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Uncoupling protein gene UCP1-3826A/G, UCP2 Ins/Del and UCP3-55C/T polymorphisms in obese Turkish children
Hasibe Verdi1, Sibel Tulgar Kınık1, H Pınar Baysan-Çebi1
1Departments of Medical Biology, Başkent University Faculty of Medicine, Ankara.
Insights
Genetic variations in mitochondrial uncoupling proteins (UCP1, UCP2, UCP3) are not linked to childhood obesity in Turkish children. However, UCP2 gene variations may affect early insulin response after glucose intake.
Area of Science:
- Genetics
- Metabolism
- Pediatrics
Background:
- Mitochondrial uncoupling proteins (UCP) 1, 2, and 3 are key regulators of energy metabolism.
- Previous studies on UCP genotypes and obesity have yielded conflicting results.
- Investigating UCP gene polymorphisms in relation to obesity is crucial for understanding metabolic health.
Purpose of the Study:
- To examine the association between common UCP polymorphisms (UCP1-3826A/G, UCP2 Ins/Del, UCP3-55C/T) and obesity in Turkish children.
- To analyze the relationship of these UCP polymorphisms with metabolic parameters in obese children.
Main Methods:
- Genotyping of UCP1, UCP2, and UCP3 gene polymorphisms in 189 children (102 obese, 87 controls).
- Measurement of fasting lipid, glucose, and insulin levels in obese children.
- Oral glucose tolerance test (OGTT) with glucose and insulin level monitoring in 60 obese children.
Main Results:
- No significant differences in UCP polymorphism frequencies between obese and non-obese children.
- UCP1, UCP2, and UCP3 genotypes did not correlate with fasting metabolic parameters.
- UCP2 Insertion allele carriers showed significantly higher 30-minute insulin levels during OGTT.
Conclusions:
- UCP1-3826A/G, UCP2 Ins/Del, and UCP3-55C/T polymorphisms are not associated with obesity in Turkish children.
- The UCP2 Insertion allele may negatively impact early insulin response to glucose loading.
- Further research is needed to clarify the role of UCP2 in glucose metabolism and insulin sensitivity.
Background:
Mitochondrial uncoupling proteins (UCP) 1, 2 and 3 are members of the anion carrier protein family located in the inner mitochondrial membrane. There are various controversial reports on UCP genotypes and obesity in adults and children. This study aims to investigate the link between mostly studied UCP polymorphisms (UCP1-3826A/G, UCP2 Insertion/Deletion (Ins/Del) polymorphism of exon 8, and UCP3-55C/T Polymorphisms) and obesity in Turkish children. Furthermore, the relationships of UCP polymorphisms are also analyzed within the scope of metabolic parameters of obese children.
Methods:
Molecular screening of the UCP1, UCP2, and UCP3 gene polymorphisms was carried out in 189 children aged 6 to 18 years, 102 of who had exogenous obesity (54 girls) and 87 of whom were healthy controls (48 girls). In the obese group, fasting lipids, glucose and insulin levels were measured. In 60 obese children, an oral glucose tolerance test (OGTT) was performed with 0, 30, 60, 90 and 120 minutes of sampling for plasma glucose and insulin levels.
Results:
The frequency of UCP polymorphisms was similar in obese and non-obese children. In obese children, fasting lipids, glucose and insulin levels were not different among the UCP 1, 2 and 3 genotypes. While no relationship was found between the UCP 1 and 3 genotypes and glucose/insulin levels during OGTT, carriers of the Insertion allele with UCP2 Ins/Del polymorphism had significantly higher 30-minute insulin levels (p=0.018).
Conclusions:
Polymorphisms of the UCP1-3826A/G, UCP2 Ins/Del, and UCP3-55C/T are not associated with obesity and related pathologies in Turkish children. However, the presence of the Ins allele of the UCP2 gene has been found to have an unfavorable influence on early insulin excursion after glucose loading.
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