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Published on: September 14, 2017
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.
Context:
Catch-up growth in infants who are small for gestational age (SGA) is a risk factor for the development of cardiometabolic diseases in adulthood. The basis and mechanisms underpinning catch-up growth in newborns who are SGA are unknown.
Objective:
To identify umbilical cord miRNAs associated with catch-up growth in infants who are SGA and study their relationship with offspring's cardiometabolic parameters.
Design:
miRNA PCR panels were used to study the miRNA profile in umbilical cord tissue of five infants who were SGA with catch-up (SGA-CU), five without catch-up (SGA-nonCU), and five control infants [appropriate for gestational age (AGA)]. The miRNAs with the smallest nominal P values were validated in 64 infants (22 AGA, 18 SGA-nonCU, and 24 SGA-CU) and correlated with anthropometric parameters at 1 (n = 64) and 6 years of age (n = 30).
Results:
miR-501-3p, miR-576-5p, miR-770-5p, and miR-876-3p had nominally significant associations with increased weight, height, weight catch-up, and height catch-up at 1 year, and miR-374b-3p, miR-548c-5p, and miR-576-5p had nominally significant associations with increased weight, height, waist, hip, and renal fat at 6 years. Multivariate analysis suggested miR-576-5p as a predictor of weight catch-up and height catch-up at 1 year, as well as weight, waist, and renal fat at 6 years. In silico studies suggested that miR-576-5p participates in the regulation of inflammatory, growth, and proliferation signaling pathways.
Conclusions:
Umbilical cord miRNAs could be novel biomarkers for the early identification of catch-up growth in infants who are SGA. miR-576-5p may contribute to the regulation of postnatal growth and influence the risk for cardiometabolic diseases associated with a mismatch between prenatal and postnatal weight gain.
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