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Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis

AIM: To investigate the usefulness of aspartate aminotransferase to platelet ratio index (APRI) in predicting hepatocellular carcinoma (HCC) risk in primary biliary cholangitis (PBC). METHODS: We identified PBC patients between 2000 and 2015 by searching the electronic medical database of a tertiary...

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Autores principales: Cheung, Ka-Shing, Seto, Wai-Kay, Fung, James, Mak, Lung-Yi, Lai, Ching-Lung, Yuen, Man-Fung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703915/
https://www.ncbi.nlm.nih.gov/pubmed/29209127
http://dx.doi.org/10.3748/wjg.v23.i44.7863
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author Cheung, Ka-Shing
Seto, Wai-Kay
Fung, James
Mak, Lung-Yi
Lai, Ching-Lung
Yuen, Man-Fung
author_facet Cheung, Ka-Shing
Seto, Wai-Kay
Fung, James
Mak, Lung-Yi
Lai, Ching-Lung
Yuen, Man-Fung
author_sort Cheung, Ka-Shing
collection PubMed
description AIM: To investigate the usefulness of aspartate aminotransferase to platelet ratio index (APRI) in predicting hepatocellular carcinoma (HCC) risk in primary biliary cholangitis (PBC). METHODS: We identified PBC patients between 2000 and 2015 by searching the electronic medical database of a tertiary center. The hazard ratio (HR) of HCC with different risk factors was determined by Cox proportional hazards model. RESULTS: One hundred and forty-four PBC patients were recruited. Patients were diagnosed at a median age of 57.8 years [interquartile range (IQR): 48.7-71.5 years), and 41 (28.5%) patients had cirrhosis at baseline. The median follow-up duration was 6.9 years (range: 1.0-26.3 years). Twelve patients developed HCC, with an incidence rate of 10.6 cases per 1000 patient-years. The overall 5-, 10- and 15-year cumulative incidences of HCC were 2.3% 95%CI: 0%-4.8%), 8.4% (95%CI: 1.8%-14.5%) and 21.6% (6.8%-34.1%), respectively. Older age (HR = 1.07), cirrhosis (HR = 4.38) and APRI at 1 year after treatment (APRI-r1) > 0.54 (HR = 3.94) were independent factors for HCC development. APRI-r1, when combined with treatment response, further stratified HCC risk (log rank P < 0.05). The area under receiver operating curve of APRI-r1 in predicting HCC was 0.77 (95%CI: 0.64-0.88). CONCLUSION: APRI-r1 can be used to predict the development of HCC in PBC patients. Combination of APRI-r1 with treatment response can further stratify the HCC risk.
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spelling pubmed-57039152017-12-05 Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis Cheung, Ka-Shing Seto, Wai-Kay Fung, James Mak, Lung-Yi Lai, Ching-Lung Yuen, Man-Fung World J Gastroenterol Retrospective Study AIM: To investigate the usefulness of aspartate aminotransferase to platelet ratio index (APRI) in predicting hepatocellular carcinoma (HCC) risk in primary biliary cholangitis (PBC). METHODS: We identified PBC patients between 2000 and 2015 by searching the electronic medical database of a tertiary center. The hazard ratio (HR) of HCC with different risk factors was determined by Cox proportional hazards model. RESULTS: One hundred and forty-four PBC patients were recruited. Patients were diagnosed at a median age of 57.8 years [interquartile range (IQR): 48.7-71.5 years), and 41 (28.5%) patients had cirrhosis at baseline. The median follow-up duration was 6.9 years (range: 1.0-26.3 years). Twelve patients developed HCC, with an incidence rate of 10.6 cases per 1000 patient-years. The overall 5-, 10- and 15-year cumulative incidences of HCC were 2.3% 95%CI: 0%-4.8%), 8.4% (95%CI: 1.8%-14.5%) and 21.6% (6.8%-34.1%), respectively. Older age (HR = 1.07), cirrhosis (HR = 4.38) and APRI at 1 year after treatment (APRI-r1) > 0.54 (HR = 3.94) were independent factors for HCC development. APRI-r1, when combined with treatment response, further stratified HCC risk (log rank P < 0.05). The area under receiver operating curve of APRI-r1 in predicting HCC was 0.77 (95%CI: 0.64-0.88). CONCLUSION: APRI-r1 can be used to predict the development of HCC in PBC patients. Combination of APRI-r1 with treatment response can further stratify the HCC risk. Baishideng Publishing Group Inc 2017-11-28 2017-11-28 /pmc/articles/PMC5703915/ /pubmed/29209127 http://dx.doi.org/10.3748/wjg.v23.i44.7863 Text en ©The Author(s) 2017. 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 Retrospective Study
Cheung, Ka-Shing
Seto, Wai-Kay
Fung, James
Mak, Lung-Yi
Lai, Ching-Lung
Yuen, Man-Fung
Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
title Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
title_full Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
title_fullStr Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
title_full_unstemmed Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
title_short Prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
title_sort prediction of hepatocellular carcinoma development by aminotransferase to platelet ratio index in primary biliary cholangitis
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703915/
https://www.ncbi.nlm.nih.gov/pubmed/29209127
http://dx.doi.org/10.3748/wjg.v23.i44.7863
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