Association of α-fetoprotein levels with liver stiffness measurement in outpatients with chronic hepatitis B

Author:

Wang Juan1,Zhang Pengpeng2,Liao Juan1,Zhu Yan3,Liu Xiaoli4,Tang Hong1ORCID

Affiliation:

1. Center of Infectious Diseases, West China Hospital of Sichuan University, Chengdu, China

2. Transplantation Center, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China

3. Employee Healthcare Department, West China Hospital of Sichuan University, Chengdu, China

4. Department of Infectious Diseases, Hunan Provincial Corps Hospital, Chinese People’s Armed Police Forces, Hunan, China

Abstract

Abstract The association between α-fetoprotein (AFP) levels with the assessment of liver stiffness (LS) in chronic hepatitis B (CHB) patients were explored. A total of 283 outpatients with CHB were enrolled. Patient age, alanine aminotransferase (ALT), aspartate aminotransferase (AST), AFP, platelet (PLT), total bilirubin (TB), direct bilirubin (DB), alkaline phosphatase (ALP), albumin (ALB), globulin, and albumin/globulin (A/G) levels were associated with LS values in the univariate model (P<0.05). Significant associations between AFP and PLT levels with LS values were observed when both variables were included in the multivariate analysis models. Receiver operation characteristic (ROC) analysis indicated that the combination of AFP and PLT levels could enhance the predictive performance of liver fibrosis (area under the curve (AUC) = 0.819, P<0.001) and that PLT levels (PLT < 100 × 109/l) combined with high AFP levels (AFP > 8 ng/ml) significantly increased the prediction of liver fibrosis (OR = 11.216). More importantly, LS values associated with higher AFP levels (AFP > 8 ng/ml), independently of higher ALT or AST values, were significantly higher than those of low AFP level groups. In conclusion, in Chinese outpatients with CHB, AFP outperformed ALT and/or AST levels in terms of their association with LS. AFP and PLT levels were independently associated with LS, and their combined assessment could enhance the diagnostic and predictive performance of liver fibrosis among CHB patients.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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