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Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy
Since urine samples more directly reflect kidney alterations and damage than blood samples, we investigated whether urine anti-PLA(2)R antibody (uPLA(2)R-Ab) could be utilized similarly to serum anti-PLA(2)R antibody (sPLA(2)R-Ab) as a noninvasive biomarker of idiopathic membranous nephropathy (IMN)...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787499/ https://www.ncbi.nlm.nih.gov/pubmed/29416596 http://dx.doi.org/10.18632/oncotarget.19859 |
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author | Wang, Yu He, Yi-Xin Diao, Tian-Tian Wei, Shi-Yao Qi, Wen-Rui Wang, Cen-Cen Song, Shu-Min Bi, Min Li, Chun-Mei Zhang, Cai-Xia Hou, Yan-Pei Wei, Qiu-Ju Li, Bing |
author_facet | Wang, Yu He, Yi-Xin Diao, Tian-Tian Wei, Shi-Yao Qi, Wen-Rui Wang, Cen-Cen Song, Shu-Min Bi, Min Li, Chun-Mei Zhang, Cai-Xia Hou, Yan-Pei Wei, Qiu-Ju Li, Bing |
author_sort | Wang, Yu |
collection | PubMed |
description | Since urine samples more directly reflect kidney alterations and damage than blood samples, we investigated whether urine anti-PLA(2)R antibody (uPLA(2)R-Ab) could be utilized similarly to serum anti-PLA(2)R antibody (sPLA(2)R-Ab) as a noninvasive biomarker of idiopathic membranous nephropathy (IMN). In this study, we performed a qualitative analysis using an indirect immunofluorescence test (IIFT) and measured uPLA(2)R-Ab and sPLA(2)R-Ab concentrations using an enzyme-linked immunosorbent assay (ELISA) in 28 patients with biopsy-proven IMN and 12 patients with secondary membranous nephropathy (SMN). Overall, 64.3% (n=18) of patients with IMN had IIFT-positive sPLA(2)R-Ab, 67.9% (n=19) of patients with IMN had IIFT-positive uPLA(2)R-Ab, and none of the SMN patients had IIFT-positive sPLA(2)R-Ab or uPLA(2)R-Ab. The titers of the anti-PLA(2)R antibody from the IMN patients in the urine (10.72±22.24 RU/μmol, presented as uPLA(2)R-Ab/urine creatinine) and serum (107.36±140.93 RU/ml) were higher than those from the SMN patients (0.51±0.46 RU/μmol, 0.008±0.029 RU/ml, respectively, p<0.05). Statistical analyses indicated that there were positive correlations between uPLA(2)R-Ab and gPLA(2)R, sPLA(2)R-Ab or urinary protein and negative correlations between uPLA(2)R-Ab and serum albumin in patients with IMN. In conclusion, uPLA(2)R-Ab is a novel biomarker of IMN. sPLA(2)R-Ab combined with uPLA(2)R-Ab might be more helpful for diagnosis and activity in PLA(2)R associated MN. |
format | Online Article Text |
id | pubmed-5787499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57874992018-02-07 Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy Wang, Yu He, Yi-Xin Diao, Tian-Tian Wei, Shi-Yao Qi, Wen-Rui Wang, Cen-Cen Song, Shu-Min Bi, Min Li, Chun-Mei Zhang, Cai-Xia Hou, Yan-Pei Wei, Qiu-Ju Li, Bing Oncotarget Research Paper: Immunology Since urine samples more directly reflect kidney alterations and damage than blood samples, we investigated whether urine anti-PLA(2)R antibody (uPLA(2)R-Ab) could be utilized similarly to serum anti-PLA(2)R antibody (sPLA(2)R-Ab) as a noninvasive biomarker of idiopathic membranous nephropathy (IMN). In this study, we performed a qualitative analysis using an indirect immunofluorescence test (IIFT) and measured uPLA(2)R-Ab and sPLA(2)R-Ab concentrations using an enzyme-linked immunosorbent assay (ELISA) in 28 patients with biopsy-proven IMN and 12 patients with secondary membranous nephropathy (SMN). Overall, 64.3% (n=18) of patients with IMN had IIFT-positive sPLA(2)R-Ab, 67.9% (n=19) of patients with IMN had IIFT-positive uPLA(2)R-Ab, and none of the SMN patients had IIFT-positive sPLA(2)R-Ab or uPLA(2)R-Ab. The titers of the anti-PLA(2)R antibody from the IMN patients in the urine (10.72±22.24 RU/μmol, presented as uPLA(2)R-Ab/urine creatinine) and serum (107.36±140.93 RU/ml) were higher than those from the SMN patients (0.51±0.46 RU/μmol, 0.008±0.029 RU/ml, respectively, p<0.05). Statistical analyses indicated that there were positive correlations between uPLA(2)R-Ab and gPLA(2)R, sPLA(2)R-Ab or urinary protein and negative correlations between uPLA(2)R-Ab and serum albumin in patients with IMN. In conclusion, uPLA(2)R-Ab is a novel biomarker of IMN. sPLA(2)R-Ab combined with uPLA(2)R-Ab might be more helpful for diagnosis and activity in PLA(2)R associated MN. Impact Journals LLC 2017-08-03 /pmc/articles/PMC5787499/ /pubmed/29416596 http://dx.doi.org/10.18632/oncotarget.19859 Text en Copyright: © 2018 Wang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Immunology Wang, Yu He, Yi-Xin Diao, Tian-Tian Wei, Shi-Yao Qi, Wen-Rui Wang, Cen-Cen Song, Shu-Min Bi, Min Li, Chun-Mei Zhang, Cai-Xia Hou, Yan-Pei Wei, Qiu-Ju Li, Bing Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy |
title | Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy |
title_full | Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy |
title_fullStr | Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy |
title_full_unstemmed | Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy |
title_short | Urine anti-PLA2R antibody is a novel biomarker of idiopathic membranous nephropathy |
title_sort | urine anti-pla2r antibody is a novel biomarker of idiopathic membranous nephropathy |
topic | Research Paper: Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787499/ https://www.ncbi.nlm.nih.gov/pubmed/29416596 http://dx.doi.org/10.18632/oncotarget.19859 |
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