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Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia
AIM: To investigate serum urokinase-type plasminogen activator receptor (uPAR) and liver stiffness in biliary atresia (BA) and examine the correlation of circulating uPAR, liver stiffness, and clinical outcomes in postoperative BA children. METHODS: Eighty-five postKasai BA children and 24 control s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124719/ https://www.ncbi.nlm.nih.gov/pubmed/27957246 http://dx.doi.org/10.4254/wjh.v8.i33.1471 |
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author | Udomsinprasert, Wanvisa Honsawek, Sittisak Jirathanathornnukul, Napaphat Chongsrisawat, Voranush Poovorawan, Yong |
author_facet | Udomsinprasert, Wanvisa Honsawek, Sittisak Jirathanathornnukul, Napaphat Chongsrisawat, Voranush Poovorawan, Yong |
author_sort | Udomsinprasert, Wanvisa |
collection | PubMed |
description | AIM: To investigate serum urokinase-type plasminogen activator receptor (uPAR) and liver stiffness in biliary atresia (BA) and examine the correlation of circulating uPAR, liver stiffness, and clinical outcomes in postoperative BA children. METHODS: Eighty-five postKasai BA children and 24 control subjects were registered. Circulating uPAR was measured using enzyme-linked immunosorbent essay. Liver stiffness was analyzed using transient elastography. RESULTS: BA children had significantly greater circulating uPAR and liver stiffness scores than control subjects (P < 0.001). Circulating uPAR and liver stiffness were substantially higher in jaundiced BA children than non-jaundiced BA children (P < 0.001). In addition, circulating uPAR was positively associated with serum aspartate aminotransferase (r = 0.507, P < 0.001), alanine aminotransferase (r = 0.364, P < 0.001), total bilirubin (r = 0.559, P < 0.001), alkaline phosphatase (r = 0.325, P < 0.001), and liver stiffness scores (r = 0.508, P < 0.001). CONCLUSION: Circulating uPAR and liver stiffness values were greater in BA children than healthy controls. The increased circulating uPAR was associated with liver dysfunction in BA. As a consequence, serum uPAR and liver stiffness may be used as noninvasive biomarkers indicating the progression of liver fibrosis in postKasai BA. |
format | Online Article Text |
id | pubmed-5124719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-51247192016-12-12 Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia Udomsinprasert, Wanvisa Honsawek, Sittisak Jirathanathornnukul, Napaphat Chongsrisawat, Voranush Poovorawan, Yong World J Hepatol Prospective Study AIM: To investigate serum urokinase-type plasminogen activator receptor (uPAR) and liver stiffness in biliary atresia (BA) and examine the correlation of circulating uPAR, liver stiffness, and clinical outcomes in postoperative BA children. METHODS: Eighty-five postKasai BA children and 24 control subjects were registered. Circulating uPAR was measured using enzyme-linked immunosorbent essay. Liver stiffness was analyzed using transient elastography. RESULTS: BA children had significantly greater circulating uPAR and liver stiffness scores than control subjects (P < 0.001). Circulating uPAR and liver stiffness were substantially higher in jaundiced BA children than non-jaundiced BA children (P < 0.001). In addition, circulating uPAR was positively associated with serum aspartate aminotransferase (r = 0.507, P < 0.001), alanine aminotransferase (r = 0.364, P < 0.001), total bilirubin (r = 0.559, P < 0.001), alkaline phosphatase (r = 0.325, P < 0.001), and liver stiffness scores (r = 0.508, P < 0.001). CONCLUSION: Circulating uPAR and liver stiffness values were greater in BA children than healthy controls. The increased circulating uPAR was associated with liver dysfunction in BA. As a consequence, serum uPAR and liver stiffness may be used as noninvasive biomarkers indicating the progression of liver fibrosis in postKasai BA. Baishideng Publishing Group Inc 2016-11-28 2016-11-28 /pmc/articles/PMC5124719/ /pubmed/27957246 http://dx.doi.org/10.4254/wjh.v8.i33.1471 Text en ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Prospective Study Udomsinprasert, Wanvisa Honsawek, Sittisak Jirathanathornnukul, Napaphat Chongsrisawat, Voranush Poovorawan, Yong Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia |
title | Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia |
title_full | Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia |
title_fullStr | Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia |
title_full_unstemmed | Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia |
title_short | Elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia |
title_sort | elevation of serum urokinase plasminogen activator receptor and liver stiffness in postoperative biliary atresia |
topic | Prospective Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124719/ https://www.ncbi.nlm.nih.gov/pubmed/27957246 http://dx.doi.org/10.4254/wjh.v8.i33.1471 |
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