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      Quantitative assessment of liver fibrosis (qFibrosis) reveals precise outcomes in Ishak “stable” patients on anti-HBV therapy

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          Abstract

          Current widely used semiquantitative histological assessment methods are insensitive to identify subtle changes of liver fibrosis. Therefore, to precisely assess therapeutic efficacy on chronic hepatitis B (CHB), we explored the utility of qFibrosis (a fully-quantitative morphometric method employing second harmonic generation/two photon excitation fluorescence) in liver fibrosis evaluation. Fibrosis changes were evaluated by Ishak fibrosis scoring and qFibrosis in CHB patients with paired liver biopsies before and after 78 weeks’ antiviral therapy. A total of 162 patients with qualified paired biopsies were enrolled. Ishak fibrosis scoring revealed that 42.6% (69/162) of the patients achieved fibrosis regression (≥1-point decrease), 51.9% (84/162) remained stable, and 5.5% (9/162) showed progression (≥1-point increase). qFibrosis showed similar trends in the groups of regression and progression patients as evaluated by Ishak. However, in Ishak stable patients, qFibrosis revealed hitherto undetected changes, allowing for further subcategorization into regression ( “Regression by qFibrosis”; 40/84, 47.6%), stable (29/84, 34.5%), and progression (“ Progression by qFibrosis”; 15/84, 17.9%) groups. These newly fine-tuned categories were supported by changes of morphological parameters of fibrosis, collagen percentage area, and liver stiffness measurements. In conclusion, qFibrosis can be used to quantitatively identify subtle changes of liver fibrosis in CHB patients after antiviral therapy.

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          Histological grading and staging of chronic hepatitis.

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            Non-invasive evaluation of liver fibrosis using transient elastography.

            Transient elastography (TE, FibroScan) is a novel non-invasive method that has been proposed for the assessment of hepatic fibrosis in patients with chronic liver diseases, by measuring liver stiffness. TE is a rapid and user-friendly technique that can be easily performed at the bedside or in the outpatient clinic with immediate results and good reproducibility. Limitations include failure in around 5% of cases, mainly in obese patients. So far, TE has been mostly validated in chronic hepatitis C, with diagnostic performance equivalent to that of serum markers for the diagnosis of significant fibrosis. Combining TE with serum markers increases diagnostic accuracy and as a result, liver biopsy could be avoided for initial assessment in most patients with chronic hepatitis C. This strategy warrants further evaluation in other aetiological types of chronic liver diseases. TE appears to be an excellent tool for early detection of cirrhosis and may have prognostic value in this setting. As TE has excellent patient acceptance it could be useful for monitoring fibrosis progression and regression in the individual case, but more data are awaited for this application. Guidelines are needed for the use of TE in clinical practice.
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              Classification of chronic viral hepatitis: a need for reassessment.

              P Scheuer (1991)
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                Author and article information

                Contributors
                jia_jd@ccmu.edu.cn
                youhong30@sina.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                14 February 2018
                14 February 2018
                2018
                : 8
                : 2989
                Affiliations
                [1 ]ISNI 0000 0004 0369 153X, GRID grid.24696.3f, Liver Research Center, Beijing Key Laboratory of Translational Medicine in Liver Cirrhosis, National Clinical Research Center for Digestive Disease, Beijing Friendship Hospital, , Capital Medical University, ; Beijing, 100050 China
                [2 ]GRID grid.416466.7, Department of Infectious Diseases, , Nanfang Hospital, Southern Medical University, ; Guangzhou, 510515 China
                [3 ]ISNI 0000 0004 1758 0638, GRID grid.459480.4, Infectious Disease Department, , Affiliated Hospital of Yanbian University, ; Yanji, 133000 China
                [4 ]ISNI 0000 0004 0368 8293, GRID grid.16821.3c, Department of Gastroenterology and Hepatology, Shanghai General Hospital, , Shanghai Jiaotong University School of Medicine, ; Shanghai, 200080 China
                [5 ]ISNI 0000 0004 0369 153X, GRID grid.24696.3f, Department of Gastroenterology and Hepatology, Beijing Youan Hospital, , Capital Medical University, ; Beijing, 100069 China
                [6 ]GRID grid.452209.8, Department of Traditional and Western Medical Hepatology, , Third Hospital of Hebei Medical University, ; Shijiazhuang, 050051 China
                [7 ]ISNI 0000 0004 1755 3939, GRID grid.413087.9, Department of Gastroenterology, , Zhongshan Hospital, Fudan University, ; Shanghai, 200032 China
                [8 ]ISNI 0000 0004 1771 3349, GRID grid.415954.8, Pathology Department, , China-Japan Friendship Hospital, ; Beijing, 100029 China
                [9 ]ISNI 0000 0004 0369 153X, GRID grid.24696.3f, Pathology Department, Beijing Youan Hospital, , Capital Medical University, ; Beijing, 100069 China
                [10 ]Department of Pathology, Yong Loo Lin School of Medicine, National University of Singapore, National University Hospital, Singapore, 119074 Singapore
                [11 ]ISNI 0000 0004 1936 8753, GRID grid.137628.9, Department of Pathology, , New York University School of Medicine, ; New York, NY 10016 USA
                Author information
                http://orcid.org/0000-0002-9015-9861
                http://orcid.org/0000-0001-9409-1158
                Article
                21179
                10.1038/s41598-018-21179-2
                5813020
                29445243
                e0023e30-abeb-4575-acfa-54a6182fec5e
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 13 November 2017
                : 29 January 2018
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