Evidence map›Paper›PMID 42662852›Full record

ArticleThe Lancet regional health. Western Pacific2026

Unravelling HCV diversity and resistance in Viet Nam: a cross-sectional analysis.

Chau Le Ngoc, Haiting Chai, George Airey, Tanmay Das, Daisy Jennings, Fuqing Xu, Barnaby Flower, Mahdi Moradi Marjaneh, Leanne McCabe, Hung Le Manh and 15 more

Abstract read
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Article in The Lancet regional health. Western Pacific, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

25 authors.

Chau Le NgocOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Viet Nam.
Haiting ChaiNuffield Department of Medicine, University of Oxford, Oxford, UK.
George AireyNuffield Department of Medicine, University of Oxford, Oxford, UK.
Tanmay DasNuffield Department of Medicine, University of Oxford, Oxford, UK.
Daisy JenningsNuffield Department of Medicine, University of Oxford, Oxford, UK.
Fuqing XuNuffield Department of Medicine, University of Oxford, Oxford, UK.
Barnaby FlowerDepartment of Infectious Disease, Imperial College London, London, UK.
Mahdi Moradi MarjanehDepartment of Infectious Disease, Imperial College London, London, UK.
Leanne McCabeMRC Clinical Trial Unit at UCL, University College London, London, UK.
Hung Le ManhHospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
Chau Nguyen Van VinhHospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
Thuan Dang TrongOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Viet Nam.
Thach Pham NgocNational Hospital for Tropical Diseases, Ha Noi, Viet Nam.
Huong Vu Thi ThuNational Hospital for Tropical Diseases, Ha Noi, Viet Nam.
Guy E ThwaitesNuffield Department of Medicine, University of Oxford, Oxford, UK.
H Rogier van DoornOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Viet Nam.
Jeremy DayOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Viet Nam.
Evelyne KestelynOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Viet Nam.
Tan Le VanOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Viet Nam.
Motiur RahmanOxford University Clinical Research Unit (OUCRU), Ho Chi Minh City, Viet Nam.
Sarah PettMRC Clinical Trial Unit at UCL, University College London, London, UK.
Eleanor BarnesNuffield Department of Medicine, University of Oxford, Oxford, UK.
A Sarah WalkerMRC Clinical Trial Unit at UCL, University College London, London, UK.
Graham S CookeDepartment of Infectious Disease, Imperial College London, London, UK.
M Azim AnsariNuffield Department of Medicine, University of Oxford, Oxford, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Viet Nam has one of the world's most diverse hepatitis C virus (HCV) epidemics, dominated by genotype 6. Understanding pre-treatment resistance-associated substitutions (RASs) particularly in under-studied genotype 6 is important for informing resistance surveillance and supporting national HCV elimination strategies. We aimed to evaluate the landscape of viral diversity and baseline RASs relevant to currently used direct-acting antivirals (DAAs) in Viet Nam. Methods: We utilised whole-genome sequencing to analyse HCV isolates from a cohort of 1649 treatment-naïve patients enrolled in six clinical studies in Viet Nam between 2013 and 2023. The study assessed genotype and subtype distribution, associations with demographic and clinical variables, and prevalence of known and putative RASs in NS3, NS5A, and NS5B relevant to DAAs used in Viet Nam. Findings: Phylogenetic analysis revealed that genotype 6 was dominant (50.3%, 829/1649). We observed distinct geographical and demographic partitioning: genotype 2 was concentrated in the south and associated with older age and HIV co-infection, while genotype 3 was clustered in the north among younger males. Clinically relevant RASs were detected in 37.9% (617/1630) of patients, with the highest burden in NS5A region. Genotypes 2 and subtype 3b demonstrated a high prevalence of subtype-specific polymorphisms occurring at previously reported resistance-associated positions. Among genotype 6 infections, subtype 6a frequently carried L28F mutation (43.3%, 181/418), whereas subtype 6e demonstrated a low prevalence of previously reported clinical RASs. Interpretation: Viet Nam is characterised by a complex, genotype 6-predominant HCV epidemic with substantial subtype-specific baseline resistance diversity. The high prevalence of subtype-defining polymorphisms observed in several genotype 2 and subtype 3b lineages highlights the importance of continued molecular surveillance and may have implications for optimisation of DAA regimen selection and resistance monitoring strategies within highly diverse HCV populations. Funding: Wellcome Trust.

Indexed as

Direct-acting antiviralGenotypeHepatitis CResistance-associated substitutionSubtypeViet Nam

Identifiers

PMID42662852
PMCPMC13520911

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.