Placental expression of miR-517-5p and miR-518f-5p: Fetal sex-specific relations with human fetoplacental growth.


Journal

European journal of obstetrics, gynecology, and reproductive biology
ISSN: 1872-7654
Titre abrégé: Eur J Obstet Gynecol Reprod Biol
Pays: Ireland
ID NLM: 0375672

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 23 10 2021
accepted: 23 12 2021
pubmed: 8 1 2022
medline: 3 2 2022
entrez: 7 1 2022
Statut: ppublish

Résumé

We aimed to assess association of chromosome 19 miRNA cluster microRNAs (miR-517-5p and miR-518f-5p) expression with maternal, placental and newborn parameters and with their potential angiogenesis-associated target genes ENG, VEGF and FLT in a set of 68 small- (SGA, n = 30) and appropriate- (AGA, n = 38) for gestational age full-term singleton pregnancies, in relation to fetal sex. In this retrospective case-control study, placental transcript abundances of miR-517-5p and miR-518f-5p were assessed by real-time quantitative PCR after normalization to reference miRNA, mir-16-5p. Placental transcript abundances of VEGF, FLT and ENG were assessed after normalizing to a set of reference genes. Placental miR-517-5p transcript abundance was negatively associated with birth weight [β = -88.778, P = 0.006, 95% confidence interval (CI): -151.645, -25.911] and placental weight (β = -14.683, P = 0.007, 95% CI: -25.254, -4.112) and this association with birth weight was specific to the AGA births (β = -59.207, P = 0.037, 95% CI: -114.522, -3.891). miR-518f-5p transcript abundance was negatively associated with placental weight (β = -6.250, P = 0.034, 95% CI: -11.940, -0.559) specifically in the AGA male births (n = 16). Placental VEGF transcript abundance was negatively associated with that of miR-517-5p specifically in SGA female births (n = 14; Spearman's ρ = -0.705, P = 0.005) and with miR-518f-5p transcript abundance specifically in SGA births (Spearman's ρ = -0.437, P = 0.016) and in SGA male births (n = 16; Spearman's ρ = -0.516, P = 0.041). We conclude that placental miR-517-5p could be playing a key role in the pathophysiology of fetal growth restriction, which can be potentially targeted through maternal lifestyle modifications for improving fetoplacental growth.

Identifiants

pubmed: 34992034
pii: S0301-2115(21)01037-X
doi: 10.1016/j.ejogrb.2021.12.030
pii:
doi:

Substances chimiques

MIRN517 microRNA, human 0
MicroRNAs 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

118-125

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Prachi Kochhar (P)

Division of Nutrition, St. John's Research Institute, A Recognized Research Centre of University of Mysore, Bangalore, India.

Pratibha Dwarkanath (P)

Division of Nutrition, St. John's Research Institute, A Recognized Research Centre of University of Mysore, Bangalore, India.

Gayatri Ravikumar (G)

Department of Pathology, St John's Medical College Hospital, Bangalore, India.

Annamma Thomas (A)

Department of Obstetrics and Gynaecology, St John's Medical College Hospital, Bangalore, India.

Julian Crasta (J)

Department of Pathology, St John's Medical College Hospital, Bangalore, India.

Tinku Thomas (T)

Department of Biostatistics, St. John's Medical College Hospital, Bangalore, India.

Anura V Kurpad (AV)

Division of Nutrition, St. John's Research Institute, A Recognized Research Centre of University of Mysore, Bangalore, India.

Arpita Mukhopadhyay (A)

Division of Nutrition, St. John's Research Institute, A Recognized Research Centre of University of Mysore, Bangalore, India. Electronic address: arpitam@sjri.res.in.

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Classifications MeSH