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Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism

BACKGROUND: Non-alcoholic steatohepatitis (NASH) is a progressive form of non-alcoholic fatty liver disease (NAFLD). The diagnostic gold standard for detecting NASH still relies upon an invasive pathological biopsy. There is, therefore, a need to identify non-invasive diagnostic markers. Oxidative s...

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Autores principales: Xia, Ziqiang, Hu, Mei, Zheng, Liang, Zheng, Endian, Deng, Min, Wu, Jinming, Sheng, Xiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Medical Biochemists of Serbia, Belgrade 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9921090/
https://www.ncbi.nlm.nih.gov/pubmed/36819130
http://dx.doi.org/10.5937/jomb0-37597
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author Xia, Ziqiang
Hu, Mei
Zheng, Liang
Zheng, Endian
Deng, Min
Wu, Jinming
Sheng, Xiong
author_facet Xia, Ziqiang
Hu, Mei
Zheng, Liang
Zheng, Endian
Deng, Min
Wu, Jinming
Sheng, Xiong
author_sort Xia, Ziqiang
collection PubMed
description BACKGROUND: Non-alcoholic steatohepatitis (NASH) is a progressive form of non-alcoholic fatty liver disease (NAFLD). The diagnostic gold standard for detecting NASH still relies upon an invasive pathological biopsy. There is, therefore, a need to identify non-invasive diagnostic markers. Oxidative stress mediates fatty liver progression to NASH. Imbalanced iron metabolism produces many reactive oxygen species (ROS). Ceruloplasmin is associated with oxidase and iron metabolism-related activities. The current study aimed to determine whether there was a correlation between ceruloplasmin levels and NASH and whether such a relationship may be associated with altered iron metabolism in NASH patients. METHODS: A total of 135 NAFLD patients were enrolled in this study. A pathological biopsy confirmed that 60 of those patients had NAFLD activity scores (NAS) 5, while the remaining 75 had NAS<5. RESULTS: Receiver operating characteristic (ROC) curves confirmed that serum ceruloplasmin and ferritin levels were predictors of NAS 5 and NAS<5, with area under the curve (AUC) values of 0.80 and 0.81, respectively. The serum ceruloplasmin levels in NAS 5 patients were significantly lower than those in NAS<5 patients (p< 0.001). Serum ceruloplasmin levels were also negatively correlated with ferritin levels. Lower serum ceruloplasmin levels were associated with more severe histopathological findings. CONCLUSIONS: Low serum ceruloplasmin and high serum ferritin are correlated with NASH. A high concentration of serum ferritin is a viable clinical biomarker of NASH, and low serum ceruloplasmin may participate in the occurrence of NASH by regulating iron load, which can be used as a non-invasive diagnostic marker of NASH.
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spelling pubmed-99210902023-02-16 Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism Xia, Ziqiang Hu, Mei Zheng, Liang Zheng, Endian Deng, Min Wu, Jinming Sheng, Xiong J Med Biochem Original Paper BACKGROUND: Non-alcoholic steatohepatitis (NASH) is a progressive form of non-alcoholic fatty liver disease (NAFLD). The diagnostic gold standard for detecting NASH still relies upon an invasive pathological biopsy. There is, therefore, a need to identify non-invasive diagnostic markers. Oxidative stress mediates fatty liver progression to NASH. Imbalanced iron metabolism produces many reactive oxygen species (ROS). Ceruloplasmin is associated with oxidase and iron metabolism-related activities. The current study aimed to determine whether there was a correlation between ceruloplasmin levels and NASH and whether such a relationship may be associated with altered iron metabolism in NASH patients. METHODS: A total of 135 NAFLD patients were enrolled in this study. A pathological biopsy confirmed that 60 of those patients had NAFLD activity scores (NAS) 5, while the remaining 75 had NAS<5. RESULTS: Receiver operating characteristic (ROC) curves confirmed that serum ceruloplasmin and ferritin levels were predictors of NAS 5 and NAS<5, with area under the curve (AUC) values of 0.80 and 0.81, respectively. The serum ceruloplasmin levels in NAS 5 patients were significantly lower than those in NAS<5 patients (p< 0.001). Serum ceruloplasmin levels were also negatively correlated with ferritin levels. Lower serum ceruloplasmin levels were associated with more severe histopathological findings. CONCLUSIONS: Low serum ceruloplasmin and high serum ferritin are correlated with NASH. A high concentration of serum ferritin is a viable clinical biomarker of NASH, and low serum ceruloplasmin may participate in the occurrence of NASH by regulating iron load, which can be used as a non-invasive diagnostic marker of NASH. Society of Medical Biochemists of Serbia, Belgrade 2023-01-20 2023-01-20 /pmc/articles/PMC9921090/ /pubmed/36819130 http://dx.doi.org/10.5937/jomb0-37597 Text en 2023 Ziqiang Xia, Mei Hu, Liang Zheng, Endian Zheng, Min Deng, Jinming Wu, Xiong Sheng, published by CEON/CEES https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 License.
spellingShingle Original Paper
Xia, Ziqiang
Hu, Mei
Zheng, Liang
Zheng, Endian
Deng, Min
Wu, Jinming
Sheng, Xiong
Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism
title Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism
title_full Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism
title_fullStr Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism
title_full_unstemmed Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism
title_short Assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism
title_sort assessing whether serum ceruloplasmin promotes non-alcoholic steatohepatitis via regulating iron metabolism
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9921090/
https://www.ncbi.nlm.nih.gov/pubmed/36819130
http://dx.doi.org/10.5937/jomb0-37597
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