Umbilical Cord miRNAs in Small-for-Gestational-Age Children and Association With Catch-Up Growth: A Pilot Study

Berta Mas-Parés1, Sílvia Xargay-Torrent2, Alexandra Bonmatí3

  • 1Maternal-Fetal Metabolic Research Group, Girona Institute for Biomedical Research, Salt, Spain.

Insights

Catch-up growth in infants small for gestational age (SGA) is linked to adult cardiometabolic diseases. Umbilical cord microRNAs (miRNAs), particularly miR-576-5p, may predict this growth and associated health risks.

Area of Science:

  • Perinatal biology
  • Developmental origins of health and disease
  • Molecular biology

Background:

  • Catch-up growth in infants small for gestational age (SGA) is a known risk factor for adult cardiometabolic diseases.
  • The underlying mechanisms of catch-up growth in SGA newborns are not well understood.

Purpose of the Study:

  • To identify specific umbilical cord microRNAs (miRNAs) associated with catch-up growth in SGA infants.
  • To investigate the relationship between these miRNAs and the offspring's cardiometabolic parameters over time.

Main Methods:

  • Utilized miRNA PCR panels to analyze miRNA profiles in umbilical cord tissue from SGA infants with and without catch-up growth, and appropriate for gestational age (AGA) controls.
  • Validated significant miRNAs in a larger cohort and correlated them with anthropometric measurements at 1 and 6 years of age.

Main Results:

  • Several miRNAs, including miR-501-3p, miR-576-5p, miR-770-5p, and miR-876-3p, showed associations with growth parameters at 1 year.
  • miR-576-5p emerged as a significant predictor of catch-up growth at 1 year and cardiometabolic risk factors (weight, waist, renal fat) at 6 years.
  • In silico analysis indicated miR-576-5p's role in regulating inflammatory and growth pathways.

Conclusions:

  • Umbilical cord miRNAs show potential as early biomarkers for identifying catch-up growth in SGA infants.
  • miR-576-5p may play a crucial role in regulating postnatal growth and influencing the risk of cardiometabolic diseases linked to prenatal-postnatal growth discrepancies.
Abstract

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