Evidence map›Paper›PMID 41226685›Full record

ArticleInternational journal of molecular sciences2025

Deep Sequencing Analysis of Hepatitis C Virus Subtypes and Resistance-Associated Substitutions in Genotype 4 Patients Resistant to Direct-Acting Antiviral (DAA) Treatment in Egypt.

Damir Garcia-Cehic, Asmaa Mosbeh, Heba A Gad, Asmaa Ibrahim Gomaa, Marta Ibañez Lligoña, Josep Gregori, Sergi Colomer-Castell, Carolina Campos, Francisco Rodriguez-Frias, Juan Ignacio Esteban and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Damir Garcia-CehicDepartment of Radiation Oncology, University of Cincinnati, College of Medicine, Cincinnati, OH 45267, USA.ORCID 0000-0002-0009-038X
Asmaa MosbehDepartment of Pathology, National Liver Institute, Menoufia University, Menoufia Governorate 6131567, Egypt.
Heba A GadSustainable Sciences Institute Collaborative Research Center, Menoufia University, Menoufia Governorate 6131567, Egypt.ORCID 0000-0001-7469-1244
Asmaa Ibrahim GomaaDepartment of Hepatology, National Liver Institute, Menoufia University, Menoufia Governorate 6131567, Egypt.ORCID 0000-0001-9376-4461
Marta Ibañez LligoñaLiver Diseases-Viral Hepatitis, Liver Unit, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.ORCID 0000-0003-3428-2168
Josep GregoriLiver Diseases-Viral Hepatitis, Liver Unit, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.ORCID 0000-0002-4253-8015
Sergi Colomer-CastellLiver Diseases-Viral Hepatitis, Liver Unit, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.
Carolina CamposLiver Diseases-Viral Hepatitis, Liver Unit, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.ORCID 0000-0002-0132-7027
Francisco Rodriguez-FriasLiver Diseases-Viral Hepatitis, Liver Unit, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.ORCID 0000-0002-9128-7013
Juan Ignacio EstebanLiver Diseases-Viral Hepatitis, Liver Unit, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.
Mohamed S KohlaSustainable Sciences Institute Collaborative Research Center, Menoufia University, Menoufia Governorate 6131567, Egypt.
Mohamed Helmy Abdel-RahmanDepartment of Pathology, National Liver Institute, Menoufia University, Menoufia Governorate 6131567, Egypt.ORCID 0000-0002-9493-7894
Josep QuerLiver Diseases-Viral Hepatitis, Liver Unit, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.ORCID 0000-0003-0014-084X

Funding

Centre for Industrial Technological Development IDI-20200297Gilead GLD21/00006Gilead Corporate 04562La Caixa" Foundation 100010434Spanish Ministry of Economy and Business IDI-20200297Spanish Ministry of Education FPU21/04150
6 · The paper itself

Abstract

Egypt has the highest global prevalence of hepatitis C virus (HCV), with genotype 4 (G4) in over 94% of cases. Direct-acting antivirals (DAAs) yield sustained virologic response (SVR) rates above 95%. Second-generation DAAs are recommended for patients with virological failure, achieving over 90% eradication. This study aimed to classify and evaluate the pattern of HCV resistance-associated substitutions (RASs) in patients who failed DAA treatment in Egypt. A total of 1778 chronically infected HCV patients from Egypt's Nile Delta were enrolled (2016-2018). Among them, 37 relapsed, and high-quality serum samples from 22 patients were available, including 6 cases with pre- and post-treatment samples. Next-generation sequencing (NGS) was performed for HCV subtyping and RAS identification. Among the 22 analyzed cases, 21 (95.4%) were G4: 11 were classified as subtype G4a, seven G4o, and three G4m. One patient (4.5%) was identified as G1g. One case shifted from G4a pre- to G4o post-treatment, suggesting reinfection. The RAS pattern in rare G4 subtypes (G4m/G4o) differs from the G4a subtype. The combination of L28M/L30S mutations was detected in 8/11 G4a samples; in contrast, RASs in G4o were characterized by T30S or Y93C/H/N/S substitutions. Notably, some substitutions identified as RASs may represent fixed polymorphisms in regional viral populations, such as those in Egypt's Nile Delta. HCV subtypes significantly influence the RAS pattern, particularly within the NS5A region, after DAA-treatment failure. The RAS pattern differs among G4 subtypes, particularly in rare ones, predisposing patients to resistance and underscoring the importance of NGS in regional populations to optimize treatment strategies.

Indexed as

Antiviral AgentsDrug Resistance, ViralHepacivirusHepatitis C, ChronicAdultAmino Acid SubstitutionEgyptFemaleGenotypeHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutationViral Nonstructural ProteinsAntiviral AgentsViral Nonstructural ProteinsDAAdeep sequencingHCV subtypesNS5ARAS

Identifiers

PMID41226685
PMCPMC12609098

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.