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Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis

BACKGROUND/AIMS: To date, studies on various noninvasive techniques have been suggested to evaluate the degree of liver fibrosis. We aimed to investigate the diagnostic performance of serum asialo α1-acid glycoprotein (AsAGP) in the diagnosis of liver cirrhosis compared with chronic hepatitis for cl...

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Autores principales: Lim, Dae Hyun, Kim, Mimi, Jun, Dae Won, Kwak, Min Jung, Yoon, Jai Hoon, Lee, Kang Nyeong, Lee, Hang Lak, Lee, Oh Young, Yoon, Byung Chul, Choi, Ho Soon, Kang, Bo Kyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817921/
https://www.ncbi.nlm.nih.gov/pubmed/32066208
http://dx.doi.org/10.5009/gnl19282
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author Lim, Dae Hyun
Kim, Mimi
Jun, Dae Won
Kwak, Min Jung
Yoon, Jai Hoon
Lee, Kang Nyeong
Lee, Hang Lak
Lee, Oh Young
Yoon, Byung Chul
Choi, Ho Soon
Kang, Bo Kyeong
author_facet Lim, Dae Hyun
Kim, Mimi
Jun, Dae Won
Kwak, Min Jung
Yoon, Jai Hoon
Lee, Kang Nyeong
Lee, Hang Lak
Lee, Oh Young
Yoon, Byung Chul
Choi, Ho Soon
Kang, Bo Kyeong
author_sort Lim, Dae Hyun
collection PubMed
description BACKGROUND/AIMS: To date, studies on various noninvasive techniques have been suggested to evaluate the degree of liver fibrosis. We aimed to investigate the diagnostic performance of serum asialo α1-acid glycoprotein (AsAGP) in the diagnosis of liver cirrhosis compared with chronic hepatitis for clinically useful result. METHODS: We conducted a case-control study of 96 patients with chronic liver disease. Chronic hepatitis was defined as the presence of chronic liver disease on ultrasonography, with a liver stiffness of less than 5.0 kPa as shown on magnetic resonance elastography (MRE). Liver cirrhosis was defined as liver stiffness of more than 5.0 kPa on MRE. The serum AsAGP concentration was compared between the two groups. RESULTS: Serum AsAGP levels were significantly higher in patients with cirrhosis than in those with chronic hepatitis (1.83 μg/mL vs 1.42 μg/mL, p<0.001). Additionally, when comparing patients in each cirrhotic group (Child-Pugh grades A, B, and C) to those with chronic hepatitis, AsAGP levels were significantly higher in all the cirrhotic groups (p<0.05, p<0.01, p<0.001, respectively). The sensitivity and specificity of AsAGP for detecting cirrhosis were 79.2% and 64.6%, respectively, and the area under the curve value was 0.733. The best diagnostic cutoff to predict cirrhosis was 1.4 μg/mL. AsAGP and bilirubin were found to be independent risk factors for the prediction of cirrhosis in the logistic regression analysis. CONCLUSIONS: Serum AsAGP showed an acceptable diagnostic performance in predicting liver cirrhosis.
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spelling pubmed-78179212021-01-29 Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis Lim, Dae Hyun Kim, Mimi Jun, Dae Won Kwak, Min Jung Yoon, Jai Hoon Lee, Kang Nyeong Lee, Hang Lak Lee, Oh Young Yoon, Byung Chul Choi, Ho Soon Kang, Bo Kyeong Gut Liver Original Article BACKGROUND/AIMS: To date, studies on various noninvasive techniques have been suggested to evaluate the degree of liver fibrosis. We aimed to investigate the diagnostic performance of serum asialo α1-acid glycoprotein (AsAGP) in the diagnosis of liver cirrhosis compared with chronic hepatitis for clinically useful result. METHODS: We conducted a case-control study of 96 patients with chronic liver disease. Chronic hepatitis was defined as the presence of chronic liver disease on ultrasonography, with a liver stiffness of less than 5.0 kPa as shown on magnetic resonance elastography (MRE). Liver cirrhosis was defined as liver stiffness of more than 5.0 kPa on MRE. The serum AsAGP concentration was compared between the two groups. RESULTS: Serum AsAGP levels were significantly higher in patients with cirrhosis than in those with chronic hepatitis (1.83 μg/mL vs 1.42 μg/mL, p<0.001). Additionally, when comparing patients in each cirrhotic group (Child-Pugh grades A, B, and C) to those with chronic hepatitis, AsAGP levels were significantly higher in all the cirrhotic groups (p<0.05, p<0.01, p<0.001, respectively). The sensitivity and specificity of AsAGP for detecting cirrhosis were 79.2% and 64.6%, respectively, and the area under the curve value was 0.733. The best diagnostic cutoff to predict cirrhosis was 1.4 μg/mL. AsAGP and bilirubin were found to be independent risk factors for the prediction of cirrhosis in the logistic regression analysis. CONCLUSIONS: Serum AsAGP showed an acceptable diagnostic performance in predicting liver cirrhosis. Editorial Office of Gut and Liver 2021-01-15 2020-02-20 /pmc/articles/PMC7817921/ /pubmed/32066208 http://dx.doi.org/10.5009/gnl19282 Text en Copyright © Gut and Liver. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lim, Dae Hyun
Kim, Mimi
Jun, Dae Won
Kwak, Min Jung
Yoon, Jai Hoon
Lee, Kang Nyeong
Lee, Hang Lak
Lee, Oh Young
Yoon, Byung Chul
Choi, Ho Soon
Kang, Bo Kyeong
Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis
title Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis
title_full Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis
title_fullStr Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis
title_full_unstemmed Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis
title_short Diagnostic Performance of Serum Asialo α(1)-Acid Glycoprotein Levels to Predict Liver Cirrhosis
title_sort diagnostic performance of serum asialo α(1)-acid glycoprotein levels to predict liver cirrhosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817921/
https://www.ncbi.nlm.nih.gov/pubmed/32066208
http://dx.doi.org/10.5009/gnl19282
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