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The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome
The aim of this study is to investigate whether Syndecan-1 (SDC-1), an indicator of endothelial glycocalyx injury, would increase the risk of hypercoagulable state and thrombosis in patients with nephrotic syndrome (NS). The prospective study was conducted among patients undergoing renal biopsy in t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114750/ https://www.ncbi.nlm.nih.gov/pubmed/33942670 http://dx.doi.org/10.1177/10760296211010256 |
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author | Chen, Xin Geng, Xuemei Jin, Shi Xu, Jiarui Guo, Man Shen, Daoqi Ding, Xiaoqiang Liu, Hong Xu, Xialian |
author_facet | Chen, Xin Geng, Xuemei Jin, Shi Xu, Jiarui Guo, Man Shen, Daoqi Ding, Xiaoqiang Liu, Hong Xu, Xialian |
author_sort | Chen, Xin |
collection | PubMed |
description | The aim of this study is to investigate whether Syndecan-1 (SDC-1), an indicator of endothelial glycocalyx injury, would increase the risk of hypercoagulable state and thrombosis in patients with nephrotic syndrome (NS). The prospective study was conducted among patients undergoing renal biopsy in the Department of Nephrology in our hospital from May to September 2018. We enrolled in patients with NS as the experimental group and patients with normal serum creatinine and proteinuria less than 1 g as the control group. Patients’ characteristics including age, sex, laboratory test results and blood samples were collected for each patient. The blood samples were taken before the renal biopsy. The samples were immediately processed and frozen at −80°C for later measurement of Syndecan-1. One hundred and thirty-six patients were enrolled in the study. Patients with NS and hypercoagulability had a higher level of SDC-1 compared with control group. Patients with membranous nephropathy occupied the highest SDC-1 level (P = 0.012). Logistic regression showed that highly increased level of SDC-1 (>53.18 ng/ml) was an independent predicator for predicting hypercoagulable state. The elevated level of SDC-1 indicated that endothelial injury, combined with its role of accelerating hypercoagulable state, might be considered of vital importance in the pathophysiological progress of thrombosis formation in patients with NS. |
format | Online Article Text |
id | pubmed-8114750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-81147502021-05-19 The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome Chen, Xin Geng, Xuemei Jin, Shi Xu, Jiarui Guo, Man Shen, Daoqi Ding, Xiaoqiang Liu, Hong Xu, Xialian Clin Appl Thromb Hemost Biomarkers for Evaluating the Risk and Prognosis of Vascular Diseases The aim of this study is to investigate whether Syndecan-1 (SDC-1), an indicator of endothelial glycocalyx injury, would increase the risk of hypercoagulable state and thrombosis in patients with nephrotic syndrome (NS). The prospective study was conducted among patients undergoing renal biopsy in the Department of Nephrology in our hospital from May to September 2018. We enrolled in patients with NS as the experimental group and patients with normal serum creatinine and proteinuria less than 1 g as the control group. Patients’ characteristics including age, sex, laboratory test results and blood samples were collected for each patient. The blood samples were taken before the renal biopsy. The samples were immediately processed and frozen at −80°C for later measurement of Syndecan-1. One hundred and thirty-six patients were enrolled in the study. Patients with NS and hypercoagulability had a higher level of SDC-1 compared with control group. Patients with membranous nephropathy occupied the highest SDC-1 level (P = 0.012). Logistic regression showed that highly increased level of SDC-1 (>53.18 ng/ml) was an independent predicator for predicting hypercoagulable state. The elevated level of SDC-1 indicated that endothelial injury, combined with its role of accelerating hypercoagulable state, might be considered of vital importance in the pathophysiological progress of thrombosis formation in patients with NS. SAGE Publications 2021-05-04 /pmc/articles/PMC8114750/ /pubmed/33942670 http://dx.doi.org/10.1177/10760296211010256 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Biomarkers for Evaluating the Risk and Prognosis of Vascular Diseases Chen, Xin Geng, Xuemei Jin, Shi Xu, Jiarui Guo, Man Shen, Daoqi Ding, Xiaoqiang Liu, Hong Xu, Xialian The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome |
title | The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome |
title_full | The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome |
title_fullStr | The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome |
title_full_unstemmed | The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome |
title_short | The Association of Syndecan-1, Hypercoagulable State and Thrombosis and in Patients With Nephrotic Syndrome |
title_sort | association of syndecan-1, hypercoagulable state and thrombosis and in patients with nephrotic syndrome |
topic | Biomarkers for Evaluating the Risk and Prognosis of Vascular Diseases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114750/ https://www.ncbi.nlm.nih.gov/pubmed/33942670 http://dx.doi.org/10.1177/10760296211010256 |
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