Key result
Childhood obesity linked to ~33% higher AGEs/sRAGE ratio vs lean controls.
Why the study?
To define factors influencing AGEs, sRAGE, AGEs/sRAGE-ratio, and AOPPs levels and investigate changes in oxidative balance among overweight and obese children.
Is childhood overweight and obesity associated with altered AGE/RAGE-related oxidative homeostasis compared to lean controls?
Case-Control (n=77)
No
Is childhood overweight and obesity associated with altered AGE/RAGE-related oxidative homeostasis compared to lean controls?
Overweight and obese children exhibit an AGE/RAGE-related oxidative homeostasis dysregulation, suggesting early susceptibility to oxidative and inflammatory tissue damage that may contribute to long-term cardiometabolic alterations.
Answers are grounded in this paper and cite their sources.
Obesity-linked AGE/sRAGE imbalance in children may signal early oxidative risk; hypothesis-generating for cardiometabolic sequelae, prospective studies needed.
Background Advanced glycation end-products (AGEs) and their cell receptor (RAGE) are involved in the pathophysiology of cardio-metabolic diseases. Interaction of AGEs with RAGE results in increased generation of oxygen radicals and pro-inflammatory cytokines. Circulating soluble RAGE (sRAGE) interacts with AGEs in order to counterbalance the negative effects of AGEs-RAGE interaction. Objectives To define factors influencing AGEs, sRAGE, AGEs/sRAGE-ratio and advanced oxidation-protein products (AOPPs) levels and to investigate changes in oxidative balance among overweight/obese children. Materials and methods Cross-sectional, one Center, case-control study included 41 overweight and obese children aged between 5–16 years and 36 lean matched controls. Inclusion criteria were: BMI ≥ 1 SD; term birth; no genetic or endocrine causes of obesity; no associated chronic diseases neither chronic therapies. All patients underwent clinical and biochemical investigations (lipid and glucose profiles, liver, renal and thyroid function tests, uric acid, C-reactive protein (CRP), AGEs, sRAGE and AOPPs serum concentrations). Significance was established at 0.050. Results AOPPs, AGEs/sRAGE-ratio, HOMA-IR, triglycerides, triglycerides/HDL-ratio, total cholesterol (TC)/HDL-ratio, atherogenic-index of plasma (AIP), uric acid, CRP were significantly higher, whereas sRAGE and HDL were significantly lower in overweight/obese children than controls. sRAGE was significantly negatively correlated with BMI SD, TC/HDL-ratio, CRP, AOPPs and positively with HDL. AGE/sRAGE-ratio and AOPPs were significantly positively correlated with BMI SD, TC/HDL-ratio, AIP, CRP, and negatively with HDL. BMI SD was independently associated with AGEs/sRAGE-ratio (B=0.06; p= 0.008), AOPPs (B=0.13; p=0.02) and sRAGE (B= -73.18; p=0.000). Conclusions We demonstrated, for the first time in a pediatric cohort, a significant higher value of AGEs/sRAGE-ratio among overweight/obese children, expression of a relative shift to oxidant from anti-oxidant factors, suggesting an AGE/RAGE-related oxidative homeostasis dysregulation that could enhance susceptibility to oxidative/inflammatory tissues damage. Severity of overweight, influencing the increase of oxidative stress in human organism and even in children, may contribute to the pathogenesis of long-term cardiovascular and metabolic alterations.
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Corica et al. (2019) conducted a case-control in Childhood obesity (n=77). Overweight and obesity vs. Lean matched controls was evaluated on AGEs/sRAGE-ratio (p=0.001). Overweight and obese children had a higher AGEs/sRAGE-ratio compared to lean controls, suggesting an obesity-related oxidative homeostasis dysregulation.
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