Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital

Global evolutionary analysis of chronic hepatitis C patients revealed significant effect of baseline viral resistance, including novel non-target sites, for DAA-based treatment and retreatment outcome

Research output: Contribution to journalJournal articleResearchpeer-review


  1. Hepatitis E during pregnancy: Maternal and foetal case-fatality rates and adverse outcomes—A systematic review

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Low compliance with hepatocellular carcinoma screening guidelines in hepatitis B/C virus co-infected HIV patients with cirrhosis

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Hepatocellular carcinoma in patients with chronic hepatitis C and cirrhosis in Denmark: a nationwide cohort study

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Historical epidemiology of hepatitis C virus (HCV) in selected countries

    Research output: Contribution to journalJournal articleResearchpeer-review

View graph of relations

Direct-acting antivirals (DAAs) have proven highly effective against chronic hepatitis C virus (HCV) infection. However, some patients experience treatment failure, associated with resistance-associated substitutions (RASs). Our aim was to investigate the complete viral coding sequence in hepatitis C patients treated with DAAs to identify RASs and the effects of treatment on the viral population. We selected 22 HCV patients with sustained virologic response (SVR) to match 21 treatment-failure patients in relation to HCV genotype, DAA regimen, liver cirrhosis and previous treatment experience. Viral-titre data were compared between the two patient groups, and HCV full-length open reading frame deep-sequencing was performed. The proportion of HCV NS5A-RASs at baseline was higher in treatment-failure (82%) than matched SVR patients (25%) (p = .0063). Also, treatment failure was associated with slower declines in viraemia titres. Viral population diversity did not differ at baseline between SVR and treatment-failure patients, but failure was associated with decreased diversity probably caused by selection for RAS. The NS5B-substitution 150V was associated with sofosbuvir treatment failure in genotype 3a. Further, mutations identified in NS2, NS3-helicase and NS5A-domain-III were associated with DAA treatment failure in genotype 1a patients. Six retreated HCV patients (35%) experienced 2nd treatment failure; RASs were present in 67% compared to 11% with SVR. In conclusion, baseline RASs to NS5A inhibitors, but not virus population diversity, and lower viral titre decline predicted HCV treatment failure. Mutations outside of the DAA targets can be associated with DAA treatment failure. Successful DAA retreatment in patients with treatment failure was hampered by previously selected RASs.

Original languageEnglish
JournalJournal of Viral Hepatitis
Issue number2
Pages (from-to)302-316
Publication statusPublished - Feb 2021

Bibliographical note

© 2020 John Wiley & Sons Ltd.

    Research areas

  • direct&#8208, acting antivirals, genome&#8208, wide association studies, hepatitis C virus, next&#8208, generation sequencing, resistance&#8208, associated substitution, treatment failure

ID: 61309448