Evidence map›Paper›PMID 40658322›Full record

ArticleJournal of assisted reproduction and genetics2025

Placental miRNA profiling in assisted reproductive technology (ART) pregnancies.

Deepali Sundrani, Sucheta Patil, Aishwarya Kapare, Himanshi Yadav, Karuna Randhir, Sunitha M Kasibhatla, Sanjay Gupte, Sadhana Joshi

Abstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2025. 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
–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

1 citing paper in PubMed.

  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

8 authors.

Deepali SundraniMother and Child Health, ICMR- Collaborating Centre of Excellence (ICMR-CCoE), Bharati Vidyapeeth (Deemed to be University), Interactive Research School for Health Affairs (IRSHA), Pune, 411043, India. deepali.sundrani@bharatividyapeeth.edu.ORCID http://orcid.org/0000-0002-2403-5115
Sucheta PatilC-DAC: Centre for Development of Advanced Computing, Pune, India.
Aishwarya KapareMother and Child Health, ICMR- Collaborating Centre of Excellence (ICMR-CCoE), Bharati Vidyapeeth (Deemed to be University), Interactive Research School for Health Affairs (IRSHA), Pune, 411043, India.
Himanshi YadavMother and Child Health, ICMR- Collaborating Centre of Excellence (ICMR-CCoE), Bharati Vidyapeeth (Deemed to be University), Interactive Research School for Health Affairs (IRSHA), Pune, 411043, India.
Karuna RandhirMother and Child Health, ICMR- Collaborating Centre of Excellence (ICMR-CCoE), Bharati Vidyapeeth (Deemed to be University), Interactive Research School for Health Affairs (IRSHA), Pune, 411043, India.
Sunitha M KasibhatlaC-DAC: Centre for Development of Advanced Computing, Pune, India.
Sanjay GupteGupte Hospital and Research Centre, Pune, India.
Sadhana JoshiMother and Child Health, ICMR- Collaborating Centre of Excellence (ICMR-CCoE), Bharati Vidyapeeth (Deemed to be University), Interactive Research School for Health Affairs (IRSHA), Pune, 411043, India.

Funding

Department of Biotechnology, Ministry of Science and Technology, India BT/PR30830/MED/97/441/2018
6 · The paper itself

Abstract

purposeAssisted reproductive technology (ART) procedures are associated with placental dysfunction involving dysregulation of several molecular factors and pathways. MicroRNAs (miRNAs) are crucial epigenetic regulators involved in placental development and function. The objective was to identify differential miRNAs in the placentae of women conceived by ART procedures and explore their role by pathway analysis.

methodsFifty pregnant women who underwent ART procedure and 50 pregnant women with natural pregnancy (Non-ART group) were included in the study. Qiagen miRCURY LNA PCR Array was used to identify differential miRNAs from placental samples using qRT-PCR. Pathway enrichment analysis was performed for differentially expressed miRNAs using Enrichr integrated within ShinyGO v0.80.

resultsPlacental expression of 11 hsa-miRNAs (from 28 tested hsa-miRNAs) differed (5 upregulated and 6 downregulated) in the ART group. Pathway enrichment analysis revealed that upregulated miRNAs are associated with pathways such as vasculature development, and downregulated miRNAs were associated with xenobiotic stimulus, stress-activated MAPK cascade, circadian rhythm, insulin stimulus and secretion, cellular response to oxygen levels and fibroblast proliferation. Validation of miRNAs on larger sample size demonstrated that hsa-miR-30c-5p and hsa-miR-140a-5p were downregulated in the ART group. miRNA-mRNA target network analysis revealed that these miRNAs target 58 genes associated with regulation of VEGFA receptor signaling pathway, glomerulus vasculature development, long chain fatty-acyl-CoA biosynthesis, and apoptosis.

conclusionART procedures are associated with altered placental miRNA expression, possibly contributing to disturbed placental angiogenesis. This study identified two essential miRNAs (hsa-miR-30c-5p and hsa-miR-140a-5p) associated with ART procedures that regulate placental and fetal growth and development.

Indexed as

MicroRNAsPlacentaReproductive Techniques, AssistedAdultFemaleGene Expression ProfilingHumansPlacentationPregnancyMicroRNAsAngiogenesisAssisted reproductive technologyMiRNAPathway analysisPlacenta

Identifiers

PMID40658322
PMCPMC12559531

What Socratic holds

Textmetadata
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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 Socratic graph.