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Title: Pre-pregnancy BMI-associated miRNA and mRNA expression signatures in the placenta highlight a sexually-dimorphic response to maternal underweight status.

Authors: Clark, Jeliyah; Eaves, Lauren A; Gaona, Adriana R; Santos Jr, Hudson P; Smeester, Lisa; Bangma, Jacqueline T; Rager, Julia E; O'Shea, T Michael; Fry, Rebecca C

Published In Sci Rep, (2021 Aug 03)

Abstract: Pre-pregnancy body mass index (BMI) is associated with adverse pregnancy and neonatal health outcomes, with differences in risk observed between sexes. Given that the placenta is a sexually dimorphic organ and critical regulator of development, examining differences in placental mRNA and miRNA expression in relation to pre-pregnancy BMI may provide insight into responses to maternal BMI in utero. Here, genome-wide mRNA and miRNA expression levels were assessed in the placentas of infants born extremely preterm. Differences in expression were evaluated according to pre-pregnancy BMI status (1) overall and (2) in male and female placentas separately. Overall, 719 mRNAs were differentially expressed in relation to underweight status. Unexpectedly, no genes were differentially expressed in relation to overweight or obese status. In male placentas, 572 mRNAs were associated with underweight status, with 503 (70%) overlapping genes identified overall. Notably, 43/572 (8%) of the mRNAs associated with underweight status in male placentas were also gene targets of two miRNAs (miR-4057 and miR-128-1-5p) associated with underweight status in male placentas. Pathways regulating placental nutrient metabolism and angiogenesis were among those enriched in mRNAs associated with underweight status in males. This study is among the first to highlight a sexually dimorphic response to low pre-pregnancy BMI in the placenta.

PubMed ID: 34344912 Exiting the NIEHS site

MeSH Terms: Adolescent; Adult; Body Mass Index*; Female; Humans; Infant, Newborn; Male; MicroRNAs/genetics*; Middle Aged; Obesity/physiopathology*; Placenta/metabolism; Placenta/pathology*; Pregnancy; RNA, Messenger/genetics; RNA, Messenger/metabolism*; Sex Characteristics*; Thinness/physiopathology*; Young Adult

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