Lipids, glucose and iron metabolic alterations in chronic hepatitis C after viral eradication - comparison of the new direct-acting antiviral agents with the old regimens

Scand J Gastroenterol. 2018 Jun-Jul;53(7):857-863. doi: 10.1080/00365521.2018.1473486. Epub 2018 May 20.

Abstract

Background: Hepatitis C virus (HCV) is a unique virus which interacts with cholesterol, iron and insulin metabolism. There is limited data on the effects of direct-acting antiviral agents (DAAs) on metabolic profiles. We aimed at evaluating the behavior of metabolic risk factors of chronically HCV-infected patients after sustained virologic response (SVR), comparing the outcomes with the new DAAs versus the old treatment regimen Peg-interferon ± ribavirin.

Methods: A total of 178 patients who achieved SVR and completed one year of follow-up were prospectively included in this study: group 1 with 105 patients treated with DAAs and group 2 with 73 patients treated with old regimens. Outcomes included lipid, glucose and iron metabolism variation after SVR.

Results: There was a significant increase in total cholesterol in both groups (group 1: p < .001, 95% CI: 0.41-0.78; group 2: p < .001, 95% CI: 0.24-0.69). Triglyceride levels significantly decreased (p = .015, 95% CI: -0.33-0.04) in group 1 and increased (p = .014, 95% CI: 0.07-0.59) in group 2. LDL levels increased in group 1 (p = .029, 95% CI: 0.05-0.88), but no significant variation was found in group 2. No significant variation in HDL, fast glucose and iron was seen in both groups. There was a significant increase of HOMA (p = .002, 95% CI: 0.17592-0.72317) only in group 2. Ferritin serum levels significantly decreased (p < .001, 95% CI:-138.3-74.4) in group 1 but no significant variation was found in group 2.

Conclusion: Patients who have achieved SVR may have increased risk of cardiovascular outcomes due to development of hyperlipidemia and insulin resistance.

Keywords: Hepatitis C virus; direct-acting antiviral agents; glucose; iron; lipids; metabolism.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use*
  • Blood Glucose / analysis*
  • Cardiovascular Diseases / etiology
  • Drug Administration Schedule
  • Drug Therapy, Combination
  • Female
  • Ferritins / blood
  • Ferritins / metabolism*
  • Hepacivirus / drug effects
  • Hepatitis C, Chronic / blood
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / metabolism
  • Humans
  • Hyperlipidemias / etiology
  • Insulin Resistance
  • Lipid Metabolism / drug effects*
  • Lipids / blood
  • Logistic Models
  • Male
  • Middle Aged
  • Portugal
  • Sustained Virologic Response

Substances

  • Antiviral Agents
  • Blood Glucose
  • Lipids
  • Ferritins