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Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage

BACKGROUND: Patients with chronic hepatitis B (CHB) concomitant with nonalcoholic fatty liver disease (NAFLD) are increasing. OBJECTIVES: To identify pathological features that can be used to differentiate between chronic inflammation caused by CHB and that caused by NAFLD. METHODS: Patients with CH...

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Autores principales: Zhu, Yong-fen, Wang, Jin, Fang, Jia-zhui, Yang, Qiao, Lv, Fang-fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189318/
https://www.ncbi.nlm.nih.gov/pubmed/32382264
http://dx.doi.org/10.1155/2020/3584568
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author Zhu, Yong-fen
Wang, Jin
Fang, Jia-zhui
Yang, Qiao
Lv, Fang-fang
author_facet Zhu, Yong-fen
Wang, Jin
Fang, Jia-zhui
Yang, Qiao
Lv, Fang-fang
author_sort Zhu, Yong-fen
collection PubMed
description BACKGROUND: Patients with chronic hepatitis B (CHB) concomitant with nonalcoholic fatty liver disease (NAFLD) are increasing. OBJECTIVES: To identify pathological features that can be used to differentiate between chronic inflammation caused by CHB and that caused by NAFLD. METHODS: Patients with CHB (n = 31) needing antiviral treatment, NAFLD (n = 50), or CHB-NAFLD (n = 51) who underwent biopsy were retrospectively enrolled. Pathological characteristics of chronic inflammation were evaluated using the METAVIR scoring system. The rates of three pathological characteristics were first compared in patients with NAFLD and those with CHB, then compared after fibrosis matching, and were finally compared in CHB-NAFLD patients with different viral loads. RESULTS: The rates of interface hepatitis over grade 2 and fibrosis over grade 2 were significantly higher in the CHB group than in the NAFLD group (100% vs. 4% and 80.6% vs. 22%; both P < 0.0001), while no significant difference was observed in the rate of lobular inflammation over grade 2 between the two groups. After fibrosis matching, in patients with F0–2 fibrosis, the rate of interface hepatitis over grade 2 in CHB was significantly higher than that in NAFLD (100% vs. 0%; P < 0.0001). In CHB-NAFLD patients with F0–2 fibrosis, the rate of interface hepatitis over grade 2 in cases with a high viral load was significantly higher than cases with a low viral load (66.6% vs. 0%; P < 0.0001). The rate of lobular inflammation showed no difference between groups. CONCLUSION: Interface hepatitis over grade 2 can be used for the differential diagnosis of chronic inflammation associated with CHB or NAFLD in the early stage.
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spelling pubmed-71893182020-05-07 Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage Zhu, Yong-fen Wang, Jin Fang, Jia-zhui Yang, Qiao Lv, Fang-fang Gastroenterol Res Pract Research Article BACKGROUND: Patients with chronic hepatitis B (CHB) concomitant with nonalcoholic fatty liver disease (NAFLD) are increasing. OBJECTIVES: To identify pathological features that can be used to differentiate between chronic inflammation caused by CHB and that caused by NAFLD. METHODS: Patients with CHB (n = 31) needing antiviral treatment, NAFLD (n = 50), or CHB-NAFLD (n = 51) who underwent biopsy were retrospectively enrolled. Pathological characteristics of chronic inflammation were evaluated using the METAVIR scoring system. The rates of three pathological characteristics were first compared in patients with NAFLD and those with CHB, then compared after fibrosis matching, and were finally compared in CHB-NAFLD patients with different viral loads. RESULTS: The rates of interface hepatitis over grade 2 and fibrosis over grade 2 were significantly higher in the CHB group than in the NAFLD group (100% vs. 4% and 80.6% vs. 22%; both P < 0.0001), while no significant difference was observed in the rate of lobular inflammation over grade 2 between the two groups. After fibrosis matching, in patients with F0–2 fibrosis, the rate of interface hepatitis over grade 2 in CHB was significantly higher than that in NAFLD (100% vs. 0%; P < 0.0001). In CHB-NAFLD patients with F0–2 fibrosis, the rate of interface hepatitis over grade 2 in cases with a high viral load was significantly higher than cases with a low viral load (66.6% vs. 0%; P < 0.0001). The rate of lobular inflammation showed no difference between groups. CONCLUSION: Interface hepatitis over grade 2 can be used for the differential diagnosis of chronic inflammation associated with CHB or NAFLD in the early stage. Hindawi 2020-04-20 /pmc/articles/PMC7189318/ /pubmed/32382264 http://dx.doi.org/10.1155/2020/3584568 Text en Copyright © 2020 Yong-fen Zhu et al. http://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
Zhu, Yong-fen
Wang, Jin
Fang, Jia-zhui
Yang, Qiao
Lv, Fang-fang
Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage
title Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage
title_full Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage
title_fullStr Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage
title_full_unstemmed Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage
title_short Interface Hepatitis over Grade 2 May Differentiate Chronic Inflammation Associated with CHB from NAFLD in the Early Stage
title_sort interface hepatitis over grade 2 may differentiate chronic inflammation associated with chb from nafld in the early stage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189318/
https://www.ncbi.nlm.nih.gov/pubmed/32382264
http://dx.doi.org/10.1155/2020/3584568
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