Sustained virological response and metabolic risk factors are associated with mortality in patients with chronic hepatitis C

PLoS One. 2019 Jan 9;14(1):e0208858. doi: 10.1371/journal.pone.0208858. eCollection 2019.

Abstract

Background and aim: Previous studies have reported that sustained virological response (SVR) to interferon-based treatment reduces the risk of mortality in chronic hepatitis C (CHC) patients, mainly in cirrhotic patients. A population-based study reported that metabolic risk factors increase the risk of mortality in CHC patients. We aim to investigate the association between SVR, metabolic risk factors and mortality in CHC patients with and without advanced fibrosis.

Methods: We collected data from 1452 CHC patients who underwent interferon-based therapy. All patients underwent liver biopsy prior to therapy. Mild fibrosis was defined as a modified Knodell score of 0-2, while advanced fibrosis was defined as a score of 3-4.

Results: 1452 patients were followed up for a median (IQR) of 6.6 (4.2-9.4) years, 1124 patients (77.4%) achieved SVR, 619 patients (42.6%) were advanced fibrosis. 14 patients with mild fibrosis and 55 patients with advanced fibrosis died during follow-up period. According to multivariate Cox regression analyses, SVR reduced the risks of all-cause mortality (HR, 0.21; 95% CI, 0.12-0.37; P<0.001), liver-related mortality (HR, 0.19; 95% CI, 0.10-0.38; P < .001), and non-liver-related mortality (HR, 0.26; 95% CI, 0.10-0.71; P = 0.009) in the patients with advanced fibrosis. SVR also reduced the risk of liver-related mortality (HR, 0.09; 95% CI, 0.01-0.60; P = 0.013) in the patients with mild fibrosis. Anti-hypertensive treatment increased the risks of all-cause mortality (HR, 6.1; 95% CI: 1.66-22.54; P = 0.006) and liver-related mortality (HR, 12.3; 95% CI: 1.4-108.5; P = 0.02) in the patients with mild fibrosis.

Conclusion: SVR and metabolic risk factors are associated with mortality in CHC patients given interferon-based treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use
  • Female
  • Hepatitis C, Chronic / drug therapy
  • Hepatitis C, Chronic / mortality*
  • Humans
  • Interferon-alpha / therapeutic use
  • Liver Cirrhosis / drug therapy
  • Liver Cirrhosis / mortality
  • Male
  • Middle Aged
  • Ribavirin / therapeutic use
  • Risk Factors
  • Sustained Virologic Response*

Substances

  • Antiviral Agents
  • Interferon-alpha
  • Ribavirin

Grants and funding

This study was supported by Grant CMRPG8G1181 from the Chang Gung Memorial Hospital-Kaohsiung Medical Center, Taiwan. The grant recipient is Dr. Yi-Hao Yen. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.