Abstract

Objective: Osteocalcin has been shown to exert an endocrine influence on bone and energy metabolism in both animals and humans; recent evidence indicating a regulatory role for osteocalcin in glucose homeostasis and energy metabolism and as a marker for bone metabolism. The aim of this study was to investigate the interaction between osteocalcin, body composition, and blood biomarkers in men with spinal cord injury (SCI) compared with able-bodied male controls. Materials and Methods: Twenty men with SCI were matched for age, height, and weight with 20 able-bodied controls. Body composition, bone density and blood levels of adiponectin, leptin, insulin, glucose, insulin-like growth factor-1 (IGF-1) were undertaken. Total body and regional fat mass (FM), fat free mass (FFM), total body bone mineral density (BMD) and circulating levels of blood biomarkers were compared between the two groups and correlation analyses performed between osteocalcin and all measures. Results: Compared with controls, SCI had lower total and leg FFM (P<0.05), but higher total and regional FM (P<0.05). Osteocalcin negatively correlated with age (P<0.05), and positively with total, trunk and arm FFM, and IGF-1 (P<0.05) in SCI men. Negative correlations between osteocalcin and age (P<0.05) and positive correlations with total and all regional FM depots, leptin, fasting glucose, and IGF-1 (P<0.05) were found for the controls. Conclusions: Crosstalk between fat mass, osteocalcin, glucose metabolism and adipokines is lost with decentralisation in the sympathetic nervous system (SNS). The clinical impact of this decentralisation deserves further investigation. These findings do not imply causality, but should be considered hypothesis generating.

Highlights

  • The skeleton has many functions within the human body

  • Osteocalcin negatively correlated with age (P

  • Crosstalk between fat mass, osteocalcin, glucose metabolism and adipokines is lost with decentralisation in the sympathetic nervous system (SNS)

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Summary

Introduction

The skeleton has many functions within the human body Recent research brings this organ system, like that of adipose tissue, to the fore in key areas of metabolic regulation. Muscle-secreted myokines have been identified as active regulators of metabolic function [7,8,9]. Key components of this metabolic control are the bone-derived osteokines, osteocalcin, adipose tissue-derived adipokines, leptin and adiponectin, and the sympathetic nervous system (SNS) [1,10,11]. Osteocalcin acts directly on the pancreas to increase insulin sensitivity and β-cell proliferation, and indirectly through adiponectin, to improve insulin

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