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Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value?
AIM OF THE STUDY: We aimed to assess the utility of serum level IL-13Rα2 receptors as a non-invasive marker for early diagnosis of biliary atresia (BA) and selection of BA patients indicated for Kasai portoenterostomy. MATERIAL AND METHODS: The study included 60 infants with neonatal cholestasis in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000744/ https://www.ncbi.nlm.nih.gov/pubmed/29904725 http://dx.doi.org/10.5114/ceh.2018.75958 |
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author | Adawy, Nermin El-Araby, Hanaa Allam, Alif Elshenawy, Soha Khedr, Mohammed Ibrahim, Yasmine Zakaria, Haidy M. |
author_facet | Adawy, Nermin El-Araby, Hanaa Allam, Alif Elshenawy, Soha Khedr, Mohammed Ibrahim, Yasmine Zakaria, Haidy M. |
author_sort | Adawy, Nermin |
collection | PubMed |
description | AIM OF THE STUDY: We aimed to assess the utility of serum level IL-13Rα2 receptors as a non-invasive marker for early diagnosis of biliary atresia (BA) and selection of BA patients indicated for Kasai portoenterostomy. MATERIAL AND METHODS: The study included 60 infants with neonatal cholestasis in three groups; early BA group (n = 20), delayed BA group (n = 20) and non-BA cholestasis group (n = 20). A fourth group of 20 healthy neonates (n = 20) served as controls. IL-13Rα2 was measured by enzyme-linked immunosorbent assay in all patients and controls. RESULTS: The mean value of IL-13Rα2 was significantly higher in delayed BA group (11.05 ± 10.9 ng/ml) compared to early BA (0.34 ± 0.37 ng/ml), non-BA (0.54 ± 0.85 ng/ml) and control (0.24-0.2 ng/ml) groups. The levels of serum IL-13Rα2 increase with the severity of the degree of fibrosis. IL-13Rα2 at a cutoff level > 0.782 ng/ml could predict late fibrosis with accuracy of 77.55% (p < 0.0001). IL-13Rα2 could differentiate between preserved and disturbed liver architecture at a cut off value of more than 0.42 ng/ml with an accuracy of 81.6%. CONCLUSIONS: Serum IL-13Rα2 not a diagnostic marker for BA however it could be used as a noninvasive marker for detection of advanced liver fibrosis and presence of disturbed liver architecture that helps in patient selection for undergoing Kasai operation. Serum IL-13Rα2 could be a future therapeutic target for management of BA patients and any fibrotic liver disease. |
format | Online Article Text |
id | pubmed-6000744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-60007442018-06-14 Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? Adawy, Nermin El-Araby, Hanaa Allam, Alif Elshenawy, Soha Khedr, Mohammed Ibrahim, Yasmine Zakaria, Haidy M. Clin Exp Hepatol Original Paper AIM OF THE STUDY: We aimed to assess the utility of serum level IL-13Rα2 receptors as a non-invasive marker for early diagnosis of biliary atresia (BA) and selection of BA patients indicated for Kasai portoenterostomy. MATERIAL AND METHODS: The study included 60 infants with neonatal cholestasis in three groups; early BA group (n = 20), delayed BA group (n = 20) and non-BA cholestasis group (n = 20). A fourth group of 20 healthy neonates (n = 20) served as controls. IL-13Rα2 was measured by enzyme-linked immunosorbent assay in all patients and controls. RESULTS: The mean value of IL-13Rα2 was significantly higher in delayed BA group (11.05 ± 10.9 ng/ml) compared to early BA (0.34 ± 0.37 ng/ml), non-BA (0.54 ± 0.85 ng/ml) and control (0.24-0.2 ng/ml) groups. The levels of serum IL-13Rα2 increase with the severity of the degree of fibrosis. IL-13Rα2 at a cutoff level > 0.782 ng/ml could predict late fibrosis with accuracy of 77.55% (p < 0.0001). IL-13Rα2 could differentiate between preserved and disturbed liver architecture at a cut off value of more than 0.42 ng/ml with an accuracy of 81.6%. CONCLUSIONS: Serum IL-13Rα2 not a diagnostic marker for BA however it could be used as a noninvasive marker for detection of advanced liver fibrosis and presence of disturbed liver architecture that helps in patient selection for undergoing Kasai operation. Serum IL-13Rα2 could be a future therapeutic target for management of BA patients and any fibrotic liver disease. Termedia Publishing House 2018-05-25 2018-06 /pmc/articles/PMC6000744/ /pubmed/29904725 http://dx.doi.org/10.5114/ceh.2018.75958 Text en Copyright: © 2018 Clinical and Experimental Hepatology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Paper Adawy, Nermin El-Araby, Hanaa Allam, Alif Elshenawy, Soha Khedr, Mohammed Ibrahim, Yasmine Zakaria, Haidy M. Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? |
title | Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? |
title_full | Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? |
title_fullStr | Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? |
title_full_unstemmed | Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? |
title_short | Serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? |
title_sort | serum level of interleukin-13 receptor alpha 2 in infants with biliary atresia – is it of value? |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000744/ https://www.ncbi.nlm.nih.gov/pubmed/29904725 http://dx.doi.org/10.5114/ceh.2018.75958 |
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