Abstract

The metabolic changes in serum during a sport program were explored using a metabonomic approach, based on proton nuclear magnetic resonance (1H-NMR) spectroscopy and anthropometry. The aim of this study was to classify two groups of female university students with body mass index over 25 kg/m², using multiple measured descriptors. The first group (n=16) underwent a complex and well programmed 18-week physical training courses, and the second group (n=8), which was our control group, did not participate in any training course. Our descriptors consist of anthropometric descriptors (including height, weight, circumferences of arm, waist, hip and thigh, lean body mass and fat mass percentiles). Serum levels of growth hormone, insulin, and insulin like growth factor-1 were measured. 1H-NMR spectra was obtained using a 500-MHz Bruker spectrometer and was calculated for certain chemical shift integrals using Chenomx software for all the individuals in both groups. These descriptors were measured both before and after the training program for the experimental group. In order to make a linear model between growth hormone (GH) and 1H-NMR matrix as a set of variables, initially by multiple linear regression (MLR) stepwise as the variable selection method, the most important descriptors were selected by MLR modeling approaches. The results obtained for R2 training and test show an agreement between experimental and theoretical GH values. By applying counter-propagation Artificial Neural Networks (CP-ANN) classification methods, we significantly separated our 1st group from the other one.  Key words: Physical activity, blood serum, nuclear magnetic resonance, multiple linear regressions, artificial neural network.

Highlights

  • Studying human metabolite variations caused by external factors like diet, drugs and physical activity is a subdivision of metabonomic, which is defined as the quantitative measurement of the dynamic multiparametric metabolic response of living systems to pathophysiological stimuli or genetic modification (Gavaghan et al, 2000)

  • Nuclear magnetic resonance (NMR) spectroscopy has emerged as a key tool for understanding metabolic processes in living systems (Brown et al, 1977)

  • The range of spectroscopic techniques that are used in metabonomics are often so-called ‘hyphenated’ mode (e.g. liquid chromatography/ nuclear magnetic resonance/ mass spectrometry (LC–NMR–MS)

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Summary

Introduction

Studying human metabolite variations caused by external factors like diet, drugs and physical activity is a subdivision of metabonomic, which is defined as the quantitative measurement of the dynamic multiparametric metabolic response of living systems to pathophysiological stimuli or genetic modification (Gavaghan et al, 2000). The proton nuclear magnetic resonance (1H-NMR) spectroscopy of biofluids (urine, serum/plasma) and tissue generates comprehensive biochemical profiles of low molecular weight endogenous metabolites (Solanky et al, 2003). Nuclear magnetic resonance (NMR) spectroscopy has emerged as a key tool for understanding metabolic processes in living systems (Brown et al, 1977). The range of spectroscopic techniques that are used in metabonomics are often so-called ‘hyphenated’ mode (e.g. liquid chromatography/ nuclear magnetic resonance/ mass spectrometry (LC–NMR–MS).

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