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Sample Preparation to Bioinformatics Analysis of DNA Methylation: Association Strategy for Obesity and Related Trait Studies
Published on: May 6, 2022
Uncoupling protein-2 gene polymorphisms are associated with obesity in Hungarian children
K Csernus1, G Pauler, E Erhardt
1Department of Pediatrics, Medical Faculty, University of Pecs, Pecs, Hungary. cs-kata@freemail.hu
Insights
Genetic variations in the uncoupling protein 2 (UCP-2) gene are linked to childhood obesity risk. Specific UCP-2 gene polymorphisms may influence a child's propensity towards being overweight or obese.
Area of Science:
- Genetics
- Pediatrics
- Metabolism
Background:
- Childhood obesity is a growing public health concern.
- Genetic factors play a role in energy metabolism and obesity development.
- Identifying gene polymorphisms associated with obesity can inform prevention strategies.
Purpose of the Study:
- To investigate the frequency of common gene polymorphisms related to energy metabolism in children.
- To determine if these polymorphisms affect the risk of childhood obesity in a Hungarian cohort.
Main Methods:
- Genotyping was performed on 1,346 children (6-17 years old), including 709 overweight/obese and 637 normal weight.
- Polymorphisms analyzed included those in the β3-adrenoreceptor, uncoupling protein (UCP)-1, UCP-2, UCP-3, and peroxisome proliferator-activated receptor-γ genes.
- Statistical analysis, including multivariate regression, was used to assess associations with obesity risk.
Main Results:
- The UCP-2 -866 A variant was associated with a reduced odds ratio for obesity.
- Conversely, UCP-2 exon 8 insertion allele carriers had an increased odds ratio for obesity.
- No significant associations were found for other examined gene polymorphisms.
Conclusions:
- Common polymorphisms within the UCP-2 gene appear to influence the susceptibility to overweight and obesity in Hungarian children.
- These findings highlight the potential role of UCP-2 gene variants in pediatric obesity.
Aim:
To determine the frequency of common polymorphisms of genes associated with energy metabolism among normal weight and overweight/obese children to look for effects on childhood obesity.
Methods:
Among 709 overweight/obese and 637 normal weight children (age 6-17 years), anthropometric measurements were carried out and genotyping for the following gene polymorphisms: β3 -adrenoreceptor Trp64Arg, uncoupling protein (UCP) -1 -3826 A/G, UCP-2 -866 G/A and exon 8 del/ins, UCP-3 -55 C/T and peroxisome proliferator-activated receptor-γ Pro12Ala.
Results:
On multivariate regression analysis adjusted for age and gender heterozygosity and homozygosity for the UCP-2 -866 A variant was associated with an odds ratio (OR) for obesity of 0.69 (95% CI: 0.52-0.92; p = 0.013) and 0.50 (95% CI: 0.32-0.79; p = 0.003), respectively, compared with G/G homozygotes. Heterozygotes and homozygotes for the UCP-2 exon 8 ins allele had an OR for obesity of 1.66 (95% CI: 1.24-2.23; p = 0.001) and 2.12 (95% CI: 1.23-3.63; p = 0.006), respectively, compared with del/del homozygotes. There were no significant differences in obesity risk in association with the other examined gene polymorphisms.
Conclusion:
Common polymorphisms of the UCP-2 gene might influence the propensity to overweight/obesity in Hungarian children.
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