Evidence map›Paper›PMID 23711895›Full record

ArticleThe Journal of antimicrobial chemotherapy2013

Low frequency of genotypic resistance in HIV-1-infected patients failing an atazanavir-containing regimen: a clinical cohort study.

David I Dolling, David T Dunn, Katherine A Sutherland, Deenan Pillay, Jean L Mbisa, Chris M Parry, Frank A Post, Caroline A Sabin, Patricia A Cane, UK HIV Drug Resistance Database (UKHDRD) and 1 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. HIV and Drug-Resistant Subtypes.Microorganisms · 2023
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Observational
  8. HIV-1 drug resistance and resistance testing.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2016
    Review
  9. Article
  10. Recent trends in HIV-1 drug resistance.Current opinion in virology · 2013
    Review
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

11 authors at 5 institutions in 2 countries.

David I DollingMedical Research Council Clinical Trials Unit, London, UK.
David T Dunn
Katherine A Sutherland
Deenan Pillay
Jean L Mbisa
Chris M Parry
Frank A Post
Caroline A Sabin
Patricia A Cane
UK HIV Drug Resistance Database (UKHDRD)
UK Collaborative HIV Cohort Study (UK CHIC)
Public Health England · GBMedical Research Council · GBUniversity College London · GBKing's College London · GBUganda Virus Research Institute · UG

Funding

Medical Research Council G0000199Medical Research Council G0600337Medical Research Council G0900274Medical Research Council MC_UU_12023/15Medical Research Council MR/K006584/1
6 · The paper itself

Abstract

objectivesTo determine protease mutations that develop at viral failure for protease inhibitor (PI)-naive patients on a regimen containing the PI atazanavir.

methodsResistance tests on patients failing atazanavir, conducted as part of routine clinical care in a multicentre observational study, were randomly matched by subtype to resistance tests from PI-naive controls to account for natural polymorphisms. Mutations from the consensus B sequence across the protease region were analysed for association and defined using the IAS-USA 2011 classification list.

resultsFour hundred and five of 2528 (16%) patients failed therapy containing atazanavir as a first PI over a median (IQR) follow-up of 1.76 (0.84-3.15) years and 322 resistance tests were available for analysis. Recognized major atazanavir mutations were found in six atazanavir-experienced patients (P < 0.001), including I50L and N88S. The minor mutations most strongly associated with atazanavir experience were M36I, M46I, F53L, A71V, V82T and I85V (P < 0.05). Multiple novel mutations, I15S, L19T, K43T, L63P/V, K70Q, V77I and L89I/T/V, were also associated with atazanavir experience.

conclusionsViral failure on atazanavir-containing regimens was not common and major resistance mutations were rare, suggesting that adherence may be a major contributor to viral failure. Novel mutations were described that have not been previously documented.

Indexed as

Drug Resistance, ViralAdultAnti-HIV AgentsAtazanavir SulfateCohort StudiesFemaleHIV-1HIV InfectionsHIV ProteaseHumansMaleMedication AdherenceMiddle AgedMutation, MissenseMutation RateOligopeptidesAnti-HIV AgentsAtazanavir SulfateHIV ProteaseOligopeptidesPyridinesdrug resistance mutationsHIVnaive patientsprotease inhibitorsvirological failure

Identifiers

PMID23711895
PMCPMC3772741
OpenAlexW2143657151

What OpenQuestion holds

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LicenceCC BY-NC
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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.