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Interferon-based therapy reduces risk of stroke in chronic hepatitis C patients: a population-based cohort study in
1Division of Gastroenterology, Department of Internal Medicine, Buddhist Tzu Chi General Hospital, Taipei Branch, Taipei, Taiwan.
Insights
Hepatitis C virus (HCV) infection increases stroke risk. However, interferon-based therapy (IBT) significantly reduces this risk in chronic hepatitis C patients, offering a potential long-term benefit.
Area of Science:
- Hepatology
- Infectious Diseases
- Neurology
Background:
- Hepatitis C virus (HCV) infection is associated with increased risks of insulin resistance and carotid atherosclerosis.
- Understanding the link between HCV and cerebrovascular events is crucial for patient management.
Purpose of the Study:
- To investigate the association between HCV infection and the risk of stroke.
- To evaluate the impact of interferon-based therapy (IBT) on stroke risk in patients with chronic hepatitis C (CHC).
Main Methods:
- A retrospective cohort study involving 3113 newly diagnosed HCV patients and 12,452 matched controls.
- Analysis of stroke incidence using a 5-year follow-up from Taiwan's National Health Insurance Program.
- Hazard ratios (HR) were calculated, adjusting for confounding factors, comparing HCV patients to controls and IBT-treated HCV patients to non-IBT-treated patients.
Main Results:
- HCV infection was associated with a 23% increased risk of stroke (adjusted HR = 1.23, P = 0.008).
- Interferon-based therapy significantly reduced stroke risk in HCV patients by 61% (adjusted HR = 0.39, P = 0.039).
Conclusions:
- HCV infection is an independent risk factor for stroke.
- Interferon-based therapy demonstrates a protective effect against stroke in patients with chronic HCV infection.
Background:
Hepatitis C virus (HCV) infection has been linked to an increased risk of insulin resistance and carotid atherosclerosis.
Aim:
To investigate the association between HCV infection and stroke, and the effect of interferon-based therapy (IBT) on stroke risk in chronic hepatitis C (CHC) patients.
Methods:
We conducted a retrospective cohort study that followed up 3113 subjects with a newly detected HCV infection and 12 452 age- and gender-matched subjects without HCV infection selected from a random sample of 10(6) beneficiaries from the Taiwan National Health Insurance Program up to 5 years. Use of IBT was defined as treatment with interferon alpha, pegylated interferon alpha-2a or pegylated interferon alpha-2b for at least 3 months. The hazard ratio (HR) for newly detected stroke was calculated for subjects with HCV compared to those without HCV, and for IBT-treated HCV patients compared to non-IBT-treated HCV patients while adjusting for possible confounding factors.
Results:
The overall person-years of follow-up were 8624.11 in patients with HCV, 54,533.69 in patients without HCV, 666.65 in IBT-treated patients, and 7886.49 in nontreated patients. The multivariable-adjusted hazard ratio (HR) for newly detected stroke was 1.23 for subjects with HCV compared to the age- and sex-matched subjects without HCV (adjusted HR = 1.23, 95% CI = 1.06-1.42, P = 0.008). Moreover, use of IBT significantly reduced the risk of stroke in HCV patients (adjusted HR = 0.39, 95% CI = 0.16-0.95, P = 0.039) after adjusting for known prognostic factors.
Conclusions:
Interferon-based therapy may reduce the long-term risk of stroke in patients with chronic HCV infection.
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