Evidence map›Paper›PMID 38331373›Full record

ArticleAnalytical biochemistry2024

Single-tube four-target lateral flow assay detects human papillomavirus types associated with majority of cervical cancers.

Maria Barra, Megan Chang, Mila P Salcedo, Kathleen Schmeler, Michael Scheurer, Mauricio Maza, Leticia Lopez, Karla Alfaro, Rebecca Richards-Kortum

Open access · greenAbstract read
In one paragraph

Article in Analytical biochemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

6 citing papers in PubMed, 6 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

9 authors at 3 institutions in 1 country.

Maria BarraDepartment of Bioengineering, Rice University, Houston, TX, USA.
Megan ChangDepartment of Bioengineering, Rice University, Houston, TX, USA.
Mila P SalcedoDepartment of Gynecologic Oncology & Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Kathleen SchmelerDepartment of Gynecologic Oncology & Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Michael ScheurerDepartment of Pediatrics Hematology/Oncology, Baylor College of Medicine, Houston, TX, USA.
Mauricio MazaBasic Health International, San Salvador, El Salvador.
Leticia LopezBasic Health International, San Salvador, El Salvador.
Karla AlfaroBasic Health International, San Salvador, El Salvador.
Rebecca Richards-KortumDepartment of Bioengineering, Rice University, Houston, TX, USA. Electronic address: rkortum@rice.edu.
Rice University · USThe University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · US

Funding

High Resolution Imaging & HPV Oncoprotein Detection for Global Prevention of Cervical CancerR01CA186132 · NCI · RICE UNIVERSITY · PI RICHARDS-KORTUM, REBECCA R. · 2014 to 2018
$3.1M
NCI NIH HHS R01 CA186132
6 · The paper itself

Abstract

Isothermal nucleic acid amplification methods have many advantages for use at the point of care. However, there is a lack of multiplexed isothermal amplification tests to detect multiple targets in a single reaction, which would be valuable for many diseases, such as infection with high-risk human papillomavirus (hrHPV). In this study, we developed a multiplexed loop-mediated isothermal amplification (LAMP) reaction to detect the three most common hrHPV types that cause cervical cancer (HPV16, HPV18, and HPV45) and a cellular control for sample adequacy. First, we characterized the assay limit of detection (LOD) in a real-time reaction with fluorescence readout; after 30 min of amplification the LOD was 100, 10, and 10 copies/reaction of HPV16, HPV18, and HPV45, respectively, and 0.1 ng/reaction of human genomic DNA (gDNA). Next, we implemented the assay on lateral flow strips, and the LOD was maintained for HPV16 and HPV18, but increased to 100 copies/reaction for HPV45 and to 1 ng/reaction for gDNA. Lastly, we used the LAMP test to evaluate total nucleic acid extracted from 38 clinical samples; compared to qPCR, the LAMP test had 89% sensitivity and 95% specificity. When integrated with sample preparation, this multiplexed LAMP assay could be useful for point-of-care testing.

Indexed as

Human papillomavirus 18Papillomavirus InfectionsUterine Cervical NeoplasmsDNA, ViralFemaleHuman papillomavirus 16Human Papillomavirus VirusesHumansNucleic Acid Amplification TechniquesPapillomaviridaeSensitivity and SpecificityDNA, ViralHPVLateral flow assayLoop-mediated isothermal amplificationMultiplex

Identifiers

PMID38331373
PMCPMC11899860
OpenAlexW4391730821

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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.