Key result
Plasma VEGF concentrations were significantly higher in obese subjects and positively correlated with BMI (r = 0.407, P = 0.010), independent of insulin sensitivity.
Why the study?
Does BMI correlate with circulating VEGF levels independent of insulin sensitivity in healthy young men?
Cross-Sectional (n=45)
No
Does BMI correlate with circulating VEGF levels independent of insulin sensitivity in healthy young men?
Effect estimate: r = 0.407
p-value: p=0.010
Circulating VEGF levels positively correlate with BMI in healthy young men independent of insulin sensitivity, suggesting a potential mechanism linking obesity to type 2 diabetes complications.
VEGF-BMI correlation in healthy men is hypothesis-generating; leaves open any causal or clinical role independent of insulin sensitivity.
BACKGROUND: This is the first study to experimentally explore the direct relationship between circulating VEGF levels and body mass index (BMI) as well as to unravel the role of insulin sensitivity in this context under standardized glucose clamp conditions as the methodical gold-standard. In order to control for known influencing factors such as gender, medication, and arterial hypertension, we examined a highly homogeneous group of young male subjects. Moreover, to encompass also subjects beyond the normal BMI range, low weight and obese participants were additionally included and stress hormones as a main regulator of VEGF were assessed. METHODOLOGY/PRINCIPAL FINDINGS: Under euglycemic clamp conditions, VEGF was measured in 15 normal weight (BMI 20-25 kg/m(2)), 15 low weight (BMI<20 kg/m(2)), and 15 obese (BMI>30 kg/m(2)) male subjects aged 18-30 years and the insulin sensitivity index (ISI) was calculated. Since stress axis activation promotes VEGF secretion, concentrations of ACTH, cortisol, and catecholamines were monitored. Despite of comparable ACTH (P = 0.145), cortisol (P = 0.840), and norepinephrine (P = 0.065) levels, VEGF concentrations differed significantly between BMI-groups (P = 0.008) with higher concentrations in obese subjects as compared to normal weight (P = 0.061) and low weight subjects (P = 0.002). Pearson's correlation analysis revealed a positive relationship between BMI and VEGF levels (r = 0.407; P = 0.010) but no correlation of VEGF with ISI (r = 0.224; P = 0.175). CONCLUSIONS/SIGNIFICANCE: Our data demonstrate a positive correlation between concentrations of circulating VEGF levels and BMI in healthy male subjects under highly controlled conditions. This relationship which is apparently disconnected from insulin sensitivity may be part of some pathogenetic mechanisms underlying obesity and type 2 diabetes.
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Loebig et al. (2010) conducted a cross-sectional in Healthy (varying BMI) (n=45). Body Mass Index (BMI) vs. Normal weight and low weight was evaluated on Plasma VEGF concentrations (r = 0.407, p=0.010). Plasma VEGF concentrations were significantly higher in obese subjects and positively correlated with BMI (r = 0.407, P = 0.010), independent of insulin sensitivity.
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