New classification of liver biopsy assessment for fibrosis in chronic hepatitis B patients before and after treatment

Yameng Sun(Capital Medical University), Jialing Zhou(Capital Medical University), Lin Wang(Capital Medical University), Xiaoning Wu(Capital Medical University), Yongpeng Chen(Nanfang Hospital), Hongxin Piao(Yanbian University Hospital), Lungen Lu(Shanghai Jiao Tong University), Wei Jiang(Sun Yat-sen University), Youqing Xu(Capital Medical University), Bo Feng(Peking University), Yuemin Nan(Hebei Medical University), Wen Xie(Capital Medical University), Guofeng Chen(302 Military Hospital of China), Huanwei Zheng(Fifth Hospital of Shijiazhuang), Hai Li(Logistics University of People's Armed Police Force), Huiguo Ding(Capital Medical University), Hui Liu(Capital Medical University), Fudong Lv(Capital Medical University), Chen Shao(China-Japan Friendship Hospital), Tailing Wang(China-Japan Friendship Hospital), Xiaojuan Ou(Capital Medical University), Bingqiong Wang(Capital Medical University), Shuyan Chen(Capital Medical University), Aileen Wee(National University of Singapore), Neil D. Theise(Mount Sinai Beth Israel), Hong You(Capital Medical University), Jidong Jia(Capital Medical University)
Hepatology
December 27, 2016
Cited by 156

Abstract

Liver fibrosis is the net result of dynamic changes between fibrogenesis and fibrolysis. Evidence has shown that antiviral therapy can reverse liver fibrosis or even early cirrhosis caused by hepatitis B virus. However, current evaluation systems mainly focus on the severity of, but not the dynamic changes in, fibrosis. Here, we propose a new classification to evaluate the dynamic changes in the quality of fibrosis, namely: predominantly progressive (thick/broad/loose/pale septa with inflammation); predominately regressive (delicate/thin/dense/splitting septa); and indeterminate, which displayed an overall balance between progressive and regressive scarring. Then, we used this classification to evaluate 71 paired liver biopsies of chronic hepatitis B patients before and after entecavir-based therapy for 78 weeks. Progressive, indeterminate, and regressive were observed in 58%, 29%, and 13% of patients before treatment versus in 11%, 11%, and 78% after treatment. Of the 55 patients who showed predominantly regressive changes on posttreatment liver biopsy, 29 cases (53%) had fibrosis improvement of at least one Ishak stage, and, more interestingly, 25 cases (45%) had significant improvement in terms of Laennec substage, collagen percentage area, and liver stiffness despite remaining in the same Ishak stage. CONCLUSION: This new classification highlights the importance of assessing and identifying the dynamic changes in the quality of fibrosis, especially relevant in the era of antiviral therapy.(Hepatology 2017;65:1438-1450).


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