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Published on: June 3, 2016
ADIPOQ Genotypes, Adiponectin Isoforms, and Hypertension Risk in Pediatric Obesity
Huemara Yuri Almeida1, Warlley Rosa Cunha2, Carla Márcia Moreira Lanna3
1School of Pharmacy, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.
Insights
ADIPOQ gene variants significantly impact high molecular weight adiponectin (HMW APN) levels and hypertension risk in obese children. These findings suggest potential early biomarkers for cardiometabolic risk.
Area of Science:
- Genetics and Molecular Biology
- Pediatric Endocrinology
- Cardiovascular Health
Background:
- Adiponectin (APN), particularly its high molecular weight (HMW) isoform, plays a crucial role in metabolic regulation and cardiovascular protection.
- Genetic variations in the ADIPOQ gene, such as rs.266729 and rs.1501299, are implicated in influencing APN levels and are linked to obesity-related hypertension.
Purpose of the Study:
- To investigate the impact of ADIPOQ polymorphisms on plasma levels of total APN, HMW APN, and the HMW/APN ratio.
- To assess the association between these ADIPOQ polymorphisms and hypertension risk in a pediatric population with obesity.
Main Methods:
- A study involving 297 participants aged 5-18 years, including healthy controls, normotensive obese children, and obese children with hypertension.
- Plasma APN and HMW levels were quantified using ELISA, and genotyping for ADIPOQ variants (rs.266729 and rs.1501299) was performed.
- Multivariate regression and haplotype analyses were employed to evaluate associations with phenotypic traits and hypertension risk.
Main Results:
- The CG genotype of rs.266729 was linked to reduced HMW levels and HMW/APN ratio.
- The GT genotype of rs.1501299 was associated with elevated HMW levels and HMW/APN ratio, and showed a trend towards lower hypertension risk.
- Specific ADIPOQ haplotypes ('G,G' and 'C,G') demonstrated significant associations with APN/HMW levels and hypertension risk.
Conclusions:
- ADIPOQ gene polymorphisms and haplotypes significantly influence HMW adiponectin levels in obese children and adolescents.
- These genetic factors play a role in modulating hypertension risk within this pediatric population.
- The findings highlight the potential of ADIPOQ variants as early biomarkers for identifying cardiometabolic risk in children with obesity.
Background:
Adiponectin (APN), especially its high molecular weight (HMW) isoform, is essential for metabolic regulation and cardiovascular protection. Variants in the ADIPOQ gene, including rs.266729 and rs.1501299, may influence APN levels and have been associated with obesity-related hypertension.
Aims:
To evaluate the effects of ADIPOQ polymorphisms on plasma levels of total APN, the HMW isoform, and the HMW/APN ratio, as well as their association with hypertension in children and adolescents with obesity.
Methods:
We studied 297 participants aged 5-18 years: healthy controls (n = 142), normotensive children with obesity (n = 104), and children with obesity and hypertension (n = 51). Plasma APN and HMW levels were measured by ELISA. Genotyping for rs.266729 and rs.1501299 was performed using TaqMan assays. Associations with phenotype and hypertension risk were evaluated using multivariate linear and logistic regression, including haplotype analysis.
Results:
The CG genotype of rs.266729 was associated with lower HMW levels (β = -0.50; p = 0.02) and HMW/APN ratio (β = -0.02; p = 0.04). The GT genotype of rs.1501299 was associated with increased HMW levels (β = 0.70; p = 0.001) and the HMW/APN ratio (β = 0.02; p = 0.04). A trend toward a significant association with lower hypertension risk was observed for the dominant model (GT+TT vs. GG) of rs.1501299 (OR = 0.49, p = 0.05). The 'G,G' haplotype exhibited a negative synergistic effect on APN and HMW. In contrast, the 'C,G' haplotype was associated with an increased risk of hypertension compared to the CT reference haplotype (OR = 2.05; p = 0.02).
Conclusions:
ADIPOQ polymorphisms and haplotypes significantly modulate HMW adiponectin levels and influence hypertension risk in pediatric obesity, supporting their potential utility as early biomarkers for cardiometabolic risk.
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