4.5 Article

Gene expression of leptin, leptin receptor isoforms and inflammatory cytokines in placentas of obese women-Associations to birth weight and fetal sex

Journal

PLACENTA
Volume 117, Issue -, Pages 64-71

Publisher

W B SAUNDERS CO LTD
DOI: 10.1016/j.placenta.2021.10.002

Keywords

Placenta; Obesity; Leptin; Cytokine; Gene expression; Infant birth weight

Funding

  1. Research Committee of Region Orebro County
  2. Nyckelfonden, Orebro University Hospital

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This study investigated the relationship between placental gene expression of leptin, its receptor, and inflammatory cytokines in obese mothers and offspring birth weight and sex. The findings revealed a reverse U-shaped association between placental leptin expression and birth weight z-scores, with higher z-scores in female infants. Additionally, the expression of different genes differed by sex, suggesting a complex regulation of fetal growth by placental leptin signaling in maternal obesity.
Introduction: Leptin signaling in placentas of obese women may influence fetal growth and may be dependent on fetal sex. The aim of this study was to investigate placental gene expression of leptin, its receptor and inflammatory cytokines in obese mothers in relation to offspring birth weight and sex. Methods: In total, 109 placental tissue samples from severely obese women (body mass index in first trimester >= 35 kg/m2) giving birth vaginally at term to a healthy child were included. Quantitative real-time PCR was used for the analysis of leptin (LEP), its receptor LEPR with two splice variants, interleukin (IL)1B, chemokine (C-X-C motif) ligand 8 (CXCL8), tumour necrosis factor (TNF), IL6, IL10, hypoxia-inducible factor 1-alpha (HIF1A) and insulin receptor (INSR). The subjects were divided into three groups based on LEP expression percentiles (<25th percentile; 25-75th percentile and >75th percentile). Results: A reverse U-shaped association between LEP expression and birth weight z-scores was found (R2 = 0.075, p = 0.005). Placental LEPRb expression was downregulated (p = 0.034) in those with highest LEP expression. Female infants had higher birth weight z-scores than males (0.58 (- 1.49-2.88) vs 0.21 (- 1.50-2.93), p = 0.020) and their placental LEPRb expression was upregulated (p = 0.047). The associations between expression of different genes differed by sex. Discussion: A reverse U-shaped relationship between placental LEP expression and offspring birth weight z-scores was found together with sexual dimorphism in LEPRb expression indicating a complex regulation of fetal growth by placental leptin signaling in maternal obesity.

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