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Cerebrospinal Fluid MicroRNA Profiling Using Quantitative Real Time PCR
Published on: January 22, 2014
Exosomal miRNA Profile in Small-for-Gestational-Age Children: A Potential Biomarker for Catch-Up Growth
Hwal Rim Jeong1, Jae-A Han2, Heeji Kim2
1Department of Pediatrics, College of Medicine, Soonchunhyang University, Cheonan 31151, Korea.
Insights
Small-for-gestational-age (SGA) children without catch-up growth (CU) exhibit unique exosomal microRNA (miRNA) profiles. These distinct miRNA signatures may serve as novel biomarkers for identifying growth failure in SGA infants.
Area of Science:
- Biochemistry
- Genetics
- Pediatrics
Background:
- Postnatal growth failure in small-for-gestational-age (SGA) children and the mechanisms of catch-up growth (CU) remain poorly understood.
- Exosomal microRNAs (miRNAs) are emerging as critical regulators of biological processes and potential biomarkers.
Purpose of the Study:
- To investigate the exosomal miRNA signature associated with catch-up growth in SGA children.
- To identify potential exosomal miRNA biomarkers for growth failure in SGA infants.
Main Methods:
- Serum exosomal miRNA was analyzed using next-generation sequencing (NGS) in 16 SGA children (5 with CU, 6 without CU) and 10 appropriate-for-gestational-age (AGA) children.
- Exosomal miRNA expression profiles were compared across SGA-CU, SGA-nCU, and AGA groups.
Main Results:
- Exosomal miRNA profiles clustered into three distinct groups, with SGA-nCU differing significantly from SGA-CU and AGA groups.
- 22 miRNAs were differentially expressed between SGA-nCU and AGA, 19 between SGA-nCU and SGA-CU, and 6 between SGA-CU and AGA.
- Specific miRNAs (e.g., miR-874-3p, miR-6126) showed potential as SGA biomarkers, while others (e.g., miR-30c-5p, miR-23a-5p) were linked to growth failure in SGA-nCU children.
Conclusions:
- SGA children without catch-up growth possess a distinct exosomal miRNA expression profile compared to AGA and SGA children with catch-up growth.
- Exosomal miRNAs represent promising novel biomarkers for assessing catch-up growth potential and identifying growth failure in SGA children.
Abstract:
Objective: The mechanism underlying postnatal growth failure and catch-up growth in small-for-gestational-age (SGA) children is poorly understood. This study investigated the exosomal miRNA signature associated with catch-up growth in SGA children. Methods: In total, 16 SGA and 10 appropriate-for-gestational-age (AGA) children were included. Serum exosomal miRNA was analyzed using next-generation sequencing (NGS). Exosomal miRNA was profiled for five SGA children with catch-up growth (SGA-CU), six SGA children without CU growth (SGA-nCU), and five AGA children. Results: Exosomal miRNA profiles were clustered into three clear groups. The exosomal miRNA expression profiles of the SGA-nCU group differed from those of the SGA-CU and AGA groups. In all, 22 miRNAs were differentially expressed between SGA-nCU and AGA, 19 between SGA-nCU and SGA-CU, and only 6 between SGA-CU and AGA. In both SGA-nCU and SGA-CU, miR-874-3p was upregulated and miR-6126 was downregulated. Therefore, these two miRNAs could serve as biomarkers for SGA. Compared with SGA-CU and AGA, miR-30c-5p, miR-363-3p, miR-29a-3p, and miR-29c-3p were upregulated in SGA-nCU, while miR-629-5p and miR-23a-5p were downregulated. These six miRNAs could be associated with growth failure in SGA-nCU children. Conclusions: SGA children without CU have a distinct exosomal miRNA expression profile compared with AGA and SGA children with CU. Exosomal miRNAs could serve as novel biomarkers for CU.
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