Key result
Sustained virologic response after interferon therapy fails to reduce new-onset depression risk versus non-SVR.
Why the study?
The impact of interferon-based therapy after achieving sustained virologic response on the long-term risk of depressive disorders in chronic hepatitis C patients remains unclear.
Does achieving sustained virologic response (SVR) after interferon-based therapy reduce the incidence of new-onset depressive disorder in patients with chronic hepatitis C?
Cohort (n=5,550)
Yes
Does achieving sustained virologic response (SVR) after interferon-based therapy reduce the incidence of new-onset depressive disorder in patients with chronic hepatitis C?
Absolute Event Rate: 18% vs 16.7%
Achieving sustained virologic response after interferon-based therapy for chronic hepatitis C does not significantly reduce the long-term risk of new-onset depression, highlighting the need for ongoing psychiatric monitoring.
SVR after IFN-based HCV therapy does not reduce long-term depression risk; leaves open whether modern DAAs or targeted monitoring alter neuropsychiatric trajectories.
BACKGROUND: Chronic hepatitis C virus (HCV) infection is associated with an increased risk of neuropsychiatric disorders, including depression. However, the impact of interferon (IFN)-based therapy, after achieving a sustained virologic response (SVR), on the long-term risk of depressive disorders remains unclear. Thus, we evaluated the incidence of new-onset depression and the impact of risk factors on patients with chronic hepatitis C following antiviral therapy. METHODS: This nationwide, real-world cohort included a total of 5550 patients with HCV infection who received IFN-based therapy between 2003 and 2014. The primary outcome was the incidence of new-onset depressive disorder. The cumulative incidence of depressive disorders was analyzed using Gray's competing risk method, and Cox proportional hazards models were used to identify independent risk factors. RESULTS: During a mean follow-up of 4.07 years, the incidence of new-onset depression was 18.0 % in patients with SVR and 16.7 % in patients with non-SVR. Achieving SVR did not significantly reduce the risk of depression across the various subgroups. Multivariate analysis identified older age (≥45 years, HR = 1.32, 95 % CI: 1.10-1.57, P = 0.003) and female sex (HR = 1.29, 95 % CI: 1.11-1.49, P = 0.0007) as independent risk factors for depression, but only in patients with SVR. CONCLUSION: Our findings highlight the need for long-term psychiatric monitoring in patients with HCV infection after treatment, particularly in high-risk subgroups. Further studies involving direct-acting antiviral-treated cohorts with extended follow-up periods are required to validate these findings.
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Hu et al. (2025) conducted a cohort in Chronic hepatitis C (n=5,550). Sustained virologic response (SVR) vs. Non-SVR was evaluated on Incidence of new-onset depressive disorder. Achieving a sustained virologic response after interferon-based therapy did not significantly reduce the risk of new-onset depression compared to non-SVR (18.0% vs 16.7%).
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