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Duration of the pushing phase of labor is inversely associated with expression of TNF, IL6, IGF1 and IGF2 in human placenta.

Authors :
Lodefalk, Maria
Allbrand, Marianne
Montgomery, Scott
Source :
Journal of Maternal-Fetal & Neonatal Medicine. Dec2022, Vol. 35 Issue 25, p6476-6482. 7p.
Publication Year :
2022

Abstract

Objective Gene expression in placenta differs between vaginal and cesarean deliveries, but the influence of the duration of labor on placental gene expression is incompletely known. Our aim was to investigate associations between duration of labor and expression of some genes involved in growth or inflammation in human placental tissue. Methods Placenta samples (n = 126) were collected after an uncomplicated, singleton pregnancy and term vaginal delivery at Örebro University Hospital, Sweden. Duration of labor was recorded by the midwife in the delivery room. The expression of the following genes was analyzed by RT-qPCR: tumor necrosis factor (TNF), interleukin-6 (IL6), C-X-C motif chemokine ligand 8, toll-like receptor (TLR) 2, TLR4, insulin receptor, insulin-like growth factor (IGF) 1, IGF2, leptin, hepatocyte growth factor (HGF) and HGF receptor (MET). Multivariable linear regression models were used for the evaluation of associations with labor duration adjusting for potential confounding factors. The Benjamini-Hoschberg method was used to correct for multiple testing. Results The expression of TNF, IL6, IGF1 and IGF2 was inversely associated with the duration of the pushing phase of labor (B coefficients (95% confidence interval) = −0.150 (−0.277 to −0.023), −0.159 (−0.289 to −0.029), −0.099 (−0.176 to −0.021), and −0.081 (−0.145 to −0.017), respectively). Conclusions Longer duration of pushing is associated with downregulation of the expression of genes in placenta from vaginal deliveries. Future research on gene expression in labored placenta should take into account associations with labor duration and especially the pushing phase. Potential impact of these associations on the mother, the fetus and the new-born infant should also be explored. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14767058
Volume :
35
Issue :
25
Database :
Academic Search Index
Journal :
Journal of Maternal-Fetal & Neonatal Medicine
Publication Type :
Academic Journal
Accession number :
161126229
Full Text :
https://doi.org/10.1080/14767058.2021.1916459