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Published on: July 27, 2016
Identification of novel circulating miRNAs biomarkers for healthy obese and lean children
Feifei Ma1,2, Dingding Cao1, Zhuo Liu1
1Department of Biochemistry and Immunology, Capital Institute of Pediatrics, 2 Yabao street, Beijing, 100020, People's Republic of China.
Insights
Childhood obesity is rising globally. This study identified specific circulating microRNAs (miRNAs), hsa-miR-15b-5p and hsa-miR-223-3p, as potential biomarkers for early detection of pediatric obesity and associated metabolic risks.
Area of Science:
- Molecular Biology
- Genetics
- Biomarker Discovery
Background:
- Global rise in childhood obesity and overweight cases.
- Associated increase in metabolic disorders among children.
- Complex etiology involving genetic, epigenetic, and environmental factors.
Purpose of the Study:
- Identify circulating microRNAs (miRNAs) as potential biomarkers for pediatric obesity.
- Investigate the correlation between specific miRNAs and obesity in children.
- Explore the role of miRNAs in underlying metabolic abnormalities.
Main Methods:
- Plasma miRNA expression profiling using miRNA microarrays in obese and lean children.
- Validation of differentially expressed miRNAs via TaqMan quantitative real-time PCR (qPCR).
- Statistical analysis including multiple linear regression, ROC curve analysis, and odds ratio calculations.
- Bioinformatic identification of miRNA target genes and pathway analysis.
Main Results:
- Thirty-six differentially expressed miRNAs identified; seven validated by qPCR.
- Upregulation of hsa-miR-15b-5p and hsa-miR-223-3p confirmed, showing significant association with obesity.
- These miRNAs demonstrated strong diagnostic potential (AUC up to 0.929) and correlated with obesity risk.
- hsa-miR-15b-5p targets genes in key metabolic pathways like insulin and AMPK signaling.
Conclusions:
- Circulating miRNA expression profiles reflect metabolic abnormalities in obese children.
- Hsa-miR-15b-5p and hsa-miR-223-3p show promise as molecular markers for screening obese children.
- These miRNAs could aid in identifying populations at risk for metabolic syndrome.
Background:
The prevalence of childhood obesity and overweight has risen globally, leading to increased rates of metabolic disorders. Various factors, including genetic, epigenetic, and environmental influences such as diet and physical activity, contribute to pediatric obesity. This study aimed to identify specific circulating miRNAs as potential biomarkers for assessing obesity in children.
Methods:
Thirty children, including 15 obese and 15 extremely thin individuals, were selected for this study. MiRNA expression in circulating plasma was assessed using miRNA microarrays. The reliability of differential miRNA expression was confirmed using TaqMan qPCR. The correlation between miRNAs and obesity was analyzed through multiple linear regression, receiver operator characteristic (ROC) curve analysis, and odds ratio (OR) calculations. Bioinformatics tools were utilized to identify target genes for the selected miRNAs, and a functional network map was constructed.
Results:
A total of 36 differentially expressed miRNAs were identified through gene chip analysis, and TaqMan qPCR validation confirmed the upregulation of seven miRNAs: hsa-miR-126-3p, hsa-miR-15b-5p, hsa-miR-199a-3p, hsa-miR-20a-5p, hsa-miR-223-3p, hsa-miR-23a-3p, and hsa-miR-24-3p. Among these, hsa-miR-15b-5p and hsa-miR-223-3p exhibited a statistically significant difference except for hsa-miR-23a-3p. These two miRNAs showed more predicted target genes related to obesity than others. Multiple linear regression analysis revealed an association between obesity and hsa-miR-15b-5p and hsa-miR-223-3p [10.529 (4.974-16.084), -10.225 (-17.852~ -2.657)]. Even after adjusting for age and sex, these two miRNAs remained associated with obesity [8.936 (3.572-14.301), -8.449(-15.634~ -1.303)]. The area under the ROC curve (AUC) reached values of 0.816, 0.711, and 0.929, respectively. Odds ratio analysis demonstrated a significant correlation between obesity and hsa-miR-15b-5p (OR = 143, 95% CI 5.80 to 56,313, p = 0.024) and between obesity and hsa-miR-223-3p (OR = 0.01, 95% CI 0.00 to 0.23, p = 0.037). Importantly, hsa-miR-15b-5p was found to have numerous target genes associated with the FoxO, insulin, Ras, and AMPK signaling pathways.
Conclusions:
Differential miRNA expression profiles in the circulation of obese children compared to controls suggest underlying metabolic abnormalities. Hsa-miR-15b-5p and hsa-miR-223-3p may be considered as molecular markers for the screening of obese children and populations at risk of developing metabolic syndrome.
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