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Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C

AIMS: Long-term risk stratification using combined liver stiffness (LS) and clinically relevant blood tests acquired at the baseline further beyond the sustained virologic response (SVR) visit for chronic hepatitis C (CHC) has not been thoroughly investigated. This study retrospectively investigated...

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Autores principales: Chen, Sheng-Hung, Lai, Hsueh-Chou, Su, Wen-Pang, Kao, Jung-Ta, Chuang, Po-Heng, Hsu, Wei-Fan, Wang, Hung-Wei, Hsieh, Tsung-Lin, Chen, Hung-Yao, Peng, Cheng-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273470/
https://www.ncbi.nlm.nih.gov/pubmed/35837486
http://dx.doi.org/10.1155/2022/5201443
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author Chen, Sheng-Hung
Lai, Hsueh-Chou
Su, Wen-Pang
Kao, Jung-Ta
Chuang, Po-Heng
Hsu, Wei-Fan
Wang, Hung-Wei
Hsieh, Tsung-Lin
Chen, Hung-Yao
Peng, Cheng-Yuan
author_facet Chen, Sheng-Hung
Lai, Hsueh-Chou
Su, Wen-Pang
Kao, Jung-Ta
Chuang, Po-Heng
Hsu, Wei-Fan
Wang, Hung-Wei
Hsieh, Tsung-Lin
Chen, Hung-Yao
Peng, Cheng-Yuan
author_sort Chen, Sheng-Hung
collection PubMed
description AIMS: Long-term risk stratification using combined liver stiffness (LS) and clinically relevant blood tests acquired at the baseline further beyond the sustained virologic response (SVR) visit for chronic hepatitis C (CHC) has not been thoroughly investigated. This study retrospectively investigated the prognostics of liver-related events (LREs) further beyond the SVR visit. METHODS: Cox regression and random forest models identified the key factors, including longitudinal LS and noninvasive test results, that could predict LREs, including hepatocellular carcinoma, during prespecified follow-ups from 2010 to 2021. Kaplan–Meier survival analysis estimated the significance of between-group risk stratification. RESULTS: Of the entire eligible cohort (n = 520) of CHC patients with SVR to antiviral therapy, 28 (5.4%) patients developed post-SVR LREs over a median follow-up period of 6.1 years (interquartile range = 3.5–8.7). The multivariate Cox regression analysis identified two significant predictors of LREs after the year 3 post-SVR (Y3PSVR) baseline (LRE, n = 15 of 28, 53.6%, median follow-up = 4.1 [1.6–6.4] years after Y3PSVR): LS at Y3PSVR (adjusted hazard ratio [aHR] = 3.980, 95% confidence interval [CI] = 2.085–7.597, P < 0.001), and α-fetoprotein (AFP) at Y3PSVR (aHR = 1.017, 95% CI = 1.001–1.034, P=0.034). LS ≥1.45 m/s and AFP ≥3.00 ng/mL for Y3PSVR yielded positive likelihood ratios of 4.24 and 2.62, respectively. Kaplan–Meier analysis revealed that among the stratified subgroups, the subgroup with concurrent LS ≥1.45 m/s and AFP ≥3.00 ng/mL at Y3PSVR exhibited the highest risk of LREs after Y3PSVR (log-rank P < 0.001). CONCLUSION: We recommend the combined use of concurrent LS and AFP in future prediction models for LREs in CHC. Patients with concurrently high LS and AFP values further beyond the SVR visit may require a recall policy involving intense surveillance.
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spelling pubmed-92734702022-07-13 Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C Chen, Sheng-Hung Lai, Hsueh-Chou Su, Wen-Pang Kao, Jung-Ta Chuang, Po-Heng Hsu, Wei-Fan Wang, Hung-Wei Hsieh, Tsung-Lin Chen, Hung-Yao Peng, Cheng-Yuan Can J Gastroenterol Hepatol Research Article AIMS: Long-term risk stratification using combined liver stiffness (LS) and clinically relevant blood tests acquired at the baseline further beyond the sustained virologic response (SVR) visit for chronic hepatitis C (CHC) has not been thoroughly investigated. This study retrospectively investigated the prognostics of liver-related events (LREs) further beyond the SVR visit. METHODS: Cox regression and random forest models identified the key factors, including longitudinal LS and noninvasive test results, that could predict LREs, including hepatocellular carcinoma, during prespecified follow-ups from 2010 to 2021. Kaplan–Meier survival analysis estimated the significance of between-group risk stratification. RESULTS: Of the entire eligible cohort (n = 520) of CHC patients with SVR to antiviral therapy, 28 (5.4%) patients developed post-SVR LREs over a median follow-up period of 6.1 years (interquartile range = 3.5–8.7). The multivariate Cox regression analysis identified two significant predictors of LREs after the year 3 post-SVR (Y3PSVR) baseline (LRE, n = 15 of 28, 53.6%, median follow-up = 4.1 [1.6–6.4] years after Y3PSVR): LS at Y3PSVR (adjusted hazard ratio [aHR] = 3.980, 95% confidence interval [CI] = 2.085–7.597, P < 0.001), and α-fetoprotein (AFP) at Y3PSVR (aHR = 1.017, 95% CI = 1.001–1.034, P=0.034). LS ≥1.45 m/s and AFP ≥3.00 ng/mL for Y3PSVR yielded positive likelihood ratios of 4.24 and 2.62, respectively. Kaplan–Meier analysis revealed that among the stratified subgroups, the subgroup with concurrent LS ≥1.45 m/s and AFP ≥3.00 ng/mL at Y3PSVR exhibited the highest risk of LREs after Y3PSVR (log-rank P < 0.001). CONCLUSION: We recommend the combined use of concurrent LS and AFP in future prediction models for LREs in CHC. Patients with concurrently high LS and AFP values further beyond the SVR visit may require a recall policy involving intense surveillance. Hindawi 2022-07-04 /pmc/articles/PMC9273470/ /pubmed/35837486 http://dx.doi.org/10.1155/2022/5201443 Text en Copyright © 2022 Sheng-Hung Chen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Sheng-Hung
Lai, Hsueh-Chou
Su, Wen-Pang
Kao, Jung-Ta
Chuang, Po-Heng
Hsu, Wei-Fan
Wang, Hung-Wei
Hsieh, Tsung-Lin
Chen, Hung-Yao
Peng, Cheng-Yuan
Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C
title Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C
title_full Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C
title_fullStr Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C
title_full_unstemmed Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C
title_short Combined Liver Stiffness and Α-fetoprotein Further beyond the Sustained Virologic Response Visit as Predictors of Long-Term Liver-Related Events in Patients with Chronic Hepatitis C
title_sort combined liver stiffness and α-fetoprotein further beyond the sustained virologic response visit as predictors of long-term liver-related events in patients with chronic hepatitis c
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273470/
https://www.ncbi.nlm.nih.gov/pubmed/35837486
http://dx.doi.org/10.1155/2022/5201443
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