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Predictive value of serum S100A8/A9 for liver dysfunction in pregnant women with chronic hepatitis B
Weiwei Geng1, Hong Yu2, Yuan Li3
1Department of Obstetrics, Yancheng Maternity and Child Health Care Hospital, Yancheng Maternal and Child Health Hospital Affiliated to Yangzhou University School of Medicine, Yancheng, 224000, Jiangsu, China.
Background:
S100 calcium-binding protein A8/A9 (S100A8/A9) is a marker of innate immune activation and inflammation, but its value in predicting liver dysfunction in HBV-infected pregnant women remains unclear. This study aims to explore the predictive value of early-pregnancy serum S100A8/A9 for mid-to-late pregnancy liver dysfunction in chronic HBV-infected pregnant women, and its correlation with adverse pregnancy outcomes.
Methods:
A retrospective cohort study included 139 chronic HBV-infected pregnant women. Serum S100A8/A9 levels were measured via ELISA, and participants were subsequently divided into abnormal liver function (ALF) and normal liver function (NLF) groups based on mid-to-late pregnancy liver function. Logistic regression analysis identified independent risk factors for abnormal liver function and adverse pregnancy outcomes, while receiver operating characteristic curves evaluated S100A8/A9's predictive efficacy.
Results:
Early-pregnancy serum S100A8/A9 levels were significantly higher in the ALF group than in the NLF group, and positively correlated with HBV-DNA load and ALT. Elevated S100A8/A9 was an independent risk factor for liver dysfunction and predictor of adverse pregnancy outcomes. ROC curve analysis showed S100A8/A9 had an AUC of 0.882 for identifying liver dysfunction.
Conclusions:
Early-pregnancy serum S100A8/A9 may serve as a potential predictive marker for liver function impairment and adverse pregnancy outcomes in chronic HBV-infected women, helping with early clinical identification and management.
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