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.

Viruses
|July 28, 2026
PubMed

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.

Related Concept Videos

Hepatitis01:25

Hepatitis

Hepatitis is an inflammatory condition of the liver most commonly caused by hepatotropic viruses (A–E), though non-infectious causes such as alcohol and drugs also exist.Hepatitis AHepatitis A virus (HAV) is a non-enveloped RNA virus of the Picornaviridae family. It is primarily transmitted via the fecal-oral route, typically through ingestion of contaminated food or water. After ingestion, HAV enters the bloodstream through the oropharynx or intestinal epithelium and reaches the liver. The...
Antihypertensive Drugs: Direct Renin Inhibitors01:25

Antihypertensive Drugs: Direct Renin Inhibitors

The renin-angiotensin-aldosterone system (RAAS) is an intricate physiological pathway involving numerous enzymes and hormones, including renin, angiotensin-converting enzyme (ACE), angiotensin I and II, and aldosterone. Imbalances within this system increase the production of angiotensin II and aldosterone. Increased angiotensin II levels promote vasoconstriction and blood pressure elevation. Concurrently, higher aldosterone levels stimulate sodium and water reabsorption in the kidneys,...
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Antihypertensive Drugs: Angiotensin II Receptor Blockers01:30

Antihypertensive Drugs: Angiotensin II Receptor Blockers

In the renin-angiotensin-aldosterone system, a hormone called angiotensin II plays a crucial role. It binds to the AT1 receptors in vascular smooth muscles coupled with Gq proteins. The activation of these receptors activates an enzyme called phospholipase C, which releases two molecules: inositol trisphosphate and diacylglycerol. These molecules cause a chain reaction that leads to the phosphorylation of myosin light chains and promotes interaction between actin and myosin, leading to smooth...
Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors01:28

Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors

Phosphodiesterase 5 (PDE5) inhibitors are potent enzymes that function to hydrolyze cyclic nucleotides to their corresponding 5' monophosphates. Their unique biochemical properties have been applied in treating Pulmonary Arterial Hypertension (PAH).
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...