Hepatitis C virus eradication by direct-acting antiviral agents improves carotid atherosclerosis in patients with severe liver fibrosis
[Display omitted] •HCV eradication by direct-acting antiviral agents improves carotid atherosclerosis.•Atherosclerosis improvement is confirmed after stratification for cardiovascular risk factors.•Atherosclerosis improvement is observed in patients with and without cirrhosis. Recent studies suggest...
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Veröffentlicht in: | Journal of hepatology 2018-07, Vol.69 (1), p.18-24 |
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Sprache: | eng |
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•HCV eradication by direct-acting antiviral agents improves carotid atherosclerosis.•Atherosclerosis improvement is confirmed after stratification for cardiovascular risk factors.•Atherosclerosis improvement is observed in patients with and without cirrhosis.
Recent studies suggest an association between hepatitis C virus (HCV) infection and cardiovascular damage, including carotid atherosclerosis, with a possible effect of HCV clearance on cardiovascular outcomes. We aimed to examine whether HCV eradication by direct-acting antiviral agents (DAA) improves carotid atherosclerosis in HCV-infected patients with advanced fibrosis/compensated cirrhosis.
One hundred eighty-two consecutive patients with HCV and advanced fibrosis or compensated cirrhosis were evaluated. All patients underwent DAA-based antiviral therapy according to AISF/EASL guidelines. Intima-media thickness (IMT), carotid thickening (IMT ≥1 mm) and carotid plaques, defined as focal thickening of ≥1.5 mm at the level of the common carotid, were evaluated by ultrasonography (US) at baseline and 9–12 months after the end of therapy. Fifty-six percent of patients were male, mean age 63.1 ± 10.4 years, and 65.9% had compensated cirrhosis. One in five had diabetes, 14.3% were obese, 41.8% had arterial hypertension and 35.2% were smokers. At baseline, mean IMT was 0.94 ± 0.29 mm, 42.8% had IMT ≥1 mm, and 42.8% had carotid plaques.
All patients achieved a 12-week sustained virological response. IMT significantly decreased from baseline to follow-up (0.94 ± 0.29 mm vs. 0.81 ± 0.27, p |
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ISSN: | 0168-8278 1600-0641 |
DOI: | 10.1016/j.jhep.2018.02.015 |