Evidence map›Paper›PMID 30167873›Full record

ArticleMedical microbiology and immunology2019

Polymorphisms in the TGFB1 signal peptide influence human papillomavirus infection and development of cervical lesions.

Kleber Paiva Trugilo, Guilherme Cesar Martelossi Cebinelli, Fernanda Costa Brandão Berti, Nádia Calvo Martins Okuyama, Fernando Cezar-Dos-Santos, Michelle Mota Sena, Luis Fernando Lásaro Mangieri, Maria Angelica Ehara Watanabe, Karen Brajão de Oliveira

Abstract read
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In one paragraph

Article in Medical microbiology and immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

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

  1. Pooled it
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  6. Prevalence of HPV and associated factors in a population of women living in southern Brazil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2022
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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.

Kleber Paiva TrugiloDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Guilherme Cesar Martelossi CebinelliDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Fernanda Costa Brandão BertiDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Nádia Calvo Martins OkuyamaDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Fernando Cezar-Dos-SantosDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Michelle Mota SenaDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Luis Fernando Lásaro MangieriDepartment of Gynecology and Obstetrics, Health Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Maria Angelica Ehara WatanabeDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil.
Karen Brajão de OliveiraDepartment of Pathological Science, Biological Science Center, State University of Londrina, Londrina, Paraná, Brazil. karen.brajao@gmail.com.ORCID http://orcid.org/0000-0001-9666-6963

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 470137/2013-4FAEPE/UEL PUBLIC 2016Fundação Araucária - Programa Pesquisa para o SUS 34935.406.36850.19112012
6 · The paper itself

Abstract

The main purpose was to assess the effect of c.29C>T and c.74G>C polymorphisms in the TGFB1 signal peptide on HPV infection and development of cervical lesions. Cervical swabs and blood samples were obtained from 349 outpatient women, along with socio-demographic and sexual behavioral data. The study population was stratified by absence or presence of HPV DNA, as tested by PCR, as well as by lesion grade. TGFB1 signal peptide polymorphisms were genotyped using PCR-restriction fragment length polymorphism. HPV DNA was detected in 172 (49.3%) patients. c.74GC and the combined c.29CC+CT/c.74GC genotype were more frequent in infected patients (35.1 and 15.7%) than in uninfected women (6.2 and 14.7%). Accordingly, these genotypes were associated with a higher risk of HPV infection, with odds ratio and 95% confidence interval of 2.81 and 1.35-5.86 (P = 0.004) for c.74GC and 3.14 and 1.42-6.94 (P = 0.004) for the combined genotype, respectively. High-grade lesions were also 2.48 times more likely to occur in c.29CC patients than in c.29TT patients, with a 95% confidence interval of 1.01-6.08 (P = 0.047). The data demonstrate that c.74G>C and c.29C>T polymorphisms are significantly associated with risk of HPV infection and high-grade squamous intraepithelial lesions, respectively. Thus, TGFB1 signal peptide polymorphisms are potential susceptibility markers.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAgedAged, 80 and overCase-Control StudiesFemaleGenotypeHumansMiddle AgedNeoplasm GradingPapillomavirus InfectionsPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthProtein Sorting SignalsSquamous Intraepithelial Lesions of the CervixProtein Sorting SignalsTGFB1 protein, humanTransforming Growth Factor beta1rs1800470rs1800471Susceptibility markersTGFB1 combined genotype

Identifiers

What OpenQuestion holds

Textmetadata
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.