Evidence map›Paper›PMID 29977967›Full record

ArticleOpen forum infectious diseases2018

Impact of the M184V Resistance Mutation on Virological Efficacy and Durability of Lamivudine-Based Dual Antiretroviral Regimens as Maintenance Therapy in Individuals With Suppressed HIV-1 RNA: A Cohort Study.

Roberta Gagliardini, Arturo Ciccullo, Alberto Borghetti, Franco Maggiolo, Dario Bartolozzi, Vanni Borghi, Monica Pecorari, Antonio Di Biagio, Anna Paola Callegaro, Bianca Bruzzone and 7 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 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

17 authors at 8 institutions in 1 country.

Roberta GagliardiniInfectious Diseases Unit, AOU Senese, Siena, Italy.ORCID 0000-0002-6351-2623
Arturo CicculloInstitute of Infectious Diseases, Catholic University of Sacred Heart, Rome, Italy.
Alberto BorghettiInstitute of Infectious Diseases, Catholic University of Sacred Heart, Rome, Italy.
Franco MaggioloDivision of Infectious Diseases, ASST Papa Giovanni XXIII, Bergamo, Italy.
Dario BartolozziClinic of Infectious and Tropical Diseases, Azienda Ospedaliera Universitaria Careggi, Firenze, Italy.
Vanni BorghiClinica Malattie Infettive e Tropicali, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Monica PecorariMicrobiology and Virology Unit, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Antonio Di BiagioInfectious Diseases, IRCCS AOU San Martino-IST, Genova, Italy.
Anna Paola CallegaroMicrobiology and Virology Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.
Bianca BruzzoneHygiene Unit, IRCCS AOU San Martino-IST, Genova, Italy.
Francesco SaladiniDepartment of Medical Biotechnologies, University of Siena, Siena, Italy.
Stefania PaolucciVirologia Molecolare, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Renato MaseratiInfectious Diseases Clinic, S. Matteo Hospital, Pavia, Italy.
Maurizio ZazziDepartment of Medical Biotechnologies, University of Siena, Siena, Italy.
Simona Di GiambenedettoInstitute of Infectious Diseases, Catholic University of Sacred Heart, Rome, Italy.
Andrea De LucaInfectious Diseases Unit, AOU Senese, Siena, Italy.
ARCA Study Group
University of Siena · ITOspedale Papa Giovanni XXIII · ITOspedale Policlinico San Martino · ITUniversità Cattolica del Sacro Cuore · ITAzienda Ospedaliero-Universitaria di Modena · ITPoliclinico San Matteo Fondazione · ITAzienda Ospedaliera Universitaria Senese · ITAzienda Ospedaliero-Universitaria Careggi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDual therapy (DT) with boosted protease inhibitors (bPIs) plus lamivudine has been shown to be superior to bPI monotherapy in virologically suppressed patients despite previous selection of the lamivudine resistance M184V mutation. We compared the virological efficacy of lamivudine-based DT in patients with and without a history of M184V detection.

methodsWe retrospectively analyzed patients with HIV-RNA ≤50 copies/mL switching to DT with at least 1 previous resistance genotype in the ARCA database. Time to virological failure (VF; HIV-RNA ≥200 copies/mL or 2 consecutive HIV-RNA >50 copies/mL) and to treatment discontinuation (TD) was analyzed by survival analysis.

resultsFour hundred thirty-six patients switching to lamivudine plus bPIs (70%) or integrase inhibitors (30%) were included. Patients with M184V (n = 87) were older, had lower nadir CD4+ cell count, longer duration of antiretroviral therapy and of virologic suppression, and higher rate of hepatitis C virus infection compared with patients without M184V. The 3-year probability of remaining free from VF was 91.9% (95% confidence interval [CI], 86.6-97.2) without M184V and 87.8% (95% CI, 78.4-97.2) with M184V (

conclusionsPrevious selection of M184V did not increase the risk of VF or TD with lamivudine-based DT but was associated with a higher probability of viral blips.

Indexed as

dual therapyintegrase inhibitorslamivudineM184VNRTI mutations

Identifiers

PMID29977967
PMCPMC6016422
OpenAlexW2808227723

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.