Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2022
Historique:
received: 15 12 2021
accepted: 26 01 2022
entrez: 17 3 2022
pubmed: 18 3 2022
medline: 26 4 2022
Statut: epublish

Résumé

Detecting SGA (small for gestational age) during pregnancy improves the fetal and neonatal prognosis. To date, there is no valid antenatal biomarker of SGA used in clinical practice. Maternal circulating DLK1 (delta-like non-canonical notch ligand 1) levels have been shown to be significantly lower in pregnant women at 36 weeks of gestation (WG) who delivered a SGA newborn than in controls. Data in the literature are contradictory on the association between maternal circulating DLK1 levels and placental vascular dysfunction. The objective was to determine if maternal DLK1 levels in the second trimester of pregnancy are predictive of SGA, and to assess whether the measurement of DLK1 levels in maternal blood could be a means to distinguish SGA with placental vascular dysfunction from that due to other causes. We conducted a nested cased-control study within the EDEN mother-child cohort. 193 SGA (birth weight < 10

Identifiants

pubmed: 35295988
doi: 10.3389/fendo.2022.836731
pmc: PMC8919710
doi:

Substances chimiques

Calcium-Binding Proteins 0
DLK1 protein, human 0
Membrane Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

836731

Informations de copyright

Copyright © 2022 Pham, Mitanchez, Forhan, Perin, Le Bouc, Brioude, Sobrier, Heude and Netchine.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Aurelie Pham (A)

Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, APHP, Hôpital Armand Trousseau, Service de Néonatologie, Paris, France.

Delphine Mitanchez (D)

Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, Paris, France.
Centre Hospitalier Régional Universitaire (CHRU) de Tours, Hôpital Bretonneau, Service de Néonatologie, Tours, France.

Anne Forhan (A)

Université de Paris Cité, INSERM, INRAE, Centre of Research in Epidemiology and StatisticS (CRESS), Paris, France.

Laurence Perin (L)

Sorbonne Université, APHP, Hôpital Armand Trousseau, Explorations Fonctionnelles Endocriniennes, Endocrinologie Moléculaire et Pathologies d'Empreinte, Paris, France.

Yves Le Bouc (Y)

Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, Paris, France.

Frederic Brioude (F)

Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, APHP, Hôpital Armand Trousseau, Explorations Fonctionnelles Endocriniennes, Endocrinologie Moléculaire et Pathologies d'Empreinte, Paris, France.

Marie-Laure Sobrier (ML)

Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, Paris, France.

Barbara Heude (B)

Université de Paris Cité, INSERM, INRAE, Centre of Research in Epidemiology and StatisticS (CRESS), Paris, France.

Irene Netchine (I)

Sorbonne Université, INSERM, Centre de Recherche Saint Antoine, APHP, Hôpital Armand Trousseau, Explorations Fonctionnelles Endocriniennes, Endocrinologie Moléculaire et Pathologies d'Empreinte, Paris, France.

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Classifications MeSH