Key result
Interferon-based antiviral therapy for chronic HCV infection was associated with a lower risk of developing Parkinson disease compared to no treatment (HR 0.71; 95% CI 0.58-0.87).
Why the study?
HCV may be a risk factor for Parkinson disease, but prior studies had not considered HCV treatment, leaving the association between antiviral therapy and Parkinson disease incidence unclear.
Does interferon-based antiviral therapy reduce the risk of Parkinson disease in adult patients with chronic Hepatitis C virus infection?
Cohort (n=188,152)
Does interferon-based antiviral therapy reduce the risk of Parkinson disease in adult patients with chronic Hepatitis C virus infection?
Interferon-based antiviral therapy is associated with a lower incidence of Parkinson disease in patients with chronic HCV infection, supporting the hypothesis that HCV may be a risk factor for PD.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for antiviral neuroprotection; should not yet change HCV treatment practices.
IMPORTANCE: Epidemiologic evidence suggests that hepatitis C virus (HCV) could be a risk factor for Parkinson disease (PD), but treatment for HCV infection has never been considered in these studies; hence, the association between antiviral therapy and PD incidence has remained unclear. Understanding this association may help in developing strategies to reduce PD occurrence. OBJECTIVE: To identify the risk of PD development in patients with HCV infection receiving antiviral treatment and in patients not receiving this treatment. DESIGN, SETTING, AND PARTICIPANTS: This cohort study obtained claims data from the Taiwan National Health Insurance Research Database. Adult patients with a new HCV diagnosis with or without hepatitis per International Classification of Diseases, Ninth Revision, Clinical Modification codes and anti-PD medications from January 1, 2003, to December 31, 2013, were selected for inclusion. After excluding participants not eligible for analysis, the remaining patients (n = 188 152) were categorized into treated and untreated groups according to whether they received antiviral therapy. Propensity score matching was performed to balance the covariates across groups for comparison of main outcomes. This study was conducted from July 1, 2017, to December 31, 2017. MAIN OUTCOMES AND MEASURES: Development of PD was the main outcome. A Cox proportional hazards regression model was used to compare the risk of PD, and the hazard ratio (HR) was calculated at 1 year, 3 years, and 5 years after the index date and at the end of the cohort. RESULTS: A total of 188 152 patients were included in the analysis. An equal number (n = 39 936) and comparable characteristics of participants were retained in the treated group (with 17 970 female [45.0%] and a mean [SD] age of 52.8 [11.4] years) and untreated group (with 17 725 female [44.4%] and a mean [SD] age of 52.5 [12.9] years) after matching. The incidence density of PD was 1.00 (95% CI, 0.85-1.15) in the treated group and 1.39 (95% CI, 1.21-1.57) per 1000 person-years in the untreated group. The advantage of antiviral therapy reached statistical significance at the 5-year follow-up (HR, 0.75; 95% CI, 0.59-0.96), and this advantage continued to increase until the end of follow-up (HR, 0.71; 95% CI, 0.58-0.87). CONCLUSIONS AND RELEVANCE: Evidence suggested that the PD incidence was lower in patients with chronic HCV infection who received interferon-based antiviral therapy; this finding may support the hypothesis that HCV could be a risk factor for PD.
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Lin et al. (2019) conducted a cohort in Chronic Hepatitis C Virus Infection (n=188,152). Interferon-based antiviral therapy vs. No antiviral therapy was evaluated on Development of Parkinson disease (HR 0.71, 95% CI 0.58-0.87). Interferon-based antiviral therapy for chronic HCV infection was associated with a lower risk of developing Parkinson disease compared to no treatment (HR 0.71; 95% CI 0.58-0.87).
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