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Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy
Background: This investigation was managed to explore whether miR-193a in combination with two podocytes, namely, Wilms tumor type 1 (WT1) and podocalyxin (PODXL), were feasible in estimating onset and prognosis of idiopathic membranous nephropathy (IMN). Methods: We recruited a total of 189 healthy...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711109/ https://www.ncbi.nlm.nih.gov/pubmed/31352863 http://dx.doi.org/10.1080/0886022X.2019.1642210 |
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author | Zhang, Wei Ren, Yeping Li, Jie |
author_facet | Zhang, Wei Ren, Yeping Li, Jie |
author_sort | Zhang, Wei |
collection | PubMed |
description | Background: This investigation was managed to explore whether miR-193a in combination with two podocytes, namely, Wilms tumor type 1 (WT1) and podocalyxin (PODXL), were feasible in estimating onset and prognosis of idiopathic membranous nephropathy (IMN). Methods: We recruited a total of 189 healthy controls and 364 IMN patients, whose urine samples were prepared to measure the expression of miR-193a and PODXL. Meanwhile, renal tissues collected from above-mentioned IMN patients (n = 364) and renal cell carcinoma patients (n = 189) were arranged to determine the expression of WT1. Ultimately, receiver operating characteristic curves were constructed to appraise the performance of miR-193a, WT1, and PODXL in predicting renal survival of IMN patients. Results: The IMN patients were measured with up-regulated miR-193a expression and down-regulated WT1/PODXL expression, when compared with healthy controls (p < 0.05). Moreover, highly expressed miR-193a, lowly expressed WT1/PODXL, elevated amounts of proteinuria (>3.79 g/24 h)/serum creatinine (>174.63 μmol/L), and declined GFR (≤68.13 mL/min/1.73 m(2)) were implicated as prominent biomarkers for the poor renal survival of IMN patients (all p < 0.05). Notably, miR-193a combined with PODXL and WT1 generated optimal effects in differentiating IMN patients from healthy controls (AUC = 0.994) and also in anticipating the renal survival state of IMN patients (AUC = 0.824), when compared with strategies that merely employed ≤2 of the biomarkers. Conclusion: The combination of miR-193a, WT1, and PODXL might serve as a favorable strategy for expecting IMN prognosis. |
format | Online Article Text |
id | pubmed-6711109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-67111092019-09-05 Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy Zhang, Wei Ren, Yeping Li, Jie Ren Fail Clinical Study Background: This investigation was managed to explore whether miR-193a in combination with two podocytes, namely, Wilms tumor type 1 (WT1) and podocalyxin (PODXL), were feasible in estimating onset and prognosis of idiopathic membranous nephropathy (IMN). Methods: We recruited a total of 189 healthy controls and 364 IMN patients, whose urine samples were prepared to measure the expression of miR-193a and PODXL. Meanwhile, renal tissues collected from above-mentioned IMN patients (n = 364) and renal cell carcinoma patients (n = 189) were arranged to determine the expression of WT1. Ultimately, receiver operating characteristic curves were constructed to appraise the performance of miR-193a, WT1, and PODXL in predicting renal survival of IMN patients. Results: The IMN patients were measured with up-regulated miR-193a expression and down-regulated WT1/PODXL expression, when compared with healthy controls (p < 0.05). Moreover, highly expressed miR-193a, lowly expressed WT1/PODXL, elevated amounts of proteinuria (>3.79 g/24 h)/serum creatinine (>174.63 μmol/L), and declined GFR (≤68.13 mL/min/1.73 m(2)) were implicated as prominent biomarkers for the poor renal survival of IMN patients (all p < 0.05). Notably, miR-193a combined with PODXL and WT1 generated optimal effects in differentiating IMN patients from healthy controls (AUC = 0.994) and also in anticipating the renal survival state of IMN patients (AUC = 0.824), when compared with strategies that merely employed ≤2 of the biomarkers. Conclusion: The combination of miR-193a, WT1, and PODXL might serve as a favorable strategy for expecting IMN prognosis. Taylor & Francis 2019-07-29 /pmc/articles/PMC6711109/ /pubmed/31352863 http://dx.doi.org/10.1080/0886022X.2019.1642210 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Zhang, Wei Ren, Yeping Li, Jie Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy |
title | Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy |
title_full | Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy |
title_fullStr | Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy |
title_full_unstemmed | Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy |
title_short | Application of miR-193a/WT1/PODXL axis to estimate risk and prognosis of idiopathic membranous nephropathy |
title_sort | application of mir-193a/wt1/podxl axis to estimate risk and prognosis of idiopathic membranous nephropathy |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6711109/ https://www.ncbi.nlm.nih.gov/pubmed/31352863 http://dx.doi.org/10.1080/0886022X.2019.1642210 |
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