Evidence map›Paper›PMID 35766692›Full record

ArticleRevista da Associacao Medica Brasileira (1992)2022

Polymorphisms rs2010963 and rs833061 of the VEGF gene in polycystic ovary syndrome.

Anna Luiza Silva Almeida Vicente, Alessandra Bernadete Trovó de Marqui, Mariana Kefalas Oliveira Gomes, Alan Vinicius Assunção-Luiz, Marly Aparecida Spadotto Balarin, Sarah Cristina Sato Vaz Tanaka, Elisabete Aparecida Mantovani Rodrigues de Resende, Marco Fábio Prata Lima, Mariangela Torreglosa Ruiz Cintra

Open access · diamondAbstract read
In one paragraph

Article in Revista da Associacao Medica Brasileira (1992), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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.

Anna Luiza Silva Almeida VicenteHospital de Câncer de Barretos - Barretos (SP), Brazil.ORCID http://orcid.org/0000-0003-3902-7772
Alessandra Bernadete Trovó de MarquiUniversidade Federal do Triângulo Mineiro - Uberaba (MG), Brazil.ORCID http://orcid.org/0000-0003-2361-5174
Mariana Kefalas Oliveira GomesUniversidade Federal do Triângulo Mineiro - Uberaba (MG), Brazil.ORCID http://orcid.org/0000-0002-5279-5242
Alan Vinicius Assunção-LuizUniversidade de São Paulo, Faculdade de Medicina de Ribeirão Preto - Ribeirão Preto (SP), Brazil.ORCID http://orcid.org/0000-0003-3644-3981
Marly Aparecida Spadotto BalarinUniversidade Federal do Triângulo Mineiro - Uberaba (MG), Brazil.ORCID http://orcid.org/0000-0002-7535-0609
Sarah Cristina Sato Vaz TanakaUniversidade Federal do Triângulo Mineiro - Uberaba (MG), Brazil.ORCID http://orcid.org/0000-0003-4466-6093
Elisabete Aparecida Mantovani Rodrigues de ResendeUniversidade Federal do Triângulo Mineiro - Uberaba (MG), Brazil.ORCID http://orcid.org/0000-0002-8404-1103
Marco Fábio Prata LimaUniversidade Federal do Triângulo Mineiro - Uberaba (MG), Brazil.ORCID http://orcid.org/0000-0001-7271-6620
Mariangela Torreglosa Ruiz CintraUniversidade Federal do Triângulo Mineiro - Uberaba (MG), Brazil.ORCID http://orcid.org/0000-0002-8223-805X
Universidade Federal do Triângulo Mineiro · BRHospital de Câncer de Barretos · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe polycystic ovary syndrome is the most common endocrine disorder, characterized by the dysregulation of ovarian angiogenesis. This alteration can be related to changes in the activities of the vascular endothelial growth factor (VEGF) gene. Single-nucleotide polymorphisms have been observed in the promoter, intronic, and untranslated regions of the VEGF gene, and several studies have suggested that these polymorphisms may be associated with the risk of polycystic ovary syndrome. This study aimed to investigate the association between rs2010963 and rs833061 polymorphisms and haplotypes of VEGF in the etiology of polycystic ovary syndrome.

methodsA total of 210 women, 102 diagnosed with polycystic ovary syndrome and 108 controls, participated in this study. The genotyping of the samples was performed by PCR-RFLP and real-time PCR for rs2010963 and rs833061 polymorphisms, respectively. The statistical analyses were performed by the chi-square test and logistic regression model.

resultsThe clinical characteristics of the patients showed that 75.8% of the patients did not become pregnant, 36.3% had a family history of polycystic ovary syndrome, 58.6% were obese, and about 60% had clinical characteristics of hyperandrogenism. There were no associations between the distribution of rs2010963 (OR 1.24; 95%CI 0.60-2.57; p=0.56) and rs833061 (OR 0.78; 95%CI 0.32-1.92; p=0.59) in patients and controls.

conclusionsThe patients with polycystic ovary syndrome have similar rates of VEGF polymorphisms rs2010963 and rs833061 on the general population.

Indexed as

Polycystic Ovary SyndromeVascular Endothelial Growth Factor ACase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansPolymorphism, Single NucleotidePregnancyVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID35766692
PMCPMC9575905
OpenAlexW4283688656

What Socratic holds

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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 Socratic graph.