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Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease

Serum Golgi protein 73 (GP73) is a promising marker for significant fibrosis in adults. However, current diagnostic value of serum GP73 for liver fibrosis in children is unknown. To investigate the relationship between levels of serum GP73 and liver fibrosis in children, we measured serum GP73 in 86...

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Autores principales: Liu, Langli, Wang, Jianwen, Feng, Jiayan, Yao, Mingjie, Hao, Chenzhi, You, Yijie, Yan, Yanyan, Gong, Jingyu, Lu, Yi, Xie, Xinbao, Zhang, Meihong, Chen, Lian, Li, Tingting, Lu, Fengmin, Wang, Jian-She
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233211/
https://www.ncbi.nlm.nih.gov/pubmed/30425268
http://dx.doi.org/10.1038/s41598-018-34714-y
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author Liu, Langli
Wang, Jianwen
Feng, Jiayan
Yao, Mingjie
Hao, Chenzhi
You, Yijie
Yan, Yanyan
Gong, Jingyu
Lu, Yi
Xie, Xinbao
Zhang, Meihong
Chen, Lian
Li, Tingting
Lu, Fengmin
Wang, Jian-She
author_facet Liu, Langli
Wang, Jianwen
Feng, Jiayan
Yao, Mingjie
Hao, Chenzhi
You, Yijie
Yan, Yanyan
Gong, Jingyu
Lu, Yi
Xie, Xinbao
Zhang, Meihong
Chen, Lian
Li, Tingting
Lu, Fengmin
Wang, Jian-She
author_sort Liu, Langli
collection PubMed
description Serum Golgi protein 73 (GP73) is a promising marker for significant fibrosis in adults. However, current diagnostic value of serum GP73 for liver fibrosis in children is unknown. To investigate the relationship between levels of serum GP73 and liver fibrosis in children, we measured serum GP73 in 86 healthy controls and 183 patients with liver diseases using commercially available double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) kit. The value of serum GP73 in fibrosis stage assessment was compared with aspartate transaminase to platelet ratio index (APRI). We found that serum GP73 was decreasing with age in healthy controls, while it was increasing with the extent of inflammation and fibrosis in patients with liver diseases. Though area under the receiver operating curve (AUROC) of serum GP73 for diagnosing significant fibrosis was nearly equal to APRI (0.62 vs 0.64) in patients aged 3 years or older, AUROC for serum GP73 was superior to APRI (0.76 vs 0.67) in patients aged below 3 years, indicating that serum GP73 is comparable to APRI for diagnosing significant fibrosis in children.
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spelling pubmed-62332112018-11-28 Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease Liu, Langli Wang, Jianwen Feng, Jiayan Yao, Mingjie Hao, Chenzhi You, Yijie Yan, Yanyan Gong, Jingyu Lu, Yi Xie, Xinbao Zhang, Meihong Chen, Lian Li, Tingting Lu, Fengmin Wang, Jian-She Sci Rep Article Serum Golgi protein 73 (GP73) is a promising marker for significant fibrosis in adults. However, current diagnostic value of serum GP73 for liver fibrosis in children is unknown. To investigate the relationship between levels of serum GP73 and liver fibrosis in children, we measured serum GP73 in 86 healthy controls and 183 patients with liver diseases using commercially available double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) kit. The value of serum GP73 in fibrosis stage assessment was compared with aspartate transaminase to platelet ratio index (APRI). We found that serum GP73 was decreasing with age in healthy controls, while it was increasing with the extent of inflammation and fibrosis in patients with liver diseases. Though area under the receiver operating curve (AUROC) of serum GP73 for diagnosing significant fibrosis was nearly equal to APRI (0.62 vs 0.64) in patients aged 3 years or older, AUROC for serum GP73 was superior to APRI (0.76 vs 0.67) in patients aged below 3 years, indicating that serum GP73 is comparable to APRI for diagnosing significant fibrosis in children. Nature Publishing Group UK 2018-11-13 /pmc/articles/PMC6233211/ /pubmed/30425268 http://dx.doi.org/10.1038/s41598-018-34714-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Langli
Wang, Jianwen
Feng, Jiayan
Yao, Mingjie
Hao, Chenzhi
You, Yijie
Yan, Yanyan
Gong, Jingyu
Lu, Yi
Xie, Xinbao
Zhang, Meihong
Chen, Lian
Li, Tingting
Lu, Fengmin
Wang, Jian-She
Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease
title Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease
title_full Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease
title_fullStr Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease
title_full_unstemmed Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease
title_short Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease
title_sort serum golgi protein 73 is a marker comparable to apri for diagnosing significant fibrosis in children with liver disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6233211/
https://www.ncbi.nlm.nih.gov/pubmed/30425268
http://dx.doi.org/10.1038/s41598-018-34714-y
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