Factors affecting cord blood leptin levels in a consecutive birth cohort.


Journal

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
ISSN: 1476-4954
Titre abrégé: J Matern Fetal Neonatal Med
Pays: England
ID NLM: 101136916

Informations de publication

Date de publication:
Mar 2022
Historique:
pubmed: 1 7 2020
medline: 11 2 2022
entrez: 30 6 2020
Statut: ppublish

Résumé

The fetus that fails to meet its ideal growth trajectory has increased risks of poor health outcomes throughout life. "Gold standard" methods of anthropometric assessment such as measurement of percentage body fat can be difficult to apply across populations and other biomarkers such as serum concentration of umbilical cord blood leptin may be more effective for screening. This study reports cord blood leptin levels in a large prospective consecutive birth cohort and assesses the relationship between leptin and neonatal and maternal factors. Venous umbilical cord blood samples were collected from a prospective consecutive cohort of pregnancies at the time of delivery. Maternal and neonatal characteristics and details of delivery were collated. Serum leptin levels were measured, associations with demographic features were identified, and a normal range was established. The association between cord leptin level and neonatal outcome was tested. Umbilical cord leptin and maternal and neonatal characteristics were collected at 1275 births. The median leptin value was 10.8 ng/ml (IQR: 6.4, 17.8 ng/ml). Log Neonatal cord leptin levels are influenced by a number of maternal and fetal characteristics. Absolute levels can be adjusted to account for normal population variation. Infants requiring admission to NICU have lower mean leptin MoM levels. Further studies are needed to see whether the identification of fetuses with polarized leptin levels (<5th or >95th centile) will benefit from further surveillance or intervention in infancy.

Identifiants

pubmed: 32594793
doi: 10.1080/14767058.2020.1733518
doi:

Substances chimiques

LEP protein, human 0
Leptin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

884-889

Auteurs

Rina Fyfe (R)

Sydney Institute for Women, Children and their Families, Sydney Local Health District, Sydney, Australia.
Department of Obstetrics and Gynaecology, University of Newcastle, Newcastle, Australia.

Alice Burton (A)

Sydney Institute for Women, Children and their Families, Sydney Local Health District, Sydney, Australia.

Andrew McLennan (A)

Sydney Institute for Women, Children and their Families, Sydney Local Health District, Sydney, Australia.
Discipline of Obstetrics, Gynaecology and Neonatology, Faculty of Medicine, University of Sydney, Sydney, Australia.

Lucy McCudden (L)

Sydney Institute for Women, Children and their Families, Sydney Local Health District, Sydney, Australia.

Adrienne Gordon (A)

Sydney Institute for Women, Children and their Families, Sydney Local Health District, Sydney, Australia.
Discipline of Obstetrics, Gynaecology and Neonatology, Faculty of Medicine, University of Sydney, Sydney, Australia.

Jon Hyett (J)

Sydney Institute for Women, Children and their Families, Sydney Local Health District, Sydney, Australia.
Discipline of Obstetrics, Gynaecology and Neonatology, Faculty of Medicine, University of Sydney, Sydney, Australia.

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Classifications MeSH