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Author Spotlight: Advancing Hepatic Fibrosis Diagnosis Using Magnetic Resonance Elastography and AI
Published on: July 21, 2023
Elastography is unable to exclude cirrhosis after sustained virological response in HCV-infected patients with
Teresa Broquetas1,2, Paula Herruzo-Pino2, Zoe Mariño3
1Liver Section, Gastroenterology Department, Hospital del Mar, Barcelona, Spain.
Insights
Even after successful hepatitis C treatment, cirrhosis persists in over half of patients with advanced liver disease. Non-invasive tests like transient elastography show poor accuracy for detecting cirrhosis post-treatment, necessitating long-term patient monitoring.
Area of Science:
- Hepatology
- Virology
- Diagnostic Imaging
Background:
- The correlation between liver fibrosis staging via transient elastography (TE) and outcomes in hepatitis C virus (HCV)-infected patients with compensated advanced chronic liver disease (cACLD) following sustained virological response (SVR) remains unclear.
- Understanding this relationship is crucial for managing patients post-HCV eradication.
Purpose of the Study:
- To assess the accuracy of transient elastography (TE) in identifying cirrhosis in patients with compensated advanced chronic liver disease (cACLD) three years after achieving a sustained virological response (SVR) to hepatitis C virus (HCV) treatment.
Main Methods:
- A prospective, multi-centric study enrolled HCV-cACLD patients prior to direct-acting antiviral (DAA) therapy.
- The diagnostic accuracy of TE to identify cirrhosis (METAVIR F4) three years post-SVR was evaluated using the area under the receiver operating characteristic curve (AUROC).
- Liver biopsy, TE, APRI, and FIB-4 scores were assessed before and after treatment.
Main Results:
- Among 746 patients, 76 underwent liver biopsy 3 years post-SVR, revealing cirrhosis in 41 (53.9%).
- TE values, APRI, and FIB-4 scores improved post-SVR, but TE accuracy for cirrhosis detection was poor (AUROC=0.75).
- HCV genotype 3 and pre-treatment TE were significant predictors of cirrhosis post-SVR, while post-SVR TE, APRI, and FIB-4 showed limited diagnostic value.
Conclusions:
- Cirrhosis is prevalent in over half of HCV-cACLD patients three years after SVR, despite improvements in liver function and non-invasive test scores.
- The low diagnostic accuracy of non-invasive methods, including TE, APRI, and FIB-4, after SVR highlights the need for continued long-term surveillance in these patients.
- HCV genotype 3 and baseline TE are crucial factors for predicting long-term fibrosis progression.
Background:
Liver fibrosis and transient elastography (TE) correlation in hepatitis C virus (HCV)-infected patients with compensated advanced chronic liver disease (cACLD) after the sustained virological response (SVR) is unknown.
Aims:
To evaluate TE accuracy at identifying cirrhosis 3 years after HCV-eradication.
Methods:
Prospective, multi-centric study including HCV-cACLD patients before direct-acting antivirals (DAA). Diagnostic accuracy of TE (area under ROC, AUROC) to identify cirrhosis 3 years after SVR was evaluated.
Results:
Among 746 HCV-infected patients (95.4% with TE ≥10 kPa), 76 (10.2%) underwent a liver biopsy 3 years after SVR. Before treatment, 46 (63%) showed a TE>15 kPa. The TE before DAA was the best variable for predicting cirrhosis (METAVIR, F4) after SVR (AUROC = 0.79). Liver function parameters, serological non-invasive tests (APRI and FIB-4), and TE values improved after SVR. However, liver biopsy 3 years after HCV elimination (median time = 38.4 months) showed cirrhosis in 41 (53.9%). Multivariate analysis (OR (95% CI), P) showed that HCV-genotype 3 (20.81 (2.12-201.47), .009), and TE before treatment (1.21 (1.09-1.34), <.001) were the only variables associated with cirrhosis after SVR. However, the accuracy of TE after SVR was poor (AUROC = 0.75) and 6 (27.3%) out of 22 patients with a TE <8 kPa had cirrhosis. Similar results were found with APRI and FIB-4 scores.
Conclusions:
Cirrhosis is present, 3 years after SVR, in more than half of HCV-cACLD patients even with the normalisation of liver function parameters, serological non-invasive tests and TE values. The low diagnostic accuracy of non-invasive methods after SVR reinforces the need for long-term surveillance.
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