Retinol-binding protein 4 and insulin resistance are related to body fat in primary and secondary schoolchildren : the Ouro Preto study.
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Data
2014
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Purpose Evidence suggests that plasma retinol-binding
protein 4 (RBP4) and insulin resistance are related to body
fat (BF). We aimed to assess the relationship between
RBP4 and insulin resistance with obesity in a mixed (skin
color) cohort of the Brazilian population.
Methods A nested case–control study was conducted in
227 schoolchildren aged 7–14 years. Schoolchildren with a
high BF percentage (% BF, C 30 for girls and C 25 for
boys) were identified as the obese group (n = 137), and
those with lower values were identified as the non-obese
group (n = 90). Percentage of body fat (% BF) was
determined by tetrapolar bioimpedance (Quantum II, RJL
System), RBP4 by enzyme-linked immunosorbent assay
(Immunology Consultants Laboratory), plasma fasting
insulin by chemiluminescent immunoassay (Access
Immunoassay System) and insulin resistance by the
homeostasis model insulin resistance (IRHOMA) index.
Serum lipid profile and arterial blood pressure were
evaluated.
Results The significant independent risk factors associated
with obesity were as follows: male sex, increased
serum LDL-C, RBP4 and IRHOMA. Among children with
higher RBP4, the association with obesity increased significantly
(from 3.1 to 8.5) in the presence of insulin
resistance, when compared to higher RBP4 and non-insulin
resistance.
Conclusion IRHOMA and RBP4 showed significant associations
with obesity and traditional CVD risk factors.
They might therefore be used as a marker for CVD risk and
have clinical implications in the development of comorbidities
associated with obesity.
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Body fat, Insulin resistance
Citação
CASTRO, A. P. P. et al. Retinol-binding protein 4 and insulin resistance are related to body fat in primary and secondary schoolchildren: the Ouro Preto study. European Journal of Nutrition, v. 53, p. 433-440, 2014. Disponível em: <http://link.springer.com/article/10.1007%2Fs00394-013-0543-5>. Acesso em: 20 jan. 2017.