Small for gestational age children at risk: Identifying placenta-brain axis genes as biomarkers for early prediction

Jingjing Cheng1, Heyue Jin2, Yimin Zhang2

  • 1Anhui Provincial Key Laboratory of Environment and Population Health across the Life Course, Department of Maternal & Child and Adolescent Health, School of Public Health, Anhui Medical University, Hefei, Anhui, China; Medical School, Nanjing University, Nanjing, Jiangsu, China.

Life Sciences
|February 8, 2025
PubMed

Insights

Small for gestational age (SGA) children face higher risks of neurodevelopmental delay. Decreased RPS27A gene expression in the placenta is linked to developmental delays in SGA infants, offering potential for early detection.

Area of Science:

  • Developmental Pediatrics
  • Genetics
  • Reproductive Medicine

Background:

  • Small for gestational age (SGA) is a significant global health concern.
  • The link between SGA and neurodevelopmental delay requires further investigation.
  • Identifying placental biomarkers is crucial for early neurodevelopmental delay prediction in SGA infants.

Purpose of the Study:

  • To investigate the neurodevelopmental outcomes of SGA children.
  • To explore the placenta-brain axis in relation to neurodevelopmental delay.
  • To identify potential biomarkers for early detection of neurodevelopmental delay in SGA children.

Main Methods:

  • Assessed neurodevelopment using the Ages and Stages Questionnaire of China (ASQ-C) at 6, 18, and 48 months.
  • Analyzed placental transcriptome data from SGA and appropriate for gestational age (AGA) cohorts.
  • Validated gene expression using Real-time quantitative PCR (RT-qPCR) and developed a predictive model.

Main Results:

  • SGA children exhibited increased risk of neurodevelopmental delay at 6 and 18 months.
  • Reduced RPS27A gene expression correlated with delays in problem-solving and personal-social domains at 6 months in SGA infants.
  • Established a predictive model integrating clinical and experimental data.

Conclusions:

  • The study provides insights into the placenta-brain axis mechanisms underlying neurodevelopmental delay in SGA.
  • Experimental validation confirmed RPS27A as a potential biomarker for early detection.
  • Offers novel perspectives for timely intervention in SGA children at risk for developmental delays.
Abstract

Related Concept Videos

CRISPR01:59

CRISPR

Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced Short...
Neurulation01:30

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the anterior...
Meiosis vs. Mitosis02:57

Meiosis vs. Mitosis

Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
Human Genetics01:28

Human Genetics

Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
Gut-Brain Axis01:22

Gut-Brain Axis

The gut–brain axis is a bidirectional communication system that connects the gastrointestinal tract and the brain. This interaction is mediated through multiple pathways, including the vagus nerve, hormonal signals, immune responses, and chemical messengers produced by gut microbes.Microbial Contributions to Brain FunctionGut microbiota contributes significantly to brain function by producing neuroactive compounds. These include neuroactive compounds that influence neurotransmitters such as...