» Articles » PMID: 36013545

Effect of Direct-Acting Antiviral Agents on Gastroesophageal Varices in Patients with Hepatitis C Virus-Related Cirrhosis

Overview
Publisher MDPI
Specialty General Medicine
Date 2022 Aug 26
PMID 36013545
Authors
Affiliations
Soon will be listed here.
Abstract

Aim: In patients with hepatitis C virus-related liver cirrhosis (LC) who achieve sustained virological responses (SVRs) through treatment with direct-acting antiviral agents (DAAs), it remains unclear whether there are improvements in gastroesophageal varices (GEVs) and portal hypertension. We investigated changes in liver function and GEVs that occurred after DAA therapy. Materials and Methods: We evaluated the medical records of 195 patients with hepatitis C virus-related LC who received DAAs. A total of 171 patients achieved SVRs, among whom 36 had GEVs before or after receiving DAA therapy. The liver function, fibrosis, and GEVs were re-evaluated every 6 months after receiving DAA therapy. The risk factors for progressive GEVs were investigated. Results: DAA therapy resulted in improvements in liver function (indicated by aspartate transaminase, alanine transaminase, and serum albumin levels) and fibrosis (indicated by type IV collagen levels and the Fibrosis-4 index). After receiving DAA therapy, 27 patients had stable GEVs and 9 had progressive GEVs. With respect to GEV grades before DAA therapy, there was a significant difference between patients with stable and progressive GEVs (p = 0.027). Presence of grade-2 GEVs before starting DAA therapy was a risk factor for GEV progression (odds ratio: 5.83; p = 0.04). Patients with grade-2 GEVs had significantly shorter progression-free periods than those with grade < 2 GEVs (p = 0.025). Conclusions: DAA therapy does not ameliorate GEVs. Furthermore, grade-2 GEVs can worsen after DAA therapy. Therefore, patients with GEVs of grades ≥ 2 should undergo endoscopic surveillance after receiving DAAs.

Citing Articles

Evolution of spontaneous portosystemic shunts over time and following aetiological intervention in patients with cirrhosis.

Vidal-Gonzalez J, Martinez J, Mulay A, Lopez M, Baiges A, Elmahdy A JHEP Rep. 2024; 6(2):100977.

PMID: 38283756 PMC: 10820312. DOI: 10.1016/j.jhepr.2023.100977.

References
1.
Lens S, Alvarado-Tapias E, Marino Z, Londono M, Llop E, Martinez J . Effects of All-Oral Anti-Viral Therapy on HVPG and Systemic Hemodynamics in Patients With Hepatitis C Virus-Associated Cirrhosis. Gastroenterology. 2017; 153(5):1273-1283.e1. DOI: 10.1053/j.gastro.2017.07.016. View

2.
Tada T, Kumada T, Toyoda H, Mizuno K, Sone Y, Kataoka S . Improvement of liver stiffness in patients with hepatitis C virus infection who received direct-acting antiviral therapy and achieved sustained virological response. J Gastroenterol Hepatol. 2017; 32(12):1982-1988. DOI: 10.1111/jgh.13788. View

3.
Kanwal F, Kramer J, Asch S, Chayanupatkul M, Cao Y, El-Serag H . Risk of Hepatocellular Cancer in HCV Patients Treated With Direct-Acting Antiviral Agents. Gastroenterology. 2017; 153(4):996-1005.e1. DOI: 10.1053/j.gastro.2017.06.012. View

4.
Miyaaki H, Ichikawa T, Taura N, Miuma S, Isomoto H, Nakao K . Endoscopic management of esophagogastric varices in Japan. Ann Transl Med. 2014; 2(5):42. PMC: 4200683. DOI: 10.3978/j.issn.2305-5839.2014.05.02. View

5.
Garcia-Tsao G, Sanyal A, Grace N, Carey W . Prevention and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. Hepatology. 2007; 46(3):922-38. DOI: 10.1002/hep.21907. View