Key result
APLN T-1860C polymorphism linked to ~339% increased obesity risk in female children alongside lower apelin.
Why the study?
Childhood obesity is a global health crisis, and apelin modulates feeding behaviour and energy homeostasis, but its concentrations and related gene polymorphisms remained to be clarified in Thai children.
Are apelin concentrations and APLN T-1860C/APLNR G212A polymorphisms associated with obesity and cardiometabolic parameters in Thai children?
Case-Control (n=325)
Are apelin concentrations and APLN T-1860C/APLNR G212A polymorphisms associated with obesity and cardiometabolic parameters in Thai children?
Odds Ratio: 4.39 (95% CI 1.25–15.28)
p-value: p=<0.05
Lower apelin concentrations and the APLN T-1860C polymorphism are associated with obesity and adverse cardiometabolic parameters in Thai children, particularly females.
Lower apelin levels associate with obesity and cardiometabolic markers in Thai children; leaves open whether APLN T-1860C aids risk stratification in girls.
BACKGROUND: Childhood obesity represents a serious global health crisis. Apelin and its receptor system are widely distributed throughout the central nervous system and have been demonstrated to serve a role modulating feeding behaviour and energy homeostasis. The purposes of this study were to examine apelin concentrations and anthropometric-cardiometabolic parameters in obese and non-obese children and to identify associations of APLN T-1860C and APLNR G212A polymorphisms with apelin levels and obesity among Thai children. METHODS: This case-control study included an analysis of 325 Thai children: 198 children with obesity and 127 healthy non-obese children. Anthropometric-cardiometabolic variables and apelin concentration were measured. Genotyping of APLN T-1860C and APLNR G212A was performed using the polymerase chain reaction-restriction fragment length polymorphism technique. RESULTS: The obese group had significantly lower apelin and HDL-C levels but significantly higher triglycerides and glucose (TyG) index values, TG/HDL-C ratio and TC/HDL-C ratio than the non-obese group (p < 0.01). Apelin level was negatively correlated with body size phenotypes and cardiometabolic parameters (p < 0.05). The APLN T-1860C polymorphism (OR = 4.39, 95% CI = 1.25-15.28) and apelin concentration (OR = 0.45, 95% CI = 0.23-0.92) were significantly associated with obesity among female children (p < 0.05) only, after adjusting for potential covariates. However, the APLNR G212A polymorphism showed no significant relationship with apelin concentration or obesity. CONCLUSION: These findings in Thai children suggest that apelin concentrations are related to obesity and cardiometabolic parameters. Furthermore, the APLN T-1860C polymorphism may influence susceptibility to obesity among female children.
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Suriyaprom et al. (2020) conducted a case-control in Childhood Obesity (n=325). APLN T-1860C polymorphism vs. Wild-type genotype / Non-obese controls was evaluated on Obesity in female children (OR 4.39, 95% CI 1.25-15.28, p=<0.05). The APLN T-1860C polymorphism was significantly associated with an increased risk of obesity among female Thai children (OR 4.39), alongside lower circulating apelin concentrations.
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