infection with polyoma viruses (BK and JC viruses) is an important cause of graft loss and nephropathy. The objective of this study was to compare the frequency of BK and JC viruria in renal transplant recipients with and without graft dysfunction. METHODS: In a case-control study, we selected 60 kidney transplant patients with and without graft dysfunction in the first two years after transplantation. Each group consisted of 30 patients evaluated for basic demographic and laboratory characteristics. First morning urine samples were sent for BK and JC virus detection with QIAamp DNA Mini Kit and real-time polymerase PCR. Chi-square test with Yates’ correction, Student t-test and Mann-Whitney U test were used as indicated. P value of less than 0.05 was regarded as statistically significant. RESULTS: Both groups were similar in age, gender, and time after transplant and pretransplant dialysis. In both groups, seven patients (23.3%) were JC virus positive whereas in case group 14 patients (46.7%) and in control group 9 patients (30%) were BK virus positive. There were no statistical significant difference between case and control groups for both JC and BK virus infection rate. CONCLUSIONS: We concluded that JC and BK virus infection is very prevalent in the first 2 years after transplant and might be monitored appropriately. Medknow Publications & Media Pvt Ltd 2011-07 /pmc/articles/PMC3263105/ /pubmed/22279460 Text en Copyright: © Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Taheri, Shahram Kafilzadeh, Farshid Shafa, Maryam Yaran, Majid Mortazavi, Mojgan Seirafian, Shiva Shahidi, Shahrzad Atapour, Abdolamir Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction |
title | Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction |
title_full | Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction |
title_fullStr | Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction |
title_full_unstemmed | Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction |
title_short | Comparison of polyomavirus (BK virus and JC viruses) viruria in renal transplant recipients with and without kidney dysfunction |
title_sort | comparison of polyomavirus (bk virus and jc viruses) viruria in renal transplant recipients with and without kidney dysfunction |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263105/ https://www.ncbi.nlm.nih.gov/pubmed/22279460 |
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