Abstract | BACKGROUND: AIM: METHODS: This cohort study analysed the prospective database of 290 CHC patients without a history of HCC who achieved HCV elimination by direct-acting antivirals. We calculated the FibroScan- aspartate aminotransferase (FAST) score 12 weeks after the end of treatment (pw12). The risk of HCC was analysed using the multivariable Cox proportional hazard model. RESULTS: HCV genotype (GT)1 was most prevalent at 72.4%, followed by GT2 (26.6%). Median follow-up period was 4.2 years (IQR 3.1-4.5). The cumulative HCC incidence for a FAST score ≥ 0.35 was significantly higher than that for a FAST score < 0.35 (log-rank test: P < 0.001). The annual HCC incidence rate for a FAST score ≥ 0.35 was significantly higher than that for a FAST score < 0.35, in patients with liver stiffness measurement (LSM) ≥10 kPa (adjusted hazard ratio [HR] 4.41, 95% confidence interval [CI] 1.30-15.0, P = 0.018). After adjusting for variables, including age, albumin, alpha-fetoprotein, the patatin-like phospholipase domain-containing the 3 (PNPLA3) rs738409 genotype, and pw12 fibrosis markers with FIB-4, non-alcoholic fatty liver disease fibrosis score, and LSM, FAST score ≥ 0.35 was associated with the development of HCC (adjusted HR 4.42, 95% CI 1.02-19.9, P = 0.043). CONCLUSIONS:
Steatohepatitis-related biomarkers with the FAST score are helpful for predicting the development of HCC after HCV elimination.
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Authors | Eiichi Ogawa, Koji Takayama, Satoshi Hiramine, Takeo Hayashi, Kazuhiro Toyoda |
Journal | Alimentary pharmacology & therapeutics
(Aliment Pharmacol Ther)
Vol. 52
Issue 5
Pg. 866-876
(09 2020)
ISSN: 1365-2036 [Electronic] England |
PMID | 32697871
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2020 John Wiley & Sons Ltd. |
Chemical References |
- AFP protein, human
- Antiviral Agents
- Biomarkers, Tumor
- alpha-Fetoproteins
|
Topics |
- Adult
- Aged
- Antiviral Agents
(therapeutic use)
- Biomarkers, Tumor
(analysis, blood, genetics)
- Carcinoma, Hepatocellular
(diagnosis, genetics, pathology)
- Cell Transformation, Viral
- Cohort Studies
- Disease Progression
- Fatty Liver
(blood, diagnosis, genetics)
- Female
- Genotype
- Hepacivirus
(drug effects, genetics, physiology)
- Hepatitis C, Chronic
(blood, complications, diagnosis, drug therapy)
- Humans
- Liver Neoplasms
(diagnosis, genetics, pathology)
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
- Prognosis
- Remission Induction
- Retrospective Studies
- alpha-Fetoproteins
(genetics)
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