Evidence map›Paper›PMID 29595649›Full record

ArticleMedicine2018

Next-generation sequencing provides an added value in determining drug resistance and viral tropism in Cameroonian HIV-1 vertically infected children.

Joseph Fokam, Maria C Bellocchi, Daniele Armenia, Aubin J Nanfack, Luca Carioti, Fabio Continenza, Desire Takou, Edith S Temgoua, Charlotte Tangimpundu, Judith N Torimiro and 8 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 16 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

18 authors at 5 institutions in 4 countries.

Joseph FokamChantal Biya International Reference Centre for research on HIV/AIDS Prevention and Management, Yaounde, Cameroon University of Rome Tor Vergata, Rome, Italy University of Yaounde I National HIV Drug Resistance Prevention and Surveillance Working Group, Yaounde, Cameroon New York University School of Medicine, New York, NY National Institute for Infectious Diseases Lazzaro Spallanzani-IRCCS, Rome, Italy Mother-Child Center, Chantal BIYA Foundation, Yaounde University of Bamenda, Bamenda, Cameroon National Research Council UNESCO Board of Multidisciplinary Biotechnology, Rome, Italy.
Maria C Bellocchi
Daniele Armenia
Aubin J Nanfack
Luca Carioti
Fabio Continenza
Desire Takou
Edith S Temgoua
Charlotte Tangimpundu
Judith N Torimiro
Paul N Koki
Charles N Fokunang
Giulia Cappelli
Alexis Ndjolo
Vittorio Colizzi
Francesca Ceccherini-Silberstein
Carlo-Federico Perno
Maria M Santoro
University of Rome Tor Vergata · ITCentre International De Reference Chantal Biya · CMUniversité de Yaoundé I · CMIstituti di Ricovero e Cura a Carattere Scientifico · ITNational Radiation Protection Agency of Cameroon · CM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With limited and low-genetic barrier drugs used for the prevention of mother-to-child transmission (PMTCT) of HIV in sub-Saharan Africa, vertically transmitted HIV-1 drug-resistance (HIVDR) is concerning and might prompt optimal pediatric strategies.The aim of this study was to ascertain HIVDR and viral-tropism in majority and minority populations among Cameroonian vertically infected children.A comparative analysis among 18 HIV-infected children (7 from PMTCT-exposed mothers and 11 from mothers without PMTCT-exposure) was performed. HIVDR and HIV-1 co-receptor usage was evaluated by analyzing sequences obtained by both Sanger sequencing and ultra-deep 454-pyrosequencing (UDPS), set at 1% threshold.Overall, median (interquartile range) age, viremia, and CD4 count were 6 (4-10) years, 5.5 (4.9-6.0) log10 copies/mL, and 526 (282-645) cells/mm, respectively. All children had wild-type viruses through both Sanger sequencing and UDPS, except for 1 PMTCT-exposed infant harboring minority K103N (8.31%), born to a mother exposed to AZT+3TC+NVP. X4-tropic viruses were found in 5 of 15 (33.3%) children (including 2 cases detected only by UDPS). Rate of X4-tropic viruses was 0% (0/6) below 5 years (also as minority species), and became relatively high above 5 years (55.6% [5/9], P = .040. X4-tropic viruses were higher with CD4 ≤15% (4/9 [44.4%]) versus CD4 >15% (1/6 [16.7%], P = .580); similarly for CD4 ≤200 (3/4 [75%]) versus CD4 >200 (2/11 [18.2%] cells/mm, P = .077.NGS has the ability of excluding NRTI- and NNRTI-mutations as minority species in all but 1 children, thus supporting the safe use of these drug-classes in those without such mutations, henceforth sparing ritonavir-boosted protease inhibitors or integrase inhibitors for the few remaining cases. In children under five years, X4-tropic variants would be rare, suggesting vertical-transmission with CCR5-tropic viruses and possible maraviroc usage at younger ages.

Indexed as

Anti-HIV AgentsCameroonCD4 Lymphocyte CountChildChild, PreschoolDrug Resistance, ViralFemaleHigh-Throughput Nucleotide SequencingHIV-1HIV InfectionsHumansInfectious Disease Transmission, VerticalMaleRNA, ViralViral TropismAnti-HIV AgentsRNA, Viral

Identifiers

PMID29595649
PMCPMC5895385
OpenAlexW2794463326

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.