Hepatitis C infection and clearance: impact on atherosclerosis and cardiometabolic risk factors

Aya Mostafa1, Mostafa K Mohamed, Mohamed Saeed

  • 1Department of Community Medicine, Faculty of Medicine, AinShams University, Cairo, Egypt.

Gut
|June 30, 2010
PubMed

Insights

Hepatitis C virus (HCV) infection is linked to diabetes and favorable lipids, but atherosclerosis risk remains similar after HCV clearance. Chronic HCV infection directly increases atherosclerosis risk, even after accounting for other cardiovascular factors.

Area of Science:

  • Hepatology and Viral Infections
  • Cardiovascular Disease Research
  • Metabolic Syndrome Studies

Background:

  • Chronic hepatitis C (HCV) infection is paradoxically associated with diabetes and favorable lipid profiles.
  • This association presents a complex cardiometabolic profile in individuals with HCV.

Purpose of the Study:

  • To investigate the impact of HCV infection and its clearance on atherosclerosis.
  • To examine the cardiometabolic response following HCV eradication.

Main Methods:

  • A cross-sectional study conducted in Egypt.
  • Involved 329 chronically infected, 173 cleared infection, and 795 never infected participants (age ≥35).
  • Assessed diabetes, glucose, lipids, visceral fat, and carotid intima-media thickness (IMT) via ultrasound.

Main Results:

  • Increased diabetes prevalence and mesenteric fat deposition in both chronic and cleared HCV groups compared to never infected.
  • Lower LDL cholesterol in chronic HCV, normalizing after clearance.
  • No significant difference in carotid IMT by infection status initially, but increased IMT in chronic HCV after adjusting for risk factors.

Conclusions:

  • HCV clearance normalizes lipid profiles but does not fully resolve hyperglycemia or visceral adiposity.
  • Chronic HCV infection appears to have a direct detrimental effect on atherosclerosis (increased IMT).
  • Cardiovascular risk in HCV is multifactorial, influenced by infection status, metabolic changes, and clearance outcomes.
Abstract

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