Abstract

BackgroundThe directional influences between serum sex hormone-binding globulin (SHBG), adiposity and insulin resistance during pubertal growth remain unclear. The aim of this study was to investigate bidirectional associations between SHBG and insulin resistance (HOMA-IR) and adiposity from childhood to early adulthood.MethodsParticipants were 396 healthy girls measured at baseline (age 11.2 years) and at 1, 2, 4 and 7.5 years. Serum concentrations of estradiol, testosterone and SHBG were determined by ELISA, glucose and insulin by enzymatic photometry, insulin-like growth factor 1 (IGF-1) by time-resolved fluoroimmunoassays, whole-body fat mass by dual-energy X-ray absorptiometry and HOMA-IR were determined by homeostatic model assessment. The associations were examined using cross-lagged path models.ResultsIn a cross-lagged path model, SHBG predicted HOMA-IR before menarche β = −0.320 (95% CI: −0.552 to −0.089), P = 0.007, independent of adiposity and IGF-1. After menarche, no directional effect was found between SHBG and insulin resistance or adiposity.ConclusionsOur results suggest that in early puberty, decline in SHBG predicts development of insulin resistance, independent of adiposity. However, after menarche, no directional influences between SHBG, adiposity and insulin resistance were found, suggesting that observational associations between SHBG, adiposity and insulin resistance in pubertal children may be subject to confounding. Further research is needed to understand the underlying mechanisms of the associations between SHBG and cardiometabolic risk markers in peripubertal children.

Highlights

  • Sex steroids are important regulators of pubertal development and their biological action is governed by sex hormone-binding globulin (SHBG) (1)

  • Low serum SHBG level has been associated with increased adiposity and insulin resistance in children and adolescents (3, 8, 9, 10, 11, 12); it has been hypothesized that SHBG might be an important regulator of puberty and a biomarker for cardiometabolic risk (3)

  • We investigated bidirectional associations between serum SHBG, adiposity and insulin resistance at five time points in females transitioning from pre-puberty to early adulthood using a cross-lagged panel model analysis

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Summary

Introduction

Sex steroids are important regulators of pubertal development and their biological action is governed by sex hormone-binding globulin (SHBG) (1). Some of the variation in circulating SHBG might be related to body composition and insulin sensitivity, both of which change substantially during puberty (6, 7) Along these lines, low serum SHBG level has been associated with increased adiposity and insulin resistance in children and adolescents (3, 8, 9, 10, 11, 12); it has been hypothesized that SHBG might be an important regulator of puberty and a biomarker for cardiometabolic risk (3). The directional influences between serum sex hormone-binding globulin (SHBG), adiposity and insulin resistance during pubertal growth remain unclear. The aim of this study was to investigate bidirectional associations between SHBG and insulin resistance (HOMA-IR) and adiposity from childhood to early adulthood. Conclusions: Our results suggest that in early puberty, decline in SHBG predicts development of insulin resistance, independent of adiposity. Further research is needed to understand the underlying mechanisms of the associations between SHBG and cardiometabolic risk markers in peripubertal children

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