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Are Direct-Acting Antivirals Effective and Safe for Hepatitis C Patients with Arterial Hypertension? Evidence from a
Michał Brzdęk1, Piotr Rzymski2, Dorota Zarębska-Michaluk3
1Collegium Medicum, Jan Kochanowski University, 25-317 Kielce, Poland.
Insights
Direct-acting antivirals (DAAs) are safe and effective for treating hepatitis C virus (HCV) infection in patients with arterial hypertension (AH). Early detection and treatment of HCV in this population are crucial for better health outcomes.
Area of Science:
- Hepatology
- Cardiology
- Infectious Diseases
Background:
- Arterial hypertension (AH) and hepatitis C virus (HCV) infection share a bidirectional relationship, impacting liver and cardiovascular health.
- Limited data exist on direct-acting antiviral (DAA) efficacy and safety in hypertensive HCV patients.
Purpose of the Study:
- To evaluate the effectiveness and safety of DAAs in treating HCV among patients with arterial hypertension.
- To identify factors influencing treatment outcomes in this specific patient group.
Main Methods:
- Retrospective analysis of the EpiTer-2 project (2015-2023) involving 18,968 HCV-infected patients treated with DAAs.
- Comparison of outcomes between 5976 patients with AH and those without AH.
Main Results:
- High and comparable sustained virologic response (SVR) rates were observed in both AH (94.8% ITT, 97.6% PP) and non-AH groups (94.2% ITT, 97.6% PP).
- Arterial hypertension was not an independent predictor of treatment failure.
- Predictors of failure included HCV genotype 3, decompensated liver function, cirrhosis, thrombocytopenia, and specific DAA regimens.
Conclusions:
- DAAs demonstrate significant safety and efficacy in HCV patients with arterial hypertension.
- Early diagnosis and treatment of HCV are vital for this comorbid population.
- Potential drug-drug interactions with antihypertensive medications appear minimal in clinical practice.
Abstract:
Background/Objectives: Arterial hypertension (AH) and hepatitis C virus (HCV) infection are interlinked, with AH increasing the risk of severe liver disease and HCV contributing to cardiovascular issues. Treating HCV in hypertensive patients is critical, though data on direct-acting antivirals (DAAs) in this group remain limited. Methods: This retrospective study evaluated the effects of DAAs in AH patients with HCV using data from the 2015-2023 EpiTer-2 project, a multicenter study in Poland. Results: Among the 18,968 HCV-infected DAA-treated patients, 5976 had AH. These patients were older, predominantly women, and had higher rates of obesity, comorbidities, cirrhosis, hepatocellular carcinoma, and genotype 1b infection. Sustained virologic response rates were high and comparable between the AH and non-AH groups in the intent-to-treat (94.8% vs. 94.2%) and per-protocol analyses (97.6% vs. 97.6%). AH was not independently associated with treatment failure (OR 0.87, 95% CI: 0.69-1.10). Predictors of failure included genotype 3, decompensated liver function, cirrhosis, thrombocytopenia, and treatment with asunaprevir + daclatasvir. While therapy discontinuation was more common in the AH patients, most completed treatment, with fatigue being the most frequent adverse event. Although not directly evaluated, the overall safety outcomes suggest that potential drug-drug interactions with antihypertensive therapies are unlikely to have a major clinical impact in routine practice. Conclusions: This study highlights the safety and efficacy of DAAs in AH patients and emphasizes the importance of early HCV detection and treatment in this population.
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