A laboratory approach for characterizing chronic fatigue: what does metabolomics tell us?

Introduction Manifestations of fatigue range from chronic fatigue up to a severe syndrome and myalgic encephalomyelitis. Fatigue grossly affects the functional status and quality of life of affected individuals, prompting the World Health Organization to recognize it as a chronic non-communicable co...

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Veröffentlicht in:Metabolomics 2019-12, Vol.15 (12), p.158-11, Article 158
Hauptverfasser: Erasmus, Elardus, Mason, Shayne, van Reenen, Mari, Steffens, Francois E., Vorster, B. Chris, Reinecke, Carolus J.
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Sprache:eng
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Zusammenfassung:Introduction Manifestations of fatigue range from chronic fatigue up to a severe syndrome and myalgic encephalomyelitis. Fatigue grossly affects the functional status and quality of life of affected individuals, prompting the World Health Organization to recognize it as a chronic non-communicable condition. Objectives Here, we explore the potential of urinary metabolite information to complement clinical criteria of fatigue, providing an avenue towards an objective measure of fatigue in patients presenting with the full spectrum of fatigue levels. Methods The experimental group consisted of 578 chronic fatigue female patients. The measurement design was composed of (1) existing clinical fatigue scales, (2) a hepatic detoxification challenge test, and (3) untargeted proton nuclear magnetic resonance ( 1 H-NMR) procedure to generate metabolomics data. Data analysed via an in-house Matlab script that combines functions from a Statistics and a PLS Toolbox. Results Multivariate analysis of the original 459 profiled 1 H-NMR bins for the low (control) and high (patient) fatigue groups indicated complete separation following the detoxification experimental challenge. Important bins identified from the 1 H-NMR spectra provided quantitative metabolite information on the detoxification challenge for the fatigue groups. Conclusions Untargeted 1 H-NMR metabolomics proved its applicability as a global profiling tool to reveal the impact of toxicological interventions in chronic fatigue patients. No clear potential biomarker emerged from this study, but the quantitative profile of the phase II biotransformation products provide a practical visible effect directing to up-regulation of crucial phase II enzyme systems in the high fatigue group in response to a high xenobiotic-load.
ISSN:1573-3882
1573-3890
DOI:10.1007/s11306-019-1620-4