Evidence map›Paper›PMID 34611295›Full record

ArticleEuropean journal of clinical nutrition2022

Placental expression of miR-21-5p, miR-210-3p and miR-141-3p: relation to human fetoplacental growth.

P Kochhar, P Dwarkanath, G Ravikumar, A Thomas, J Crasta, T Thomas, A V Kurpad, A Mukhopadhyay

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Article in European journal of clinical nutrition, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. The effect of MicroRNAs variants on idiopathic recurrent pregnancy loss.Journal of assisted reproduction and genetics · 2023
    Article
  8. Review
  9. Article
  10. 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

8 authors at 2 institutions in 1 country.

P KochharDivision of Nutrition, St. John's Research Institute, A recognized research centre of University of Mysore, Bangalore, India.
P DwarkanathDivision of Nutrition, St. John's Research Institute, A recognized research centre of University of Mysore, Bangalore, India.ORCID http://orcid.org/0000-0002-9843-1057
G RavikumarDepartment of Pathology, St John's Medical College Hospital, Bangalore, India.ORCID http://orcid.org/0000-0002-4426-6914
A ThomasDepartment of Obstetrics and Gynaecology, St John's Medical College Hospital, Bangalore, India.
J CrastaDepartment of Pathology, St John's Medical College Hospital, Bangalore, India.
T ThomasDepartment of Biostatistics, St. John's Medical College Hospital, Bangalore, India.ORCID http://orcid.org/0000-0002-1786-6076
A V KurpadDivision of Nutrition, St. John's Research Institute, A recognized research centre of University of Mysore, Bangalore, India.ORCID http://orcid.org/0000-0001-7998-2438
A MukhopadhyayDivision of Nutrition, St. John's Research Institute, A recognized research centre of University of Mysore, Bangalore, India. arpitam@sjri.res.in.ORCID http://orcid.org/0000-0001-8260-5385
St.John's Medical College Hospital · INUniversity of Mysore · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesDysregulation of microRNAs (miRNAs) and their target genes in placental tissue is associated with foetal growth restriction. We aimed to evaluate associations of placental miR-21-5p, miR-141-3p and miR-210-3p expression with maternal, placental and newborn parameters and with placental expression of their potential target genes PTEN, VEGF, FLT and ENG in a set of well-characterized small- (SGA) and appropriate- (AGA) for gestational age full-term singleton pregnancies. SUBJECTS/

methodsPlacental samples (n = 80) from 26 SGA and 54 AGA were collected from full-term singleton pregnancies. Placental transcript abundances of miR-21-5p, miR-141-3p and miR-210-3p were assessed after normalization to a reference miRNA, mir-16-5p by real-time quantitative PCR. Placental transcript abundances of PTEN, VEGF, FLT and ENG were assessed after normalizing to a panel of reference genes.

resultsPlacental miR-21-5p transcript abundance was negatively associated with placental weight (n = 80, r = -0.222, P = 0.047) and this association was specific to the AGA births (n = 54, r = -0.292, P = 0.032). Placental transcript abundances of miR-210-3p and miR-141-3p were not associated with placental weight or birth weight in all 80 births. However, placental miR-210-3p transcript abundance was positively associated with birth weight specifically in the SGA births (n = 26, r = 0.449, P = 0.021). Placental transcript abundance of miR-21-5p was negatively associated with PTEN transcript abundance (Spearman's ρ = -0.245, P = 0.028) while that of miR-141-3p was positively associated with FLT (Spearman's ρ = 0.261, P = 0.019) and ENG (Spearman's ρ = 0.259, P = 0.020) transcript abundances in all 80 births.

conclusionWe conclude that placental miR-21-5p and miR-210-3p may be involved in fetoplacental growth. However, this regulation is unlikely to be mediated through placental expression of PTEN, VEGF, FLT or ENG.

Indexed as

MicroRNAsPlacentaBirth WeightFemaleFetal Growth RetardationHumansInfant, NewbornPregnancyVascular Endothelial Growth Factor AMicroRNAsMIRN141 microRNA, humanMIRN210 microRNA, humanMIRN21 microRNA, humanVascular Endothelial Growth Factor A

Identifiers

PMID34611295
OpenAlexW3204693898

What OpenQuestion holds

Textmetadata
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.