Controlled Attenuation Parameter Is Associated with a Distinct Systemic Inflammatory Milieu after Clearance of HCV

Yanqin Du1,2, Tanvi Khera1,3,4, Zhaoli Liu5,6

  • 1Department of Gastroenterology and Hepatology, University Hospital Essen, University Duisburg-Essen, 45147 Essen, Germany.

Biomedicines
|June 28, 2023
PubMed

Insights

Persistent hepatic steatosis after Hepatitis C virus (HCV) clearance is linked to specific inflammatory mediators. Fibroblast growth factor 21 (FGF-21) and Interleukin-18 receptor 1 (IL-18R1) levels were elevated, while Stem Cell Factor (SCF) and TWEAK levels decreased post-HCV treatment.

Area of Science:

  • Hepatology
  • Virology
  • Immunology

Background:

  • Hepatitis C virus (HCV) infection is linked to lipid metabolism issues and hepatic steatosis.
  • Steatosis often persists even after successful HCV clearance, with unclear underlying mechanisms.

Purpose of the Study:

  • To investigate the association between 92 soluble inflammatory mediators (SIMs) and hepatic steatosis grade after HCV clearance.
  • To identify biomarkers predicting steatosis severity post-direct-acting antiviral agent (DAA) treatment.

Main Methods:

  • Analysis of 94 patients with chronic HCV who achieved sustained viral response (SVR) after DAA treatment.
  • Classification of patients into steatosis groups using controlled attenuation parameter (CAP) measurements.
  • Quantification of 92 SIMs and correlation with CAP values, ALT, γ-GT, and liver stiffness.

Main Results:

  • Four SIMs (SCF, TWEAK, FGF-21, IL-18R1) showed significant association with CAP values post-HCV clearance.
  • Elevated FGF-21 and IL-18R1 levels were observed in patients with higher CAP (> 299 dB/m).
  • Reduced SCF and TWEAK levels were noted in patients with higher CAP values.

Conclusions:

  • SCF, TWEAK, FGF-21, and IL-18R1 are potential biomarkers for steatosis status after HCV clearance.
  • These proteins may play a role in the pathogenesis of steatosis, potentially contributing to nonalcoholic steatohepatitis (NASH) post-SVR.
  • Further research is needed to elucidate the role of these biomarkers in post-SVR NASH development.