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Published on: November 27, 2019
Lipocalin-2 serum levels are increased in acute hepatic failure
G A Roth1, S Nickl, D Lebherz-Eichinger
1Department of Anesthesiology, General Intensive Care and Pain Medicine, Medical University of Vienna, Vienna, Austria. georg.roth@meduniwien.ac.at
Insights
Serum Lipocalin-2 (LCN-2) levels are elevated in patients with acute liver failure (ALF) and acute-on-chronic liver failure (ACLF) compared to chronic hepatic failure (CHF). LCN-2 may help differentiate acute from chronic liver disease.
Area of Science:
- Biochemistry
- Hepatology
- Immunology
Background:
- Lipocalin-2 (LCN-2) is a protein upregulated during inflammation and infection.
- Elevated LCN-2 serum levels are associated with cellular stress.
Purpose of the Study:
- To investigate the role of LCN-2 in acute hepatic failure (AHF).
- To assess LCN-2 relevance in patients treated with the molecular adsorbent recirculating system (MARS).
Main Methods:
- Serum LCN-2 concentrations were measured using ELISA.
- Patients included 8 with ACLF/ALF treated with MARS and 14 with CHF.
- LCN-2 levels were assessed before and after the first MARS session.
Main Results:
- Baseline LCN-2 serum concentrations were significantly higher in ACLF and ALF patients compared to CHF patients (P = .004 and P = .0086).
- No significant difference in LCN-2 levels was observed between ALF and ACLF groups.
- Serum LCN-2 levels remained unchanged during MARS treatment.
Conclusions:
- Elevated serum LCN-2 may distinguish acute from chronic hepatic failure.
- LCN-2 could serve as a biomarker for monitoring disease severity and progression in liver failure.
Abstract:
Lipocalin-2 (LCN-2), which is expressed in immunocytes as well as hepatocytes, is upregulated in cells under stress from infection or inflammation with increase in serum levels. We sought to investigate the relevance of LCN-2 in the setting of acute hepatic failure, particularly when addressed with the molecular adsorbent recirculating system (MARS). We measured serum LCN-2 concentrations with enzyme-linked immunosorbent assay (ELISA) in 8 patients with acute-on-chronic-liver failure (ACLF) and acute liver failure (ALF) who were treated with MARS. The controls were 14 patients with stable chronic hepatic failure (CHF). LCN-2 was determined immediately before and after the first MARS session. Baseline LCN-2 serum concentrations were significantly increased among ACLF and ALF patients as compared with CHF (P = .004 and P = .0086, respectively). There was no significant difference between the ALF and ACLF group. Moreover, serum LCN-2 levels did not change significantly during the MARS treatment. Serum LCN-2 levels, therefore, may be useful to discern acute from chronic hepatic failure and to monitor the course as well as the severity of the disease.
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