Key result
HCV eradication with DAAs is linked to a ~7% reduction in carotid IMT and improved ABI.
Why the study?
Chronic HCV infection is linked to cardiovascular disease, but whether viral eradication with direct-acting antivirals benefits carotid atherosclerosis and peripheral artery disease required evaluation.
Does viral eradication by direct-acting antivirals improve carotid atherosclerosis and peripheral artery disease in patients with chronic HCV infection?
Cohort (n=168)
No
Does viral eradication by direct-acting antivirals improve carotid atherosclerosis and peripheral artery disease in patients with chronic HCV infection?
Absolute Event Rate: 1.13% vs 1.22%
p-value: p=<0.001
HCV eradication with direct-acting antivirals improves surrogate markers of carotid atherosclerosis and peripheral artery disease, particularly in patients with advanced liver fibrosis.
Supports vascular surrogate improvement after HCV eradication in advanced fibrosis; hypothesis-generating for cardiovascular outcomes.
INTRODUCTION: Recent research points to a link between chronic hepatitis C virus (HCV) infection and cardiovascular disease, especially carotid atherosclerosis, and suggests that HCV clearance may impact cardiovascular outcomes. AIM: To determine if viral eradication by the new oral direct-acting antiviral (DAA) agents has benefit regarding carotid atherosclerosis, peripheral artery disease (PAD), steatosis, and liver fibrosis. PATIENTS, MATERIALS AND METHODS: We conducted a prospective study on 168 patients diagnosed with chronic HCV infection or HCV-related cirrhosis. They were all treated with DAAs, with sustained virological response (SVR). Laboratory data, vibration-controlled transient elastography (VCTE), carotid intima-media thickness (IMT) measurement, and ankle-brachial index (ABI) were recorded in all patients. RESULTS: We found an average IMT of 1.22±0.2 mm, with a variance range from 1.14±0.19 mm in the mild and moderate fibrosis (≤F2) group to 1.29±0.25 mm in the severe fibrosis (≥F3) group. Also, patients with severe fibrosis (≥F3) present a more critical decrease of IMT values, with the carotid thickness affecting only 18.2% of individuals in the follow-up period. At the baseline, the best values of ABI were recorded in patients having F1-F2 fibrosis stage (mean value 1.02±0.19). Instead, in the group with severe fibrosis, the average value of ABI was lower (0.91±0.16) at the baseline, with a significant increase at SVR evaluation (p<0.001). CONCLUSIONS: Our research highlights the beneficial effect of viral eradication on both carotid atherosclerosis and PAD, especially in those with advanced fibrosis and cirrhosis.
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Cuciureanu et al. (2024) conducted a cohort in Chronic hepatitis C virus infection (n=168). Direct-acting antivirals (DAAs) vs. Baseline (pre-treatment) was evaluated on Carotid intima-media thickness (IMT) (p=<0.001). Eradication of hepatitis C virus with direct-acting antivirals significantly reduced carotid intima-media thickness from 1.22 mm to 1.13 mm and improved ankle-brachial index.
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