Evidence map›Paper›PMID 27825316›Full record

Observational studyBMC infectious diseases2016

Prevalence and effect of pre-treatment drug resistance on the virological response to antiretroviral treatment initiated in HIV-infected children - a EuroCoord-CHAIN-EPPICC joint project.

Nicole Ngo-Giang-Huong, Linda Wittkop, Ali Judd, Peter Reiss, Tessa Goetghebuer, Dan Duiculescu, Antoni Noguera-Julian, Magdalena Marczynska, Carlo Giacquinto, Luminita Ene and 17 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in BMC infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

27 authors at 17 institutions in 13 countries.

Nicole Ngo-Giang-HuongIRD UMI 174 - PHPT-Faculty of Associated Medical Sciences, Chiang Mai University, 110, Intrawarorot Road, Sripoom, Muang, Chiang Mai, 50200, Thailand. Nicole.Ngo-Giang-Huong@phpt.org.ORCID 0000-0001-8950-3234
Linda WittkopUniv. Bordeaux, ISPED; INSERM, Centre INSERM U1219; CHU de Bordeaux, Pole de Sante Publique, F-33000, Bordeaux, France.
Ali JuddMedical Research Council Clinical Trials Unit, University College London, London, UK.
Peter ReissAcademic Medical Centre, University of Amsterdam, Amsterdam, Netherlands.
Tessa GoetghebuerHôpital Saint-Pierre, Brussel, Belgium.
Dan Duiculescu"Dr. Victor Babes" Hospital for Infectious and Tropical Diseases, Bucharest, Romania.
Antoni Noguera-JulianSant Joan de Déu Hospital, University of Barcelona, Barcelona, Spain.
Magdalena MarczynskaMedical University of Warsaw, Warsaw, Poland.
Carlo GiacquintoUniversity of Padua, Padua, Italy.
Luminita Ene"Dr. Victor Babes" Hospital for Infectious and Tropical Diseases, Bucharest, Romania.
Jose T RamosUniversity Hospital of Getafe, Madrid, Spain.
Cristina CelleraiLausanne University Hospital, Lausanne, Switzerland.
Thomas KlimkaitUniversity of Basel, Basel, Switzerland.
Benedicte BrichardSaint-Luc, Brussels, Belgium.
Niels ValeriusHvidovre Hospital, University of Copenhagen, Copenhagen, Denmark.
Caroline SabinUniversity College London, London, UK.
Ramon TeiraHospital de Sierrallana, Torrelavega, Spain.
Niels ObelRigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Christoph StephanUniversity Clinic Frankfurt, Frankfurt, Germany.
Stéphane de WitAIDS Reference Center, CHU Saint-Pierre, Brussels, Belgium.
Claire ThorneUniversity College London, Institute of Child Health, London, UK.
Diana GibbMedical Research Council Clinical Trials Unit, London, UK.
Christine SchwimmerBordeaux RCC, INSERM, U897, Bordeaux, France.
Maria Athena CampbellCopenhagen RCC, Rigshospitalet, Copenhagen, Denmark.
Deenan PillayUniversity College London, London, UK.
Marc LallemantIRD UMI 174 - PHPT-Faculty of Associated Medical Sciences, Chiang Mai University, 110, Intrawarorot Road, Sripoom, Muang, Chiang Mai, 50200, Thailand.
EuroCoord-CHAIN-EPPICC joint project study group
University College London · GBCentre Hospitalier Universitaire de Saint-Pierre · BEChiang Mai University · THGoethe University Frankfurt · DEHospital Sant Joan de Déu Barcelona · ESHospital Universitario de Getafe · ESInserm · FRUniversity of Copenhagen · DKUniversity of Padua · ITCliniques Universitaires Saint-Luc · BECopenhagen University Hospital · DKHarvard University · USHospital Sierrallana · ESRigshospitalet · DKSpitalul Clinic Dr. Victor Babes · ROUniversité de Bordeaux · FRUniversity of Basel · CH

Funding

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

Abstract

backgroundFew studies have evaluated the impact of pre-treatment drug resistance (PDR) on response to combination antiretroviral treatment (cART) in children. The objective of this joint EuroCoord-CHAIN-EPPICC/PENTA project was to assess the prevalence of PDR mutations and their association with virological outcome in the first year of cART in children.

methodsHIV-infected children <18 years initiating cART between 1998 and 2008 were included if having at least one genotypic resistance test prior to cART initiation. We used the World Health Organization 2009 resistance mutation list and Stanford algorithm to infer resistance to prescribed drugs. Time to virological failure (VF) was defined as the first of two consecutive HIV-RNA > 500 copies/mL after 6 months cART and was assessed by Cox proportional hazards models. All models were adjusted for baseline demographic, clinical, immunology and virology characteristics and calendar period of cART start and initial cART regimen.

resultsOf 476 children, 88 % were vertically infected. At cART initiation, median (interquartile range) age was 6.6 years (2.1-10.1), CD4 cell count 297 cells/mm

conclusionsPDR was not significantly associated with a higher risk of VF in children in the first year of cART. The risk of VF decreased by 12 % per additional year at treatment initiation which may be due to fading of PDR mutations over time. Lack of appropriate formulations, in particular for the younger age group, may be an important determinant of virological failure.

Indexed as

AdolescentAnti-HIV AgentsCD4 Lymphocyte CountChildChild, PreschoolDrug Resistance, ViralDrug Therapy, CombinationFemaleHIV-1HIV InfectionsHumansInfantKaplan-Meier EstimateMaleMutationReverse Transcriptase InhibitorsAnti-HIV AgentsReverse Transcriptase InhibitorsChildrenFirst-line combination antiretroviral therapyHIVPre-treatment drug resistance mutationsVirological failure

Identifiers

PMID27825316
PMCPMC5101717
OpenAlexW2554194219

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.