Evidence map›Paper›PMID 29424786›Full record

Trial reportAIDS (London, England)2018

No neurocognitive advantage for immediate antiretroviral treatment in adults with greater than 500 CD4+ T-cell counts.

Edwina J Wright, Birgit Grund, Kevin R Robertson, Lucette Cysique, Bruce J Brew, Gary L Collins, Mollie Poehlman-Roediger, Michael J Vjecha, Augusto César Penalva de Oliveira, Barbara Standridge and 11 more

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in AIDS (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Article
  7. Review
  8. Is HIV Brain Disease Preventable?Neurology(R) neuroimmunology & neuroinflammation · 2022
    Article
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  12. Review
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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

21 authors at 14 institutions in 8 countries.

Edwina J WrightDepartment of Infectious Diseases Alfred Health, Monash University, Burnet Institute, The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Birgit GrundSchool of Statistics, University of Minnesota, Minneapolis, Minnesota.
Kevin R RobertsonDepartment of Neurology, University of North Carolina, North Carolina, USA.
Lucette CysiqueNeurosciences Research Australia, St. Vincent's Hospital Sydney, Applied Medical Research Centre.
Bruce J BrewNeurosciences Program, Peter Duncan Neurosciences Unit, St Vincent's Centre for Applied Medical Research, University of New South Wales, Sydney, Australia.
Gary L CollinsDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
Mollie Poehlman-RoedigerDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
Michael J VjechaInstitute for Clinical Research, Inc, Washington, DC, USA.
Augusto César Penalva de OliveiraInstituto Emilio Ribas, Sao Paulo, Brazil.
Barbara StandridgeVeterans Affairs Medical Center, Washington DC, USA.
Cate CareyKirby Institute, University of New South Wales, Sydney, Australia.
Anchalee AvihingsanonHIV-NAT Thai Red Cross AIDS Research Centre and Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Eric FlorenceDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Jens D LundgrenCHIP, Department of Infectious Diseases, Rigshospitalet, University of Copenhagen, Denmark.
Alejandro Arenas-PintoMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, University College London, London, UK.
Nicolas J MuellerDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zürich, Switzerland.
Alan WinstonDivision of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Moses S NsubugaPeople in Need Agency (PINA), Uganda.
Luxshimi LalBurnet Institute, Melbourne, Australia.
Richard W PriceDepartment of Neurology, University of California San Francisco, San Francisco, California, USA.
INSIGHT START Neurology Substudy Group
University of Minnesota · USUNSW Sydney · AUBurnet Institute · AUHIV Netherlands Australia Thailand Research Collaboration · THImperial College London · GBInstituto de Infectologia Emílio Ribas · BRInstituut voor Tropische Geneeskunde · BENeuroscience Research Australia · AUPeter Doherty Institute · AURigshospitalet · DKUniversity College London · GBUniversity Hospital of Zurich · CHUniversity of California, San Francisco · USVeterans Health Administration · US

Funding

International Network for Strategic Initiatives in Global HIV Trials (INSIGHT)UM1AI068641 · NIAID · UNIVERSITY OF MINNESOTA · PI NEATON, JAMES DENNIS · 2011 to 2014
$83.5M
International Network for Strategic Initiatives in Global HIV Trials (INSIGHT): STARTUM1AI120197 · NIAID · UNIVERSITY OF MINNESOTA · PI NEATON, JAMES DENNIS · 2015 to 2017
$65.1M
Medical Research Council MC_UU_12023/23NIAID NIH HHS UM1 AI068641NIAID NIH HHS UM1 AI120197
6 · The paper itself

Abstract

objectiveTo compare the effect of immediate versus deferred antiretroviral treatment (ART) on neuropsychological test performance in treatment-naive HIV-positive adults with more than 500 CD4 cells/μl.

designRandomized trial.

methodsThe START parent study randomized participants to commence immediate versus deferred ART until CD4 less than 350 cells/μl. The START Neurology substudy used eight neuropsychological tests, at baseline, months 4, 8, 12 and annually, to compare groups for changes in test performance. Test results were internally standardized to z-scores. The primary outcome was the average of the eight test z-scores (QNPZ-8). Mean changes in QNPZ-8 from baseline were compared by intent-to-treat using longitudinal mixed models. Changes from baseline to specific time points were compared using ANCOVA models.

resultsThe 592 participants had a median age of 34 years; median baseline CD4 count was 629 cells/μl; the mean follow-up was 3.4 years. ART was used for 94 and 32% of accrued person-years in the immediate and deferred groups, respectively. There was no difference between the immediate and deferred ART groups in QNPZ-8 change through follow-up [-0.018 (95% CI -0.062 to 0.027, P = 0.44)], or at any visit. However, QNPZ-8 scores increased in both arms during the first year, by 0.22 and 0.24, respectively (P < 0.001 for increase from baseline).

conclusionWe observed substantial improvement in neurocognitive test performance during the first year in both study arms, underlining the importance of using a control group in studies assessing neurocognitive performance over time. Immediate ART neither benefitted nor harmed neurocognitive performance in individuals with CD4 cell counts above 500 cells/μl.

Indexed as

Secondary PreventionAdultAIDS Dementia ComplexAnti-Retroviral AgentsCD4 Lymphocyte CountFemaleHIV InfectionsHumansLongitudinal StudiesMaleTreatment OutcomeAnti-Retroviral Agents

Identifiers

PMID29424786
PMCPMC5920693
OpenAlexW2791108978

What OpenQuestion holds

Textmetadata
LicenceTDM
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.