Evidence map›Paper›PMID 23485767›Full record

ArticleThe Journal of antimicrobial chemotherapy2013

Computational models can predict response to HIV therapy without a genotype and may reduce treatment failure in different resource-limited settings.

A D Revell, D Wang, R Wood, C Morrow, H Tempelman, R L Hamers, G Alvarez-Uria, A Streinu-Cercel, L Ene, A M J Wensing and 6 more

Registry-linked trialOpen access · bronzeAbstract read
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. It is linked to trial NCT02454569 (Vicente Ferrer HIV Cohort Study), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.6field-weighted citation impact, top 10% 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.

NCT02454569 recruitingnot on this map

Vicente Ferrer HIV Cohort Study

Typeobservational_patient_registrySponsorRural Development Trust HospitalRan2009 to 2040Enrolled30,000ConditionsHIV, Tuberculosis, Cryptococcosis, Opportunistic Infections
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 34 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

16 authors at 11 institutions in 7 countries.

A D RevellThe HIV Resistance Response Database Initiative (RDI), London, UK.
D Wang
R Wood
C Morrow
H Tempelman
R L Hamers
G Alvarez-Uria
A Streinu-Cercel
L Ene
A M J Wensing
F DeWolf
M Nelson
J S Montaner
H C Lane
B A Larder
RDI study group
Desmond Tutu HIV Foundation · ZAAIDS Vancouver · CAAmsterdam Institute for Global Health and Development · NLChelsea and Westminster Hospital · GBMedical Trust Hospital · INNational Institute of Allergy and Infectious Diseases · USNational Institute of Research and Development for Biological Sciences · RORight to Care · ZASpitalul Clinic Dr. Victor Babes · ROStichting HIV Monitoring · NLUniversity Medical Center Utrecht · NL

Funding

Pathogenesis and Treatment of HIV InfectionZIAAI000585 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LANE, CLIFFORD · 2009 to 2025
$26.8M
PHS HHS HHSN261200800001E
6 · The paper itself

Abstract

objectivesGenotypic HIV drug-resistance testing is typically 60%-65% predictive of response to combination antiretroviral therapy (ART) and is valuable for guiding treatment changes. Genotyping is unavailable in many resource-limited settings (RLSs). We aimed to develop models that can predict response to ART without a genotype and evaluated their potential as a treatment support tool in RLSs.

methodsRandom forest models were trained to predict the probability of response to ART (≤400 copies HIV RNA/mL) using the following data from 14 891 treatment change episodes (TCEs) after virological failure, from well-resourced countries: viral load and CD4 count prior to treatment change, treatment history, drugs in the new regimen, time to follow-up and follow-up viral load. Models were assessed by cross-validation during development, with an independent set of 800 cases from well-resourced countries, plus 231 cases from Southern Africa, 206 from India and 375 from Romania. The area under the receiver operating characteristic curve (AUC) was the main outcome measure.

resultsThe models achieved an AUC of 0.74-0.81 during cross-validation and 0.76-0.77 with the 800 test TCEs. They achieved AUCs of 0.58-0.65 (Southern Africa), 0.63 (India) and 0.70 (Romania). Models were more accurate for data from the well-resourced countries than for cases from Southern Africa and India (P < 0.001), but not Romania. The models identified alternative, available drug regimens predicted to result in virological response for 94% of virological failures in Southern Africa, 99% of those in India and 93% of those in Romania.

conclusionsWe developed computational models that predict virological response to ART without a genotype with comparable accuracy to genotyping with rule-based interpretation. These models have the potential to help optimize antiretroviral therapy for patients in RLSs where genotyping is not generally available.

Indexed as

AdultAfrica South of the SaharaAnti-HIV AgentsComputer SimulationDatabases, FactualFemaleFollow-Up StudiesHealth ResourcesHIVHIV InfectionsHIV Protease InhibitorsHumansIndiaMaleMiddle AgedModels, StatisticalAnti-HIV AgentsHIV Protease InhibitorsReverse Transcriptase Inhibitorsantiretroviral therapycomputer modelsHIV drug resistancepredictionsresource-limited settings.treatment outcomes

Identifiers

PMID23485767
PMCPMC3654223
OpenAlexW2132471816

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Registered trials

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.