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Drug Resistance Profile and Clinical Features for Hepatitis C Patients Experiencing DAA Failure in Taiwan

Authors :
Chun-Ming Hong
You-Yu Lin
Chun-Jen Liu
Ya-Yun Lai
Shiou-Hwei Yeh
Hung-Chih Yang
Jia-Horng Kao
Shih-Jer Hsu
Yi-Hsiang Huang
Sheng-Shun Yang
Hsing-Tao Kuo
Pin-Nan Cheng
Ming-Lung Yu
Pei-Jer Chen
Source :
Viruses, Vol 13, Iss 11, p 2294 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

About 4% of the population in Taiwan are seropositive for anti-HCV Ab and 70% with HCV RNA. To address this high chronic hepatitis C disease load, Taiwan National Health Insurance started reimbursing genotype-specific DAAs in 2017 and pangenotype DAAs in mid-2018. With a 97% SVR12 rate, there were still 2–3% of patients that failed to clear HCV. To understand the causes of DAA failure in Taiwan, we conducted a multi-center, clinical, and virologic study. A total of 147 DAA-failure patients were recruited, and we searched HCV NS3/4A, NS5A and NS5B for known resistance-associated substitutions (RASs) by population sequencing, and conducted whole genome sequencing (WGS) for those without known RASs. A total of 107 patients received genotype-specific DAAs while 40 had pangenotype DAAs. Clinically, the important cause of failure is poor adherence. Virologically, common RASs in genotype-specific DAAs were NS5A-L31, NS5A-Y93, and NS5B-C316, while common RASs in pangenotype DAAs were NS5A-L31, NS5A-A/Q/R30, and NS5A-Y93. Additionally, new amino acid changes were found by WGS. Finally, we identified 12 cases with inconsistent baseline and post-treatment HCV genotypes, which is suggestive of re-infection rather than treatment failure. Our study described the drug resistance profile for DAA failure in Taiwan, showing differences from other countries.

Details

Language :
English
ISSN :
19994915
Volume :
13
Issue :
11
Database :
Directory of Open Access Journals
Journal :
Viruses
Publication Type :
Academic Journal
Accession number :
edsdoj.4771619952644a0e85cb664e74106a9b
Document Type :
article
Full Text :
https://doi.org/10.3390/v13112294