Viral clearance ameliorates hematological and inflammatory markers among diabetic patients infected with hepatitis C genotype 4

Clin Exp Med. 2020 May;20(2):231-240. doi: 10.1007/s10238-019-00605-3. Epub 2020 Feb 19.

Abstract

The achievement of virological response in the treatment of hepatitis C virus (HCV) can improve the extrahepatic manifestations. The present study aimed to investigate the effect of HCV eradication after sofosbuvir/daclatasvir (SOF/DCV) therapy on hematological and inflammatory biomarkers in type 2 diabetic patients infected with HCV genotype 4. Between October 2017 and August 2018, among 145 patients with HCV genotype 4, 30 patients were enrolled in the study based on the fact that they have type 2 diabetes. Enrolled HCV-diabetic patients were treated for 12 weeks with SOF/DCV regimen. Patients were screened by laboratory investigations before treatment (baseline values) and after HCV treatment (post-treatment values). Additionally, 30 healthy individuals were enrolled as a control group. Among the patient's cohort, the sustained virological response was achieved by 100% of the treated patients after 12 weeks of SOF/DCV therapy. Moreover, the levels of insulin resistance (HOMA-IR), nitric oxide, interleukin-1β, red cell distribution width, platelet distribution width, mean platelet volume were improved significantly (P < 0.001) in treated patients after successful viral clearance compared to baseline values. In addition, virological clearance exhibited positive correlations with interleukin-1β, nitric oxide, leukocytes count, red cell distribution width, and mean platelet volume. In conclusion, the data suggest the potential amelioration effect of HCV eradication after treatment with SOF/DCV regimen on the inflammatory status among HCV-diabetic patients which is reflected by the noticeable improvement of altered hematological indices and inflammatory biomarkers.

Keywords: DAA-based regimen; HCV genotype 4; Hematological profile; Inflammatory biomarkers; Type 2 diabetes mellitus.

Publication types

  • Controlled Clinical Trial
  • Multicenter Study

MeSH terms

  • Adult
  • Antiviral Agents / therapeutic use*
  • Biomarkers / blood
  • Carbamates / therapeutic use
  • Diabetes Mellitus, Type 2 / blood*
  • Diabetes Mellitus, Type 2 / virology
  • Female
  • Genotype
  • Glycated Hemoglobin / analysis
  • Hepacivirus / drug effects
  • Hepacivirus / genetics*
  • Hepatitis C / drug therapy*
  • Hepatitis C / virology
  • Humans
  • Imidazoles / therapeutic use
  • Inflammation / drug therapy
  • Inflammation / virology
  • Insulin Resistance
  • Interleukin-1beta / blood
  • Male
  • Middle Aged
  • Pyrrolidines / therapeutic use
  • Sofosbuvir / therapeutic use
  • Sustained Virologic Response
  • Treatment Outcome
  • Valine / analogs & derivatives
  • Valine / therapeutic use

Substances

  • Antiviral Agents
  • Biomarkers
  • Carbamates
  • Glycated Hemoglobin A
  • IL1B protein, human
  • Imidazoles
  • Interleukin-1beta
  • Pyrrolidines
  • hemoglobin A1c protein, human
  • Valine
  • daclatasvir
  • Sofosbuvir