Turkish Journal of Gastroenterology
Liver - Original Article

The Relationship Between Collagen Proportionate Area and Hepatitis B Surface Antigen Levels in E Antigen Positive Hepatitis B Cirrhosis

1.

Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

2.

Department of Gastroenterology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

Turk J Gastroenterol 2022; 33: 62-67
DOI: 10.5152/tjg.2022.20796
Read: 361 Downloads: 30 Published: 10 January 2022

Background: Quantitative serum hepatitis B surface antigen (HbsAg) has been widely used as a biomarker for treatment response and prognosis in chronic hepatitis B infection, and has recently been found associated with liver histology in e-antigen positive patients. A histological measurement as a continuous variable—collagen proportionate area (CPA)—is appropriate to assess liver fibrosis degree and substages cirrhosis. We, therefore, aimed to explore the association between serum quantitative HBsAg and CPA in e antigenpositive hepatitis B cirrhosis.

Methods: Liver fibrosis staging was evaluated by METAVIR semiquantitative scoring system, only patients with METAVIR fibrosis stage 4 were included. All liver sections were stained with picroSirius red for determination of collagen quantification by digital image analysis.

Results: Mean CPA value was 23.46%. The percentage of patients with different classification of CPA (30%) were 25.8%, 57.8%, and 16.4%, respectively. A modest correlation was found between CPA and serum HBsAg level (r = –0.306, P =.001). Hepatitis B surface antigen level is independently associated with CPA in multivariable linear regression analyses.

Conclusion: Serum HBsAg levels can predict liver fibrosis determined by CPA in HBeAg-positive hepatitis B cirrhosis.

Cite this article as: Shi Q, Yu R, Sun Q, Wang C, Yao J, Zhang L. The relationship between collagen proportionate area and hepatitis B surface antigen levels in E antigen positive hepatitis B cirrhosis. Turk J Gastroenterol. 2022; 33(1): 62-67.

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