Evidence map›Paper›PMID 42246310›Full record

ArticleTurkish journal of obstetrics and gynecology2026

Long non-coding RNA maternally expressed gene 3 (

Shaghayegh Saljoughi, Hasan Dana, Mahtab Norouzi, Hossein Shahraki Ghadimi, Marzieh Ghasemi, Mansooreh Zargar, Mohsen Saravani

Abstract read
In one paragraph

Article in Turkish journal of obstetrics and gynecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Shaghayegh SaljoughiGenetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID 0000-0003-4601-4232
Hasan DanaGenetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID 0009-0002-5053-437X
Mahtab NorouziGenetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID 0000-0003-3888-4510
Hossein Shahraki GhadimiGenetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID 0000-0002-4207-2075
Marzieh GhasemiPregnancy Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID 0000-0001-9479-0119
Mansooreh ZargarPregnancy Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID 0000-0002-0526-887X
Mohsen SaravaniGenetics of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.ORCID 0000-0001-8492-673X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Preeclampsia (PE), a significant challenge for health systems, is a hypertensive disorder of pregnancy. Some studies have suggested that long non-coding ribonucleic acids play a major role in the pathogenesis of PE by regulating the biological behaviors of maternal vascular smooth muscle cells and trophoblasts. In this study, the impact of the maternally expressed gene 3 (MEG3) rs4081134 gene polymorphism on susceptibility to PE has been evaluated. Materials and Methods: We conducted a case-control study comprising 130 PE patients and 140 normotensive pregnant women with normal gestational outcomes. Genotype analysis was performed using the polymerase chain reaction-restriction fragment length polymorphism method. Results: A significant association was evident between the AA genotype and PE risk under the recessive model, indicating that these may serve as protective factors against the development of PE. No significant relationships were detected between other genotypes, genetic models, or allelic distributions and PE risk. Additionally, among pregnant women with PE, a notable correlation was observed between newborn birth weight and the rs4081134 polymorphism in the Conclusion: We found a significant association between the AA genotype, as well as the recessive model of the

Indexed as

geneMaternally expressed gene 3polymorphismpreeclampsia

Identifiers

PMID42246310
PMCPMC13238185

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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.