Affiliation:
1. National Nutrition Institute
2. Al-Azhar University
Abstract
Abstract
Background: Childhood obesity represents a serious worldwide problem with many short and long-term significant health consequences. This study aimed to assess the expression levels of microRNA-122 and microRNA-370, and their possible correlation with insulin resistance and cardiovascular diseases in obese Egyptian children.
Methods: Seventy obese children aged 5-10 years and thirty age-matched normal weight children as control were enrolled. All children were subjected to anthropometric, systolic, and diastolic blood pressure measurements as well as the expression of circulating of microRNA-122 and microRNA-370 was measured by quantitative real-time polymerase chain reaction amplification. Serum biochemical parameters (glucose, insulin, total cholesterol, triglycerides, LDL, and HDL) levels were determined. The homeostasis model assessment version 2 (HOMA2) was used to evaluate pancreatic beta cell function (HOMA2-%B), insulin resistance (HOMA2-IR), and insulin sensitivity (HOMA2-%S). Insulin sensitivity was further assessed by the single-point insulin sensitivity estimator (SPISE) index and McAuley index.
Results: Compared with control group, the weight, BMI, fasting blood glucose, triglycerides, total cholesterol, LDL, VLDL, non-HDL cholesterol, cardiac risk ratio 1, cardiac risk ratio 2, atherogenic coefficient, atherogenic index, insulin levels, HOMA2-%B, HOMA2-IR and microRNA-122 were significantly increased (P < 0.001). MicroRNA-122 showed significant positive correlations with cardiac risk ratio 1 and atherogenic coefficient, however, a significant negative correlation with HDL in obese group. On the other hand, HOMA2-%S, McAuley and SPISE insulin sensitivity indices, HDL and microRNA-370 were significantly decreased.
Conclusions: Changes in serum level of microRNA-122 and microRNA-370 in obese children may suggest a possible role in the pathogenesis of childhood obesity and their accompanied complications. Therefore, they can serve as early biomarkers and possible predictors for future metabolic dysfunction.
Publisher
Research Square Platform LLC
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