Evidence map›Paper›PMID 24165156›Full record

ArticleVirology journal2013

HIV-1 tropism: a comparison between RNA and proviral DNA in routine clinical samples from Chilean patients.

Pablo Ferrer, Luisa Montecinos, Mario Tello, Rocio Tordecilla, Consuelo Rodríguez, Marcela Ferrés, Carlos M Pérez, Carlos Beltrán, Maria A Guzmán, Alejandro Afani

Abstract readComparative StudyEvaluation Study
In one paragraph

Article in Virology journal, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Pablo FerrerLaboratorio de Medicina Molecular, Hospital Clínico Universidad de Chile, Santiago, Chile. pferrer40@gmail.com.
Luisa Montecinos
Mario Tello
Rocio Tordecilla
Consuelo Rodríguez
Marcela Ferrés
Carlos M Pérez
Carlos Beltrán
Maria A Guzmán
Alejandro Afani

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHIV in Chile has a notification rate of 0.01%. Coreceptor antagonists are a family of antiretroviral drugs that are used with the prior knowledge of patients HIV-1 tropism. Viral RNA-based tropism detection requires a plasma viral load ≥1000 copies/mL, while proviral DNA-based detection can be performed regardless of plasma viral load. This test is useful in patients with low or undetectable viral loads and would benefit with a proper therapy. The aim of this study was to determine the correlation between HIV RNA and proviral genotypic DNA tropism tests.

findingsForty three Chilean patients were examined using population-based V3 sequencing, and a geno2pheno false-positive rate (FPR) cutoff values of 5, 5.75, 10 and 20%. With cutoff 5.75% a concordance of 88.4% in tropism prediction was found after a simultaneous comparison between HIV tropism assessment by RNA and DNA. In total, five discrepancies (11.6%) were found, 3 patients were RNA-R5/DNA-X4 and two were RNA-X4/DNA-R5. Proviral DNA enabled the prediction of tropism in patients with a low or undetectable viral load. For cutoff 5 and 5.75% genotypic testing using proviral DNA showed a similar sensitivity for X4 as RNA. We found that the highest sensitivity for detecting the X4 strain occurred with proviral DNA and cutoff of 10 and 20%. Viral loads were higher among X4 strain carriers than among R5 strain carriers (p < 0.05).

conclusionsA high degree of concordance was found between tropism testing with RNA and testing with proviral DNA. Our results suggest that proviral DNA-based genotypic tropism testing is a useful option for patients with low or undetectable viral load who require a different therapy.

Indexed as

Viral TropismAdolescentAdultAgedChileDNA, ViralFemaleGenotypeGenotyping TechniquesHIV-1HIV InfectionsHumansMaleMiddle AgedRNA, ViralVirologyDNA, ViralRNA, Viral

Identifiers

PMID24165156
PMCPMC4231446

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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.