Evidence map›Paper›PMID 38666947›Full record

ArticleCurrent issues in molecular biology2024

Frequency of Gene Polymorphisms in Admixed Venezuelan Women with Recurrent Pregnancy Loss: Microsomal Epoxy Hydroxylase (rs1051740) and Enos (rs1799983).

María Johanna Peña, Claudia Valentina De Sanctis, Juan Bautista De Sanctis, Jenny Valentina Garmendia

Open access · goldAbstract read
In one paragraph

Article in Current issues in molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 2 countries.

María Johanna PeñaInstitute of Immunology, Faculty of Medicine, Universidad Central de Venezuela, Caracas 1040, Venezuela.
Claudia Valentina De SanctisInstitute of Immunology, Faculty of Medicine, Universidad Central de Venezuela, Caracas 1040, Venezuela.
Juan Bautista De SanctisInstitute of Immunology, Faculty of Medicine, Universidad Central de Venezuela, Caracas 1040, Venezuela.ORCID 0000-0002-5480-4608
Jenny Valentina GarmendiaInstitute of Immunology, Faculty of Medicine, Universidad Central de Venezuela, Caracas 1040, Venezuela.
Central University of Venezuela · VEInstitute of Molecular and Translational Medicine · CZ

Funding

CDCH-UCV PG 09-6599-2006/1
6 · The paper itself

Abstract

Recurrent pregnancy loss (RPL) affects around 2% of women of reproductive age. Primary RPL is defined by ≥2 pregnancy losses and no normal birth delivery. In secondary RPL, the losses are after a normal pregnancy and delivery. Most cases have no clear aetiology, although primary cases are the most complex. Several gene single nucleotide polymorphisms (SNPs) have been associated with RPL. The frequency of some SNPs is increased in women suffering from RLP from Asian or Caucasian races; however, in admixed populations, the information on possible genetic links is scarce and contradictory. This study aimed to assess the frequency of two SNPs present in two different enzymes involved in medical conditions observed during pregnancy. It is a case-control study. Microsomal epoxy hydrolase (mEPH) is involved in detoxifying xenobiotics, is present in the ovaries, and is hormonally regulated. The endothelial nitric oxide synthase (NOS3) that forms nitric is involved in vascular tone. Two SNPs, rs1051740 (mEPH) and rs1799983 (NOS3), were assessed. The study included 50 controls and 63 primary RPL patients. The frequency of mutated alleles in both SNPs was significantly higher in patients (

Indexed as

endothelial nitric oxide synthase (eNOS)microsomal epoxy hydrolase (mEPH)recurrent pregnancy lossrs1051740rs1799983single nucleotide gene polymorphism (SNP)

Identifiers

PMID38666947
PMCPMC11049659
OpenAlexW4394892107

What OpenQuestion holds

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LicenceCC BY
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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.