Evidence map›Paper›PMID 27625109›Full record

ArticleHIV medicine2017

Higher rates of triple-class virological failure in perinatally HIV-infected teenagers compared with heterosexually infected young adults in Europe.

A Judd, R Lodwick, A Noguera-Julian, D M Gibb, K Butler, D Costagliola, C Sabin, A van Sighem, B Ledergerber, C Torti and 23 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in HIV medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
4.7field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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  20. Using Observational Data to Inform HIV Policy Change for Children and Youth.Journal of acquired immune deficiency syndromes (1999) · 2018
    Observational
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

33 authors at 20 institutions in 13 countries.

A JuddMRC Clinical Trials Unit, University College London, London, UK.ORCID 0000-0003-3176-5295
R LodwickDepartment of Infection and Population Health, University College London, London, UK.
A Noguera-JulianInstitut de Recerca Pediàtrica Hospital Sant Joan de Déu, Barcelona, Spain.
D M GibbMRC Clinical Trials Unit, University College London, London, UK.
K ButlerDepartment of Infectious Diseases and Immunology, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.
D CostagliolaINSERM, UPMC Univ Paris 06, Institut Pierre Louis d'épidémiologie et de Santé Publique (IPLESP UMRS 1136), Sorbonne Universités, Paris, France.
C SabinDepartment of Infection and Population Health, University College London, London, UK.
A van SighemStichting HIV Monitoring, Amsterdam, The Netherlands.
B LedergerberDivision of Infectious Diseases and Hospital Epidemiology, University of Zurich, Zurich, Switzerland.
C TortiUnit of Infectious and Tropical Diseases, Department of Medical and Surgical Sciences, University "Magna Graecia", Catanzaro, Italy.
A MocroftDepartment of Infection and Population Health, University College London, London, UK.
D PodzamczerHIV and STD Unit, Infectious Disease Service, Hospital Universitari de Bellvitge. L'Hospitalet, Barcelona, Spain.
M DorrucciIstituto Superiore di Sanità, Rome, Italy.
S De WitDépartement of Infectious Diseases, Centre Hospitalier Saint-Pierre, Université Libre de Bruxelles, Brussels, Belgium.
N ObelDepartment of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
F DabisINSERM U1219 - Centre Inserm Bordeaux Population Health, Université de Bordeaux, Bordeaux, France.
A Cozzi-LepriDepartment of Infection and Population Health, University College London, London, UK.
F GarcíaClinical Microbiology Department, Complejo Hospitalario Universitario Granada, Instituto de Investigación Biosanitaria ibs.Granada, Granada, Spain.
N H BrockmeyerDepartment of Dermatology, Venerology and Allergology, Center for Sexual Health and Medicine, St. Josef Hospital, Ruhr-Universität Bochum, Bochum, Germany.
J WarszawskiINSERM CESP U1018, AP-HP Public Health Department, Université Paris-Sud, Université Paris-Saclay, Le Kremlin-Bicêtre Paris, France.
M I Gonzalez-TomeHIV and Paeds Infectious Diseases Department, Hospital 12 de Octubre, Madrid, Spain.
C MussiniInfectious Diseases Clinics, University Hospital, Modena, Italy.
G TouloumiDepartment Hygiene, Epidemiology & Medical Statistics, Medical School, National & Kapodistrian University of Athens, Athens, Greece.
R ZangerleMedical University Innsbruck, Innsbruck, Austria.
J GhosnEA 7327, Faculté de Médecine site Necker, Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
A CastagnaSan Raffaele Scientific Institute, Vita-SaLute University, Milan, Italy.
G FätkenheuerDepartment I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
C StephanSecond Medical Department, Infectious Diseases Unit, Goethe-University Hospital, Frankfurt, Germany.
L MeyerINSERM CESP U1018, Université Paris-Sud, Université Paris-Saclay, Paris, France.
M A CampbellCentre for Health and Infectious Disease Research, University of Copenhagen, Copenhagen, Denmark.
G CheneINSERM U1219 - Centre Inserm Bordeaux Population Health, Université de Bordeaux, Bordeaux, France.
A PhillipsDepartment of Infection and Population Health, University College London, London, UK.
Pursuing Later Treatment Options II (PLATO II) Project Team for the Collaboration of Observational HIV Epidemiological Research Europe (COHERE) in EuroCoord
University College London · GBMRC Clinical Trials Unit at UCL · GBUniversité de Bordeaux · FRUniversité Paris-Sud · FRBellvitge University Hospital · ESChildren's Health Ireland at Crumlin · IECopenhagen University Hospital · DKDélégation Paris 5 · FRGoethe University Frankfurt · DEHospital Sant Joan de Déu Barcelona · ESInnsbruck Medical University · ATInserm · FRInstituto de Investigación Biosanitaria de Granada · ESIstituto Superiore di Sanità · ITMagna Graecia University · ITNational and Kapodistrian University of Athens · GRResearch Institute Hospital 12 de Octubre · ESStichting HIV Monitoring · NLSt. Josef-Hospital · DEUniversité Libre de Bruxelles · BE

Funding

Medical Research Council G0700832Medical Research Council MC_UU_12023/15Medical Research Council MC_UU_12023/17Medical Research Council MC_UU_12023/26Medical Research Council MR/M004236/1
6 · The paper itself

Abstract

objectivesThe aim of the study was to determine the time to, and risk factors for, triple-class virological failure (TCVF) across age groups for children and adolescents with perinatally acquired HIV infection and older adolescents and adults with heterosexually acquired HIV infection.

methodsWe analysed individual patient data from cohorts in the Collaboration of Observational HIV Epidemiological Research Europe (COHERE). A total of 5972 participants starting antiretroviral therapy (ART) from 1998, aged < 20 years at the start of ART for those with perinatal infection and 15-29 years for those with heterosexual infection, with ART containing at least two nucleoside reverse transcriptase inhibitors (NRTIs) and a nonnucleoside reverse transcriptase inhibitor (NNRTI) or a boosted protease inhibitor (bPI), were followed from ART initiation until the most recent viral load (VL) measurement. Virological failure of a drug was defined as VL > 500 HIV-1 RNA copies/mL despite ≥ 4 months of use. TCVF was defined as cumulative failure of two NRTIs, an NNRTI and a bPI.

resultsThe median number of weeks between diagnosis and the start of ART was higher in participants with perinatal HIV infection compared with participants with heterosexually acquired HIV infection overall [17 (interquartile range (IQR) 4-111) vs. 8 (IQR 2-38) weeks, respectively], and highest in perinatally infected participants aged 10-14 years [49 (IQR 9-267) weeks]. The cumulative proportion with TCVF 5 years after starting ART was 9.6% [95% confidence interval (CI) 7.0-12.3%] in participants with perinatally acquired infection and 4.7% (95% CI 3.9-5.5%) in participants with heterosexually acquired infection, and highest in perinatally infected participants aged 10-14 years when starting ART (27.7%; 95% CI 13.2-42.1%). Across all participants, significant predictors of TCVF were those with perinatal HIV aged 10-14 years, African origin, pre-ART AIDS, NNRTI-based initial regimens, higher pre-ART viral load and lower pre-ART CD4.

conclusionsThe results suggest a beneficial effect of starting ART before adolescence, and starting young people on boosted PIs, to maximize treatment response during this transitional stage of development.

Indexed as

Drug Resistance, ViralPopulation GroupsAdolescentAdultAnti-Retroviral AgentsChildChild, PreschoolCohort StudiesEuropeFemaleHIV InfectionsHumansInfantMaleTime FactorsTreatment FailureAnti-Retroviral AgentsEuropeperinatal HIV infectionvirological failureyoung people

Identifiers

PMID27625109
PMCPMC5298034
OpenAlexW2521009540

What OpenQuestion holds

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LicenceCC BY
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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.