Evidence map›Paper›PMID 35544100›Full record

SynthesisThe Lancet. Microbe2022

Public availability of HIV-1 drug resistance sequence and treatment data: a systematic review.

Soo-Yon Rhee, Seble G Kassaye, Michael R Jordan, Vinie Kouamou, David Katzenstein, Robert W Shafer

Abstract readSystematic Review
In one paragraph

Synthesis in The Lancet. Microbe, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Kinetic coevolutionary models predict the temporal emergence of HIV-1 resistance mutations under drug selection pressure.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Current Perspectives in Antiviral Research.International journal of molecular sciences · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Review
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

6 authors.

Soo-Yon RheeDepartment of Medicine, Stanford University, Stanford, CA, USA. Electronic address: syrhee@stanford.edu.
Seble G KassayeDepartment of Medicine, Georgetown University, Washington, DC, USA.
Michael R JordanLevy Center for Integrated Management of Antimicrobial Resistance, Tufts University, Boston, MA, USA; Division of Geographic Medicine and Infectious Diseases, Tufts Medical Center, Boston, MA, USA.
Vinie KouamouUnit of Medicine, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
David KatzensteinDepartment of Molecular Biology, Biomedical Research and Training Institute, Harare, Zimbabwe.
Robert W ShaferDepartment of Medicine, Stanford University, Stanford, CA, USA.

Funding

HIV Drug Resistance DatabaseR24AI136618 · NIAID · STANFORD UNIVERSITY · PI ROBERT William SHAFER · 2018 to 2026
$7.3M
Advanced Training in Community Based Research; training in Bio-informatics, Drug Resistance and PathogenesisD43TW011326 · FIC · BIOMEDICAL RESEARCH & TRAINING INSTITUTE · PI MUNYATI, SHUNGU · 2020 to 2024
$1.6M
FIC NIH HHS D43 TW011326NIAID NIH HHS R24 AI136618
6 · The paper itself

Abstract

HIV-1 pol sequences from antiretroviral therapy (ART)-naive and ART-experienced people living with HIV-1 are fundamental to understanding the genetic correlates and epidemiology of HIV-1 drug resistance (HIVDR). To assess the public availability of HIV-1 pol sequences and ART histories of the individuals from whom sequenced viruses were obtained, we performed a systematic review of PubMed and GenBank for HIVDR studies published between 2010 and 2019 that reported HIV-1 pol sequences. 934 studies met inclusion criteria, including 461 studies of ART-naive adults, 407 of ART-experienced adults, and 66 of ART-naive and ART-experienced children. Sequences were available for 317 (68·8%) studies of ART-naive individuals, 190 (46·7%) of ART-experienced individuals, and 45 (68·2%) of children. Among ART-experienced individuals, sequences plus linked ART histories were available for 82 (20·1%) studies. Sequences were available for 21 (29·2%) of 72 clinical trials. Among journals publishing more than ten studies, the proportion with available sequences ranged from 8·3% to 86·9%. Strengthened implementation of data sharing policies is required to increase the number of studies with available HIVDR data to support the enterprise of global ART in the face of emerging HIVDR.

Indexed as

Anti-HIV AgentsHIV-1HIV InfectionsHIV SeropositivityAdultChildDrug Resistance, ViralHumansMutationViral LoadAnti-HIV Agents

Identifiers

PMID35544100
PMCPMC9095989

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.