Evidence map›Paper›PMID 29895871›Full record

Observational studyScientific reports2018

Prevalence of Single and Multiple Natural NS3, NS5A and NS5B Resistance-Associated Substitutions in Hepatitis C Virus Genotypes 1-4 in Italy.

Ada Bertoli, Maria Chiara Sorbo, Marianna Aragri, Ilaria Lenci, Elisabetta Teti, Ennio Polilli, Velia Chiara Di Maio, Laura Gianserra, Elisa Biliotti, Chiara Masetti and 25 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

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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

35 authors.

Ada BertoliDepartment Experimental Medicine and Surgery, University of Rome "Tor Vergata", 00133, Rome, Italy.ORCID 0000-0003-0663-2503
Maria Chiara SorboDepartment Experimental Medicine and Surgery, University of Rome "Tor Vergata", 00133, Rome, Italy.
Marianna AragriDepartment Experimental Medicine and Surgery, University of Rome "Tor Vergata", 00133, Rome, Italy.
Ilaria LenciHepatology Unit, University Hospital of Rome "Tor Vergata", 00133, Rome, Italy.
Elisabetta TetiInfectious Diseases Unit, University Hospital of Rome "Tor Vergata", 00133, Rome, Italy.
Ennio PolilliInfectious Diseases Unit, Pescara General Hospital, 65124, Pescara, Italy.
Velia Chiara Di MaioDepartment Experimental Medicine and Surgery, University of Rome "Tor Vergata", 00133, Rome, Italy.
Laura GianserraInfectious Diseases Unit, Sant'Andrea Hospital - "Sapienza" University, 00189, Rome, Italy.
Elisa BiliottiTropical Diseases, Umberto I Hospital -"Sapienza" University, 00161, Rome, Italy.
Chiara MasettiHepatology Unit, University Hospital of Rome "Tor Vergata", 00133, Rome, Italy.
Carlo F Magni1st Division of Infectious Diseases, ASST Fatebenefratelli Sacco, 20157, Milan, Italy.
Sergio BabudieriClinical and Experimental Medicine, University of Sassari, 07100, Sassari, Italy.
Laura A NicoliniInfectious Diseases Unit, IRCCS AOU San Martino - IST, 16132, Genoa, Italy.
Martina MilanaHepatology Unit, University Hospital of Rome "Tor Vergata", 00133, Rome, Italy.
Pierluigi CacciatoreInfectious Diseases Unit, Pescara General Hospital, 65124, Pescara, Italy.
Loredana SarmatiInfectious Diseases Unit, University Hospital of Rome "Tor Vergata", 00133, Rome, Italy.
Adriano PellicelliHepatology Unit, San Camillo Forlanini Hospital, 00151, Rome, Italy.
Stefania PaolucciMolecular Virology, Fondazione IRCCS Policlinico San Matteo, 27100, Pavia, Italy.
Antonio CraxìGastroenterology, "P. Giaccone" University Hospital, 90127, Palermo, Italy.
Filomena MoriscoGastroenterology, "Federico II" University, 80131, Naples, Italy.
Valeria Pace PalittiHepatology Unit, Pescara General Hospital, 65124, Pescara, Italy.
Massimo SicilianoGastroenterology, Catholic University of Rome, 00168, Rome, Italy.
Nicola CoppolaInfectious Diseases Unit, "L. Vanvitelli" University of Campania, 80138, Naples, Italy.
Nerio IapadreInfectious Diseases Unit, S. Salvatore Hospital, 67100, L'Aquila, Italy.
Massimo PuotiInfectious Diseases Unit, Niguarda Ca' Granda Hospital, 20162, Milan, Italy.
Giuliano Rizzardini1st Division of Infectious Diseases, ASST Fatebenefratelli Sacco, 20157, Milan, Italy.
Gloria TalianiTropical Diseases, Umberto I Hospital -"Sapienza" University, 00161, Rome, Italy.
Caterina PasquazziInfectious Diseases Unit, Sant'Andrea Hospital - "Sapienza" University, 00189, Rome, Italy.
Massimo AndreoniInfectious Diseases Unit, University Hospital of Rome "Tor Vergata", 00133, Rome, Italy.
Giustino ParrutiInfectious Diseases Unit, Pescara General Hospital, 65124, Pescara, Italy.
Mario AngelicoHepatology Unit, University Hospital of Rome "Tor Vergata", 00133, Rome, Italy.
Carlo Federico PernoHaematology and Oncohematology, University of Milan, 20122, Milan, Italy.
Valeria CentoDepartment Experimental Medicine and Surgery, University of Rome "Tor Vergata", 00133, Rome, Italy. valeriacento@gmail.com.
Francesca Ceccherini-SilbersteinDepartment Experimental Medicine and Surgery, University of Rome "Tor Vergata", 00133, Rome, Italy.
HCV Virology Italian Resistance Network (VIRONET-C)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural resistance-associated substitutions (RASs) are reported with highly variable prevalence across different HCV genotypes (GTs). Frequency of natural RASs in a large Italian real-life cohort of patients infected with the 4 main HCV-GTs was investigated. NS3, NS5A and NS5B sequences were analysed in 1445 HCV-infected DAA-naïve patients. Sanger-sequencing was performed by home-made protocols on 464 GT1a, 585 GT1b, 92 GT2c, 199 GT3a, 16 GT4a and 99 GT4d samples. Overall, 20.7% (301/1455) of patients showed natural RASs, and the prevalence of multiclass-resistance was 7.3% (29/372 patients analysed). NS3-RASs were particularly common in GT1a and GT1b (45.2-10.8%, respectively), mainly due to 80K presence in GT1a (17%). Almost all GTs showed high prevalence of NS5A-RASs (range: 10.2-45.4%), and especially of 93H (5.1%). NS5A-RASs with fold-change >100x were detected in 6.8% GT1a (30H/R-31M-93C/H), 10.3% GT1b (31V-93H), 28.4% GT2c (28C-31M-93H), 8.5% GT3a (30K-93H), 45.5% GT4a (28M-30R-93H) and 3.8% GT4d (28V-30S-93H). Sofosbuvir RAS 282T was never detected, while the 159F and 316N RASs were found in GT1b (13.4-19.1%, respectively). Natural RASs are common in Italian patients infected with HCV-GTs 1-4. High prevalence of clinically-relevant RASs (such as Y93H) supports the appropriateness of HCV resistance-test to properly guide DAA-based therapy.

Indexed as

GenotypeAdultAgedDEAD-box RNA HelicasesDrug Resistance, ViralFemaleHepacivirusHepatitis CHumansItalyMaleMiddle AgedNucleoside-TriphosphatasePrevalenceRNA-Dependent RNA PolymeraseSerine EndopeptidasesDEAD-box RNA HelicasesNS3 protein, hepatitis C virusNS-5 protein, hepatitis C virusNucleoside-TriphosphataseRNA-Dependent RNA PolymeraseSerine EndopeptidasesViral Nonstructural ProteinsViral Proteases

Identifiers

PMID29895871
PMCPMC5997636

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Registered trials

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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.