Evidence map›Paper›PMID 33893696›Full record

ArticleJournal of viral hepatitis2021

Global prevalence and phylogeny of hepatitis B virus (HBV) drug and vaccine resistance mutations.

Jolynne Mokaya, Tetyana I Vasylyeva, Eleanor Barnes, M Azim Ansari, Oliver G Pybus, Philippa C Matthews

Open access · hybridAbstract read
In one paragraph

Article in Journal of viral hepatitis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

13 citing papers in PubMed, 25 citations in OpenAlex.

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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

6 authors at 5 institutions in 2 countries.

Jolynne MokayaNuffield Department of Medicine, Oxford, UK.
Tetyana I VasylyevaDivision of Infectious Diseases & Global Public Health, Department of Medicine, University of California, San Diego, CA, USA.
Eleanor BarnesNuffield Department of Medicine, Oxford, UK.
M Azim AnsariNuffield Department of Medicine, Oxford, UK.
Oliver G PybusDepartment of Zoology, University of Oxford, Oxford, UK.
Philippa C MatthewsNuffield Department of Medicine, Oxford, UK.
University of Oxford · GBJohn Radcliffe Hospital · GBNuffield Health · GBNuffield Orthopaedic Centre · GBUniversity of California, San Diego · US

Funding

Branco Weiss Fellowship - Society in ScienceLeverhulme TrustWellcome Trust
6 · The paper itself

Abstract

Vaccination and anti-viral therapy with nucleos(t)ide analogues (NAs) are key approaches to reducing the morbidity, mortality and transmission of hepatitis B virus (HBV) infection. However, the efficacy of these interventions may be reduced by the emergence of drug resistance-associated mutations (RAMs) and/or vaccine escape mutations (VEMs). We have assimilated data on the global prevalence and distribution of HBV RAMs/VEMs from publicly available data and explored the evolution of these mutations. We analysed sequences downloaded from the HBV Database and calculated prevalence of 41 RAMs and 38 VEMs catalogued from published studies. We generated maximum likelihood phylogenetic trees and used treeBreaker to investigate the distribution and estimated the age of selected mutations across tree branches. RAM M204I/V had the highest prevalence, occurring in 3.8% (109/2838) of all HBV sequences in our data set, and a significantly higher rate in genotype C at 5.4% (60/1102, p = 0.0007). VEMs had an overall prevalence of 1.3% (37/2837) and had the highest prevalence in genotype C and in Asia at 2.2% (24/1102; p = 0.002) and 1.6% (34/2109; p = 0.009), respectively. Phylogenetic analysis suggested that RAM/VEMs can arise independently of treatment/vaccine exposure. In conclusion, HBV RAMs/VEMs have been found globally and across genotypes, with the highest prevalence observed in genotype C. Screening for genotype and for resistance-associated mutations may help to improve stratified patient treatment. As NAs and HBV vaccines are increasingly being deployed for HBV prevention and treatment, monitoring for resistance and advocating for better treatment regimens for HBV remains essential.

Indexed as

Hepatitis B, ChronicPharmaceutical PreparationsAntiviral AgentsDNA, ViralDrug Resistance, ViralGenotypeHepatitis B VaccinesHepatitis B virusHumansMutationPhylogenyPrevalenceAntiviral AgentsDNA, ViralHepatitis B VaccinesPharmaceutical PreparationsAfricaentecavirepidemiologyHBVHBV vaccinelamivudineNAsNUCspreventionRAMsresistanceTDFtenofovirtherapy

Identifiers

PMID33893696
PMCPMC8581767
OpenAlexW3091915967

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.