Insulin sensitivity was strongly positively correlated with IGFBP-I levels (r = 0.65, P < 0.0001), while fasting insulin and BMI showed inverse correlations.
Cross-Sectional (n=104)
In healthy pubertal children, insulin sensitivity, obesity, and IGF-I are important predictors of IGFBP-I levels.
Effect estimate: r = 0.65
p-value: p=< 0.0001
In conditions associated with insulin resistance, insulin-like growth factor binding protein-I (IGFBP-I) levels have been shown to correlate inversely with insulin levels. Puberty is associated with insulin resistance and thus provides a model for comparing the relationship of IGFBP-I to both insulin levels and measures of insulin sensitivity. Our study population consisted of 104 healthy pubertal children, age 9.8-14.6 yr. Each subject had his/her insulin sensitivity (Si) assessed by the modified minimal model of Bergman, which employs a frequently sampled i.v. glucose tolerance test. Results showed that IGFBP-I levels were significantly higher in boys than in pubertally matched girls (P < 0.01). There was a strong positive correlation between IGFBP-I levels and Si (r = 0.65, P < 0.0001) and a weaker negative correlation with fasting insulin levels (r = -0.38, P < 0.0001). An inverse relationship was also found between IGFBP-I levels and body mass index (r = -0.46, P < 0.0001) and with IGF-I levels (girls only, r = -0.41, P < 0.003). Consequently, insulin sensitivity, obesity, and IGF-I are important predictors of IGFBP-I levels in pubertal children. It is possible that insulin-mediated suppression of IGFBP-I in obese children may increase free IGF-I levels and thus contribute to somatic growth. The same mechanism may operate in pubertal children, where insulin resistance and growth acceleration occur simultaneously.
Travers et al. (Mon,) conducted a cross-sectional in Healthy pubertal children (n=104). Insulin sensitivity and obesity was evaluated on Correlation between IGFBP-I levels and insulin sensitivity (Si) (r = 0.65, p=< 0.0001). Insulin sensitivity was strongly positively correlated with IGFBP-I levels (r = 0.65, P < 0.0001), while fasting insulin and BMI showed inverse correlations.