Evidence map›Paper›PMID 37616294›Full record

ArticlePloS one2023

Genetic and antiretroviral drug resistance mutations analysis of reverse transcriptase and protease gene from Pakistani people living with HIV-1.

Dilsha Siddiqui, Uzma Badar, Mahnoor Javaid, Nida Farooqui, Sharaf Ali Shah, Ayesha Iftikhar, Faisal Sultan, Fatima Mir, Sofia Furqan, Syed Faisal Mahmood and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
2.5field-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.

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, 2 syntheses or guidelines pooled it, 13 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

11 authors at 5 institutions in 2 countries.

Dilsha SiddiquiDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Uzma BadarDepartment of Genetics, University of Karachi, Karachi, Pakistan.
Mahnoor JavaidBridge Consultants Foundation, Karachi, Pakistan.
Nida FarooquiDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Sharaf Ali ShahBridge Consultants Foundation, Karachi, Pakistan.
Ayesha IftikharShaukat Khanum Memorial Hospital and Research Centre, Lahore, Pakistan.
Faisal SultanShaukat Khanum Memorial Hospital and Research Centre, Lahore, Pakistan.
Fatima MirDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Sofia FurqanNational AIDS Control Program, Ministry of Health, Islamabad, Pakistan.
Syed Faisal MahmoodDepartment of Medicine, Aga Khan University, Karachi, Pakistan.
Syed Hani AbidiDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.ORCID 0000-0001-9497-0902
Aga Khan University · PKBridge Consultants Foundation · PKShaukat Khanum Memorial Cancer Hospital and Research Center · PKNational Institute of Health · PKUniversity of Karachi · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntiretroviral therapy (ART) effectiveness is compromised by the emergence of HIV drug resistance mutations (DRM) and can lead to the failure of ART. Apart from intrinsic viral factors, non-compliance with drugs and/or the use of sub-optimum therapy can lead to the emergence of DRMs. In Pakistan HIV currently exists as a concentrated epidemic, however, ART coverage is very low, and drug adherence is poor. ART is selected assuming without baseline genotyping. Pakistan has recently seen a rise in treatment failures, but the country's actual burden of DRM is still unknown. In this study, we perform the genetic and drug resistance analysis of the pol gene from Pakistani HIV-positive ART-naïve and ART-experienced individuals.

methodsIn this study, HIV-1 pol was sequenced from 146 HIV-1 positive individuals, divided into ART-naïve (n = 37) and ART-experienced (n = 109). The sequences were also used to determine HIV-1 subtypes, the prevalence of DRM, and pol genetic variability.

resultsDRM analysis identified numerous DRMs against reverse transcriptase inhibitors in both ART-naïve and ART-experienced groups, including a few that are classified as rare. Additionally, the ART-experienced group showed mutations associated with resistance to protease inhibitors. Genetic analysis showed negative selection pressure in both groups, but a higher rate of evolution in the ART-naïve group.

conclusionHigh prevalence of DRMs, especially against previous first-line treatment in ART- naïve and the accumulation of DRMs in ART-experienced groups is concerning and warrants that a more extensive DRM survey be carried out to inform first-line and second-line ART regimen recommendations.

Indexed as

Anti-Retroviral AgentsDrug Resistance, Multiple, ViralGenes, polHIV-1HIV InfectionsHIV SeropositivityHumansPeptide HydrolasesRNA-Directed DNA PolymeraseSouth Asian PeopleAnti-Retroviral AgentsPeptide HydrolasesRNA-Directed DNA Polymerase

Identifiers

PMID37616294
PMCPMC10449192
OpenAlexW4386127372

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Registered trials

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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.