International journal of molecular sciences · 2026
Differential Expression of microRNAs in Obese Mexican Children: Links to Insulin Resistance and Dyslipidemia.
СтатьяНаблюдательное исследованиеНазвание и аннотация: Перевод в очереди
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Contreras-Ramos Alejandra, Díaz-Rosas Guadalupe, Cruz Miguel, Nava-Cabrera Ana, Vazquez-Moreno Miguel, Gómez-Acuña Omar, Guerrero-Ortiz Ana María, Domínguez-Hernández Carmen, Pérez-Herrera Aleyda, Jiménez-Aguilar Rosalinda, Goméz-Zamudio Jaime, Gaytán-Cervantes Francisco Javier, Cid-Soto Miguel Ángel, González-Torres Carolina, Ortega-Camarillo Clara
Аннотация
To analyze, in an analytical cross-sectional observational study, the relationship between the plasma microRNA (miRNA) expression profile in children living with obesity and their metabolic health status. Based on body mass index percentiles (BMIp), the children were grouped into a control group (C) or an obesity group (Ob). Glucose, insulin, and low- and high-density lipoproteins (LDLs and HDLs, respectively), triacylglycerols (TG), and total cholesterol (TC) were measured. RNA from plasma was used for miRNA sequencing analysis (NextSeq 2000 platform). Differential miRNA expression was determined using counts obtained from the reference genome. Fifty controls (BMIp: 50.4 ± 23) and fifty children with obesity (BMIp: 97.54 ± 1.46) were included. The obese group presented hyperinsulinemia and insulin resistance. Sequencing revealed nine underexpressed and six overexpressed miRNAs in the obese group. In silico analysis suggested that these miRNAs may participate in regulating insulin secretion, protein synthesis, apoptosis, and the glycolytic pathway in pancreatic β-cells. Childhood obesity was associated with altered circulating levels of microRNAs linked to glucose metabolism, insulin resistance (IR) and β-cell survival. Reduced plasma levels of miR-126-3p, let-7a-5p, and miR-16-5p showed a high predictive value for hypertriglyceridemia and insulin resistance, indicating their potential relevance as early biomarkers or therapeutic targets in pediatric metabolic dysfunction.