Evidence map›Paper›PMID 30939607›Full record

ArticleRevista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia2019

Assessment of Metalloproteinase Matrix 9 (MMP9) Gene Polymorphisms Risk Factors for Pelvic Organ Prolapse in the Brazilian Population.

Frederico Rezende Ghersel, Ricardo Peres Souto, Ester Wilma Pacheco Gonzales, Denise Souza Paulo, César Eduardo Fernandes, Emerson Oliveira

Open access · diamondAbstract read
In one paragraph

Article in Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Women with pelvic organ prolapse and fibulin-5 rs12589592 polymorphism.Revista da Associacao Medica Brasileira (1992) · 2024
    Article
  4. 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

6 authors at 1 institution in 1 country.

Frederico Rezende GherselDepartment of Urogynecology and Vaginal Surgery, Discipline of Gynecology, Faculdade de Medicina do ABC, Santo André, SP, Brazil.ORCID 0000-0002-0152-6763
Ricardo Peres SoutoDepartment of Urogynecology and Vaginal Surgery, Discipline of Gynecology, Faculdade de Medicina do ABC, Santo André, SP, Brazil.
Ester Wilma Pacheco GonzalesDepartment of Urogynecology and Vaginal Surgery, Discipline of Gynecology, Faculdade de Medicina do ABC, Santo André, SP, Brazil.
Denise Souza PauloDepartment of Urogynecology and Vaginal Surgery, Discipline of Gynecology, Faculdade de Medicina do ABC, Santo André, SP, Brazil.
César Eduardo FernandesDepartment of Urogynecology and Vaginal Surgery, Discipline of Gynecology, Faculdade de Medicina do ABC, Santo André, SP, Brazil.
Emerson OliveiraDepartment of Urogynecology and Vaginal Surgery, Discipline of Gynecology, Faculdade de Medicina do ABC, Santo André, SP, Brazil.
Faculdade de Medicina do ABC · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the

methodsCohort study with 86 women with symptomatic POP (cases), and 158 women without a prior or current diagnosis of this disorder (controls). The groups were analyzed for the presence of

resultsThere were no differences between the cases and controls even when we grouped the mutant homozygous and heterozygous genotypes. The analysis of patients with a complete absence of POP versus patients with total POP also showed no statistically significant differences. Age and home birth were found to be independent risk factors for POP.

conclusionsThere were no statistically significant differences in the

Indexed as

AgedAge DistributionCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHome ChildbirthHumansMatrix Metalloproteinase 9Middle AgedParityPelvic Organ ProlapsePolymorphism, GeneticRisk FactorsMatrix Metalloproteinase 9MMP9 protein, human

Identifiers

PMID30939607
PMCPMC10309288
OpenAlexW2926873640

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.