Evidence map›Paper›PMID 34848705›Full record

ArticleNature communications2021

Paper microfluidic implementation of loop mediated isothermal amplification for early diagnosis of hepatitis C virus.

Weronika Witkowska McConnell, Chris Davis, Suleman R Sabir, Alice Garrett, Amanda Bradley-Stewart, Pawel Jajesniak, Julien Reboud, Gaolian Xu, Zhugen Yang, Rory Gunson and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 78 citations in OpenAlex.

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  12. Current advances in Hepatitis C diagnostics.Journal of biological engineering · 2024
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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

12 authors at 3 institutions in 1 country.

Weronika Witkowska McConnellMRC-University of Glasgow, Centre for Virus Research, University of Glasgow, Glasgow, UK.ORCID 0000-0002-8925-1791
Chris DavisMRC-University of Glasgow, Centre for Virus Research, University of Glasgow, Glasgow, UK.
Suleman R SabirMRC-University of Glasgow, Centre for Virus Research, University of Glasgow, Glasgow, UK.
Alice GarrettDivision of Biomedical Engineering, James Watt School of Engineering, University of Glasgow, Glasgow, UK.
Amanda Bradley-StewartWest of Scotland Specialist Virology Centre, New Lister Building, Glasgow Royal Infirmary, Glasgow, UK.
Pawel JajesniakDivision of Biomedical Engineering, James Watt School of Engineering, University of Glasgow, Glasgow, UK.
Julien ReboudDivision of Biomedical Engineering, James Watt School of Engineering, University of Glasgow, Glasgow, UK.ORCID 0000-0002-6879-8405
Gaolian XuDivision of Biomedical Engineering, James Watt School of Engineering, University of Glasgow, Glasgow, UK.
Zhugen YangDivision of Biomedical Engineering, James Watt School of Engineering, University of Glasgow, Glasgow, UK.ORCID 0000-0003-4183-8160
Rory GunsonWest of Scotland Specialist Virology Centre, New Lister Building, Glasgow Royal Infirmary, Glasgow, UK.
Emma C ThomsonMRC-University of Glasgow, Centre for Virus Research, University of Glasgow, Glasgow, UK. emma.thomson@glasgow.ac.uk.ORCID 0000-0003-1482-0889
Jonathan M CooperDivision of Biomedical Engineering, James Watt School of Engineering, University of Glasgow, Glasgow, UK. jon.cooper@glasgow.ac.uk.ORCID 0000-0002-2358-1050
University of Glasgow · GBMRC University of Glasgow Centre for Virus Research · GBGlasgow Royal Infirmary · GB

Funding

Medical Research Council G0801566Medical Research Council G0901213-92157Medical Research Council MC_PC_16045Medical Research Council MC_UU_12014/1Medical Research Council MR/K013491/1Wellcome TrustWellcome Trust (Wellcome) 102789/Z/13/A
6 · The paper itself

Abstract

The early diagnosis of active hepatitis C virus (HCV) infection remains a significant barrier to the treatment of the disease and to preventing the associated significant morbidity and mortality seen, worldwide. Current testing is delayed due to the high cost, long turnaround times and high expertise needed in centralised diagnostic laboratories. Here we demonstrate a user-friendly, low-cost pan-genotypic assay, based upon reverse transcriptase loop mediated isothermal amplification (RT-LAMP). We developed a prototype device for point-of-care use, comprising a LAMP amplification chamber and lateral flow nucleic acid detection strips, giving a visually-read, user-friendly result in <40 min. The developed assay fulfils the current guidelines recommended by World Health Organisation and is manufactured at minimal cost using simple, portable equipment. Further development of the diagnostic test will facilitate linkage between disease diagnosis and treatment, greatly improving patient care pathways and reducing loss to follow-up, so assisting in the global elimination strategy.

Indexed as

Biomedical EngineeringBlood Urea NitrogenDiagnostic Tests, RoutineEarly DiagnosisGenotypeHepacivirusHepatitis CHumansLaboratoriesMicrofluidicsMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesPoint-of-Care SystemsViral LoadWorld Health Organization

Identifiers

PMID34848705
PMCPMC8632961
OpenAlexW3217176139

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.