Improvement of glucose and lipid metabolism with pegylated interferon-a plus ribavirin therapy in Chinese patients chronically infected with genotype 1b hepatitis C virus

Ann Saudi Med. 2015 Jul-Aug;35(4):293-7. doi: 10.5144/0256-4947.2015.293.

Abstract

Background: Many epidemiological studies have demonstrated a significant association between Type 2 diabetes mellitus and abnormal lipid profiles with chronic HCV genotype 1 (GT1) infection. We examined the impact on glucose and lipid profiles of treating Chinese patients using pegylated interferon (Peg-IFN)-a and ribavirin (RBV).

Methods: We conducted a hospital-based clinical study of Chinese patients chronically infected with GT1b HCV. All the patients were treated for 48 weeks (PR48) with Peg-IFN-a (180 micro g once per week) or Peg-IFN-a (1.5 micro g/kg once per week) plus RBV (15 mg/kg per day). Fasting blood glucose (FBG), postprandial blood glucose (PBG-2h), glycosylated hemoglobin (HbA1c), total cholesterol (TC) and triglyceride (TG) levels, were measured at baseline, during therapy, at the end of therapy and at follow-up. In addition, liver stiffness (LS) by transient elastography, HCV RNA and ALT levels were also measured.

Results: We enrolled 116 patients. At the end of treatment (EOT) (week 48), HCV RNA was negative in all patients, 77.6% (90/116) of patients achieved sustained virologic response (SVR) 24 weeks after EOT, and 22.4% (26/116) did not achieve SVR. All parameters associated with liver inflammation, liver fibrosis, glucose and lipid metabolism had decreased significantly compared with baseline (P < .05) in SVR patients. However, there were no obvious changes in lipid metabolism in non-SVR patients.

Conclusion: PR48 therapy is still the primary treatment for Chinese patients with GT1b HCV infection and will remain so until oral anti-HCV agents are approved. It is beneficial in amelioration of liver histological status and glucose metabolism regardless of post-treatment virologic response.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alanine Transaminase / blood
  • Antiviral Agents / administration & dosage*
  • Blood Glucose / drug effects*
  • Blood Glucose / metabolism
  • China
  • Cholesterol / metabolism
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / virology
  • Drug Therapy, Combination
  • Elasticity Imaging Techniques
  • Fasting / blood
  • Female
  • Genotype
  • Glycated Hemoglobin / drug effects
  • Hepacivirus / drug effects
  • Hepacivirus / genetics*
  • Hepatitis C, Chronic / blood
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / virology
  • Humans
  • Interferon-alpha / administration & dosage*
  • Lipid Metabolism / drug effects*
  • Liver / diagnostic imaging
  • Liver / drug effects
  • Liver / virology
  • Male
  • Middle Aged
  • Postprandial Period
  • RNA, Viral / blood
  • Ribavirin / administration & dosage*
  • Triglycerides / metabolism

Substances

  • Antiviral Agents
  • Blood Glucose
  • Glycated Hemoglobin A
  • Interferon-alpha
  • RNA, Viral
  • Triglycerides
  • hemoglobin A1c protein, human
  • Ribavirin
  • Cholesterol
  • Alanine Transaminase