Evidence map›Paper›PMID 39597715›Full record

ArticleMicroorganisms2024

Expanded HPV Genotyping by Single-Tube Nested-Multiplex PCR May Explain HPV-Related Disease Recurrence.

Luiz Ricardo Goulart, Bruna França Matias Colombo, Mayara Ingrid Sousa Lima, Maria Socorro A de Andrade, Juliana São Julião, Adriana Freitas Neves, Silma Regina Pereira

Abstract read
In one paragraph

Article in Microorganisms, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

7 authors.

Luiz Ricardo GoulartInstitute of Biotechnology, Federal University of Uberlândia, Uberlândia 38400-902, MG, Brazil.ORCID 0000-0002-1803-4861
Bruna França Matias ColomboInstitute of Biotechnology, Federal University of Uberlândia, Uberlândia 38400-902, MG, Brazil.
Mayara Ingrid Sousa LimaLaboratory of Genetics and Molecular Biology, Department of Biology, Federal University of Maranhão, São Luís 65085-580, MA, Brazil.ORCID 0000-0002-1033-1984
Maria Socorro A de AndradeHealth Department of the State of Maranhão, São Luís 65000-00, MA, Brazil.
Juliana São JuliãoBioGenetics Tecnologia Molecular Ltda., Uberlândia 38400-446, MG, Brazil.
Adriana Freitas NevesInstitute of Biotechnology, Federal University of Catalão, Catalão 75705-220, GO, Brazil.ORCID 0000-0002-2299-2114
Silma Regina PereiraLaboratory of Genetics and Molecular Biology, Department of Biology, Federal University of Maranhão, São Luís 65085-580, MA, Brazil.ORCID 0000-0003-2974-3687

Funding

Fundação de Amparo à Pesquisa do Estado Minas Gerais (FAPEMIG) CBB-APQ-03613-17Instituto Nacional de Ciência e Tecnologia TeraNóstica (INCT TeraNanogrant /CNPq) 403193/2022-2
6 · The paper itself

Abstract

The role of the human papillomavirus (HPV) in the establishment of cervical cancer has driven studies to find more effective methods of viral detection so that early intervention strategies can be performed. However, the methods still have limitations, especially regarding detecting the different genotypes simultaneously. We have developed a high-throughput system using a single-tube nested-multiplex polymerase chain reaction (NMPCR) for the detection of 40 HPV genotypes using capillary electrophoresis. The NMPCR assay was compared to the Hybrid Capture 2 assay (HC2) with 40 women from the Northeast of Brazil (São Luis, MA), a high endemic region, where the HPV positivity was 75% and 37.5%, respectively. These results were validated by performing a molecular epidemiological study on 5223 Brazilian women undergoing gynecological examinations from 2009 to 2017, who presented with an HPV prevalence of 59%. Multiple infections were found in 62.5% and 58% of the patients from the endemic region and from the Brazilian women population, respectively, mostly presenting high-risk genotypes (90.5% and 60%, respectively). Considering cervical intraepithelial neoplasia and adenocarcinomas, the sensitivity and specificity were 97.5% and 100%, respectively. The NMPCR assay was also capable of identifying viral subtypes in cases of multiple infections, even with low viral loads (10

Indexed as

cervical cancerHPV screeningmolecular diagnosticsmolecular epidemiology

Identifiers

PMID39597715
PMCPMC11596377

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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.