Evidence map›Paper›PMID 34159524›Full record

ArticleIrish journal of medical science2022

MiR-590-3p and its targets VEGF, PIGF, and MMP9 in early, middle, and late pregnancy: their longitudinal changes and correlations with risk of fetal growth restriction.

Jindan Pei, Yan Li, Zhihong Min, Qi Dong, Jiali Ruan, Juan Wu, Xiaolin Hua

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In one paragraph

Article in Irish journal of medical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Differential Effects ofNutrients · 2024
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. The Role of Syncytin in Placental Angiogenesis and Fetal Growth.Frontiers in cell and developmental biology · 2022
    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

7 authors at 2 institutions in 1 country.

Jindan PeiDepartment of Gynecology, Shanghai First Maternity and Infant Hospital, 2699 West Gaoke Road, Shanghai, 201204, China.
Yan LiDepartment of Gynecology, Shanghai First Maternity and Infant Hospital, 2699 West Gaoke Road, Shanghai, 201204, China.
Zhihong MinDepartment of Gynecology, Shanghai First Maternity and Infant Hospital, 2699 West Gaoke Road, Shanghai, 201204, China.
Qi DongDepartment of Gynecology, Shanghai First Maternity and Infant Hospital, 2699 West Gaoke Road, Shanghai, 201204, China.
Jiali RuanDepartment of Gynecology, Shanghai First Maternity and Infant Hospital, 2699 West Gaoke Road, Shanghai, 201204, China.
Juan WuDepartment of Gynecology, Tenth People's Hospital of Tongji University, Shanghai, China.
Xiaolin HuaDepartment of Gynecology, Shanghai First Maternity and Infant Hospital, 2699 West Gaoke Road, Shanghai, 201204, China. huaxiaolin_sh@163.com.ORCID http://orcid.org/0000-0002-5996-6577
Shanghai First Maternity and Infant Hospital · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe term "fetal growth restriction (FGR)" is commonly used to describe fetuses with an estimated fetal weight that is less than 10th percentile for gestational age. This study aimed to investigate the longitudinal change of microRNA-590-3p (miR-590-3p), vascular endothelial growth factor (VEGF), placental growth factor (PIGF), and matrix metalloproteinase (MMP)9 expressions in early, middle, and late pregnancy, and their correlations with the fetal growth restriction (FGR) risk.

methodsTotally, 970 pregnant women in early pregnancy were enrolled, and their plasma samples were, respectively, acquired in early pregnancy (at 10th or 11th week of gestational age), middle pregnancy (at 20th or 21st week of gestational age), and late pregnancy (at 33th or 34th week of gestational age) for miR-590-3p, VEGF, PIGF, and MMP9 determinations.

resultsMiR-590-3p underwent a growing trend, but VEGF, PIGF, and MMP9 experienced declined trend along with pregnancy (all P < 0.001). Furthermore, the negative association of miR-590-3p with VEGF, PIGF, and MMP9 became stronger along with the pregnancy. Besides, miR-590-3p expression in middle and late pregnancy was higher, but VEGF, PIGF, and MMP9 expressions in middle and late pregnancy were lower in women affected by FGR compared to normal pregnant women (all P < 0.001). In addition, miR-590-3p, VEGF, PIGF, and MMP9 expression in middle and late pregnancy were of good value in predicting FGR risk.

conclusionsmiR-590-3p exhibits a growing trend during pregnancy, and its expression in middle and late pregnancy is associated with increased FGR risk via interaction with VEGF, PIGF, and MMP9.

Indexed as

Fetal Growth RetardationMicroRNAsFemaleHumansMatrix Metalloproteinase 9Placenta Growth FactorPregnancyVascular Endothelial Growth Factor AMatrix Metalloproteinase 9MicroRNAsMIRN590 microRNA, humanMMP9 protein, humanPGF protein, humanPlacenta Growth FactorVascular Endothelial Growth Factor AVEGFA protein, humanFetal growth restrictionMatrix metalloproteinase 9MicroRNA-590-3pPlacental growth factorVascular endothelial growth factor

Identifiers

PMID34159524
OpenAlexW3176060219

What OpenQuestion 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 OpenQuestion graph.