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Visualization and Analysis of Blood Flow and Oxygen Consumption in Hepatic Microcirculation: Application to an Acute Hepatitis Model
Published on: August 4, 2012
Correlation of effective hepatic blood flow with liver pathology in patients with hepatitis B virus
Xin Shu1, Haixia Sun1, Xiaoan Yang1
1Department of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Insights
Effective hepatic blood flow (EHBF) decreases with liver disease progression. This study found EHBF correlates with liver pathology, showing potential for predicting inflammation and fibrosis in hepatitis B virus patients.
Area of Science:
- Hepatology
- Medical Diagnostics
- Biomedical Engineering
Background:
- Effective hepatic blood flow (EHBF) is a key indicator of liver health.
- Progression of liver disease is associated with a decline in EHBF.
- Accurate assessment of liver pathology is crucial for patient management.
Purpose of the Study:
- To investigate the correlation between EHBF and liver pathology in patients with hepatitis B virus (HBV).
- To explore the potential of EHBF measurements for predicting the degree of liver inflammation and fibrosis.
Main Methods:
- Enrolled 207 HBV patients undergoing liver biopsy and indocyanine green (ICG) clearance tests.
- Measured EHBF using ICG clearance and assessed liver histology via Scheuer scoring.
- Collected demographic, biochemical, and FibroScan data for statistical analysis.
Main Results:
- EHBF levels significantly decreased with increasing stages of liver inflammation and fibrosis (P < 0.01).
- EHBF showed significant negative associations with liver enzymes and stiffness measurements (P < 0.05).
- EHBF effectively differentiated patients with and without liver inflammation/fibrosis, with high diagnostic accuracy (AUROC up to 0.827 for inflammation).
Conclusions:
- EHBF levels are significantly correlated with liver pathology in HBV patients.
- EHBF serves as a reliable indicator of liver inflammation and fibrosis.
- EHBF is particularly effective in identifying early-stage liver disease, especially in patients without overt inflammation or fibrosis.
Background And Aims:
Effective hepatic blood flow (EHBF) decreases with liver disease progression, and identifying liver pathology is critical for patients with liver disease. This study was designed to elucidate the correlation between EHBF and liver pathology and explore the potential of EHBF for predicting the degree of liver pathology.
Methods:
In this study, 207 patients with hepatitis B virus (HBV) who underwent liver biopsy and indocyanine green (ICG) clearance tests were enrolled. EHBF was measured using the ICG clearance test, and liver tissue was histologically analyzed to determine the pathological stage according to the Scheuer scoring system. Demographic data, biochemical indexes, and FibroScan data were collected for statistical analysis.
Results:
EHBF levels decreased as the liver histological stages of inflammation and fibrosis increased (P < 0.01). EHBF was significantly negatively associated with the levels of alanine aminotransferase, aspartate aminotransferase, gamma-glutamyl transpeptidase, alkaline phosphatase, aspartate aminotransferase-to-platelet ratio index, fibrosis index based on the four factors, and liver stiffness measurement (P < 0.05). The EHBF levels of patients without liver inflammation (G0) were significantly higher than those of patients with liver inflammation (G1-4) (P < 0.001). The area under the receiver operating characteristic curve (AUROC) value for discriminating patients without liver inflammation was 0.827, and the optimal cutoff value was 0.936 L/min. The EHBF levels of patients with severe liver inflammation (G4) were significantly lower than those of patients with G0-3 liver inflammation (P < 0.001). The AUROC value for discriminating patients with severe liver inflammation was 0.792, and the optimal cutoff value was 0.552 L/min. The EHBF levels of patients without liver fibrosis (S0) were significantly higher than those of patients with liver fibrosis (S1-4) (P < 0.001). The AUROC value for discriminating patients without liver fibrosis was 0.633, and the optimal cutoff value was 1.173 L/min. The EHBF levels of patients with liver cirrhosis (S4) were significantly lower than those of patients with S0-3 liver fibrosis (P < 0.001). The AUROC value for discriminating patients with liver cirrhosis (S4) was 0.630, and the optimal cutoff value was 0.562 L/min.
Conclusions:
EHBF levels and liver pathology are significantly correlated. EHBF could effectively reflect liver inflammation and fibrosis in patients infected with HBV, especially for patients without liver inflammation or liver fibrosis.
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