Authors: Leonie Venter Zander Lindeque Peet Jansen van Rensburg Francois van der Westhuizen Izelle Smuts Roan Louw
Publish Date: 2014/06/01
Volume: 11, Issue: 1, Pages: 111-121
Abstract
Mitochondrial diseases are a heterogeneous group of disorders characterised by impaired mitochondrial oxidative phosphorylation system Most often for mitochondrial disease where no metabolic diagnostic biomarkers exist a deficiency is diagnosed after analysing the respiratory chain enzymes complexes IIV in affected tissues or by identifying one of an ever expanding number of DNA mutations This presents a great challenge to identify cases to undergo the invasive diagnostic procedures required An untargeted liquid chromatography mass spectrometry metabolomics approach was used to search for a metabolic biosignature that can distinguish respiratory chain deficient RCD patients from clinical controls CC A cohort of 37 ethnically diverse cases was used Sample preparation liquid chromatography timeofflight mass spectrometry methods and data processing methods were standardised Furthermore the developed methodology used reverse phase chromatography in conjunction with positive electrospray ionisation and hydrophilic interaction chromatography with negative electrospray ionisation Urine samples of 37 patients representing two different experimental groups were analysed The two experimental groups comprised of patients with confirmed RCDs and CC After a variety of data mining steps and statistical analyses a list of 12 features were compiled with the ability to distinguish between patients with RCDs and CC Although the features of the biosignature needs to be identified and the biosignature validated this study demonstrates the value of untargeted metabolomics to identify a metabolic biosignature to possibly be applied in the selection criteria for RCDs
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