The effects of NAMPT haplotypes and metabolic risk factors on circulating visfatin/NAMPT levels in childhood obesity

被引:15
作者
Belo, V. A. [1 ]
Luizon, M. R. [1 ]
Lacchini, R. [1 ]
Miranda, J. A. [2 ]
Lanna, C. M. M. [3 ]
Souza-Costa, D. C. [1 ]
Tanus-Santos, J. E. [1 ]
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Pharmacol, BR-14049900 Sao Paulo, Brazil
[2] Univ Estadual Campinas, Fac Med Sci, Dept Pharmacol, Campinas, SP, Brazil
[3] Univ Fed Juiz de Fora, Dept Physiol, Juiz De Fora, Brazil
基金
巴西圣保罗研究基金会;
关键词
visfatin; childhood obesity; metabolic risk factors; haplotypes; HOMEOSTASIS MODEL ASSESSMENT; TYPE-2; DIABETES-MELLITUS; INSULIN-RESISTANCE; SERUM VISFATIN; GLUCOSE-METABOLISM; GENETIC-VARIATIONS; ADIPOSE-TISSUE; VISCERAL FAT; PLASMA; INFLAMMATION;
D O I
10.1038/ijo.2013.173
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE: Polymorphisms in the NAMPT gene, which encodes the adipocytokine visfatin/nicotinamide phosphorybosil transferase (NAMPT), affect the circulating visfatin/NAMPT levels and are associated with obesity and cardiovascular diseases. However, no study has tested the hypothesis that NAMPT haplotypes could affect visfatin/NAMPT levels in case of childhood obesity. We investigated the effects of traditional metabolic risk factors (MRFs) and NAMPT polymorphisms T/C (rs1319501) and A/G (rs3801266) or haplotypes on visfatin/NAMPT levels in obese children and adolescents, and whether NAMPT polymorphisms and/or haplotypes are associated with susceptibility to childhood obesity. METHODS: We studied 175 control, 99 obese and 82 obese with >= 3 MRFs children and adolescents. Genotypes were determined by a Taqman allele discrimination assay and real- time PCR. The plasma visfatin/NAMPT level was measured using an enzyme immunoassay. RESULTS: Obese children and adolescents with >= 3 MRFs had higher plasma visfatin/NAMPT levels in comparison with control children and adolescents (P < 0.05). Although positive associations were observed between visfatin/NAMPT and body mass index (rs = 0.157; P = 0.034) as well as visfatin/NAMPT and waist circumference (rs = 0.192; P = 0.011), visfatin/NAMPT and high- density lipoprotein cholesterol were inversely associated (rs = -0.162; P = 0.031). No significant differences in genotype, allele or haplotype frequency distributions for the studied polymorphisms were found when the three groups were compared. However, higher plasma visfatin/NAMPT levels were found in control and obese subjects carrying the GG genotype for the A/G (rs3801266) polymorphism (P < 0.05) but not in obese children with X3 MRFs. Moreover, control subjects carrying the 'T-G' haplotype showed higher plasma visfatin/NAMPT levels. NAMPT genotypes or haplotypes were not associated with childhood obesity. CONCLUSIONS: Obesity in children with >= 3 MRFs increases plasma visfatin/NAMPT levels, and this marker was associated with body mass index and waist circumference. The A/G polymorphism and NAMPT haplotypes affect plasma visfatin/NAMPT levels in controls but not in obese children with >= 3 MRFs. These results suggest that obesity and MRFs are more influential than genetic polymorphisms in the determination of visfatin/NAMPT levels in obese children. Further research is necessary to explain why the GG genotype is not associated with increased visfatin/NAMPT levels in obese children with >= 3 MRFs.
引用
收藏
页码:130 / 135
页数:6
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