Evidence map›Paper›PMID 34799665›Full record

ArticlePediatric research2022

microRNAs in newborns with low birth weight: relation to birth size and body composition.

Cristina Garcia-Beltran, Gemma Carreras-Badosa, Judit Bassols, Rita Malpique, Cristina Plou, Francis de Zegher, Abel López-Bermejo, Lourdes Ibáñez

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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

Cristina Garcia-BeltranEndocrinology Department, Pediatric Research Institute Hospital Sant Joan de Déu, University of Barcelona, 08950, Esplugues, Barcelona, Spain.
Gemma Carreras-BadosaPediatric Endocrinology Research Group, Girona Institute for Biomedical Research, 17190, Salt, Spain.
Judit BassolsMaternal-Fetal Metabolic Research Group, Girona Institute for Biomedical Research, 17190, Salt, Spain.
Rita MalpiqueEndocrinology Department, Pediatric Research Institute Hospital Sant Joan de Déu, University of Barcelona, 08950, Esplugues, Barcelona, Spain.
Cristina PlouEndocrinology Department, Pediatric Research Institute Hospital Sant Joan de Déu, University of Barcelona, 08950, Esplugues, Barcelona, Spain.
Francis de ZegherDepartment of Development & Regeneration, University of Leuven, 3000, Leuven, Belgium.
Abel López-BermejoPediatric Endocrinology Research Group, Girona Institute for Biomedical Research, 17190, Salt, Spain.
Lourdes IbáñezEndocrinology Department, Pediatric Research Institute Hospital Sant Joan de Déu, University of Barcelona, 08950, Esplugues, Barcelona, Spain. lourdes.ibanez@sjd.es.
Institut d'Investigació Biomèdica de Girona · ESCentro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas · ESInstituto de Salud Carlos III · ESKU Leuven · BEUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildren with low birth weight (LBW) have a higher risk of developing endocrine-metabolic disorders later in life. Deregulation of specific microRNAs (miRNAs) could underscore the programming of adult pathologies. We analyzed the miRNA expression pattern in both umbilical cord serum samples from LBW and appropriate-for-gestational-age (AGA) newborns and maternal serum samples in the 3rd trimester of gestation, and delineated the relationships with fetal growth, body composition, and markers of metabolic risk.

methodsSerum samples of 12 selected mother-newborn pairs, including 6 LBW and 6 AGA newborns, were used for assessing miRNA profile by RNA-sequencing. The miRNAs with differential expression were validated in a larger cohort [49 maternal samples and 49 umbilical cord samples (24 LBW, 25 AGA)] by RT-qPCR. Anthropometric, endocrine-metabolic markers and body composition (by DXA) in infants were determined longitudinally over 12 months.

resultsLBW newborns presented reduced circulating concentrations of miR-191-3p (P = 0.015). miR-191-3p levels reliably differentiated LBW from AGA individuals (ROC AUC = 0.76) and were positively associated with anthropometric and body composition measures at birth and weight Z-score at 12 months (P < 0.05).

conclusionsmiR-191-3p was reliably different in LBW individuals, and could be a new player in the epigenetic mechanisms linking LBW and future endocrine-metabolic adverse outcomes. IMPACT: Children with low birth weight (LBW) have a higher risk of developing endocrine-metabolic disorders. Deregulation of specific microRNAs (miRNAs) could underscore the programming of those pathologies. miR-191-3p is downregulated in serum of LBW newborns, and its concentrations associate positively with neonatal anthropometric measures, with lean mass and bone accretion at age 15 days and with weight Z-score at age 12 months. miR-191-3p was reliably different in individuals with LBW, and could be a new player in the epigenetic mechanisms connecting LBW and future endocrine-metabolic adverse outcomes.

Indexed as

MicroRNAsAdolescentAdultBiomarkersBirth WeightBody CompositionChildFemaleFetal DevelopmentGestational AgeHumansInfantInfant, Low Birth WeightInfant, NewbornBiomarkersMicroRNAs

Identifiers

PMID34799665
OpenAlexW3213186424

What OpenQuestion holds

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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.