DLK1: A Novel Biomarker of Placental Insufficiency in Stillbirth and Live Birth.


Journal

American journal of perinatology
ISSN: 1098-8785
Titre abrégé: Am J Perinatol
Pays: United States
ID NLM: 8405212

Informations de publication

Date de publication:
22 Aug 2022
Historique:
pubmed: 17 6 2022
medline: 17 6 2022
entrez: 16 6 2022
Statut: aheadofprint

Résumé

 Delta-like homolog 1 (DLK1) is a growth factor that is reduced in maternal sera in pregnancies with small for gestational age neonates. We sought to determine if DLK1 is associated with stillbirth (SB), with and without placental insufficiency.  A nested case-control study was performed using maternal sera from a multicenter case-control study of SB and live birth (LB). SB and LB were stratified as placental insufficiency cases (small for gestational age <5% or circulatory lesions on placental histopathology) or normal placenta controls (appropriate for gestational age and no circulatory lesions). Enzyme-linked immunosorbent assay (ELISA) was used to measure DLK1. The mean difference in DLK1 was compared on the log scale in an adjusted linear regression model with pairwise differences, stratified by term/preterm deliveries among DLK1 results in the quantifiable range. In exploratory analysis, geometric means were compared among all data and the proportion of "low DLK1" (less than the median value for gestational age) was compared between groups and modeled using linear and logistic regression, respectively.  Overall, 234 SB and 234 LB were analyzed; 246 DLK1 values were quantifiable within the standard curve. Pairwise comparisons of case and control DLK1 geometric means showed no significant differences between groups. In exploratory analysis of all data, adjusted analysis revealed a significant difference for the LB comparison only (SB: 71.9 vs. 99.1 pg/mL,  In exploratory analysis, more placental insufficiency cases in preterm SB and LB had "low DLK1." However, low DLK1 levels were not associated with SB. · Maternally circulating DLK1 is correlated with placental insufficiency.. · Maternally circulating DLK1 is not correlated with SB.. · DLK1 is a promising marker for placental insufficiency..

Identifiants

pubmed: 35709732
doi: 10.1055/a-1877-6191
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : 8UL1TR000105,U01-HD045954 ,U01-HD087182 ,U10-HD045925 ,U10-HD045944,U10-HD045952 ,U10-HD045953 ,U10-HDO45955
ID : NIH Clinical Center

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

None declared.

Auteurs

Jessica M Page (JM)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah Health Sciences, Salt Lake City, Utah.
Division of Maternal-Fetal Medicine, Intermountain Health Care, Murray, Utah.

Amanda A Allshouse (AA)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah Health Sciences, Salt Lake City, Utah.

Jessica E Gaffney (JE)

Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center Oregon Health and Science University, Portland, Oregon.

Victoria H J Roberts (VHJ)

Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center Oregon Health and Science University, Portland, Oregon.

Vanessa Thorsten (V)

RTI International, Research Triangle Park, North Carolina.

Karen J Gibbins (KJ)

Department of Obstetrics and Gynecology, Oregon Health and Science University, Portland, Oregon.

Donald J Dudley (DJ)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Virginia, Charlottesville, Virginia.

George Saade (G)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Texas Medical Branch at Galveston.

Robert L Goldenberg (RL)

Department of Obstetrics and Gynecology, Columbia University, New York, New York.

Barbara J Stoll (BJ)

Department of Pediatrics, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, Texas.

Carol J Hogue (CJ)

Rollins School of Public Health, Emory University, Atlanta, Georgia.

Radek Bukowski (R)

Department of Women's Health, Dell Medical School, University of Texas at Austin, Austin, Texas.

Corette Parker (C)

RTI International, Research Triangle Park, North Carolina.

Deborah Conway (D)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.

Uma M Reddy (UM)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Yale School of Medicine, New Haven, Connecticut.

Michael W Varner (MW)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah Health Sciences, Salt Lake City, Utah.
Division of Maternal-Fetal Medicine, Intermountain Health Care, Murray, Utah.

Antonio E Frias (AE)

Department of Obstetrics and Gynecology, Oregon Health and Science University, Portland, Oregon.

Robert M Silver (RM)

Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah Health Sciences, Salt Lake City, Utah.
Division of Maternal-Fetal Medicine, Intermountain Health Care, Murray, Utah.

Classifications MeSH