Abstract
Background: Metabolic profiling of biofluid specimens is an established method for investigating disease states in clinical studies but is only recently being applied to large-scale human population studies. As part of protocol development for the UK Biobank study, a 1H nuclear magnetic resonance (NMR)-based metabonomic analysis of specimen storage effects and analytical reproducibility was carried out using urine and serum specimens from 40 volunteers. Methods: Aliquots of each specimen were stored for t=0 and t=24 h at 4°C prior to freezing, and in the case of serum samples for a further 12 h (t=36), to determine whether the storage times affected specimen composition and quality. A blinded split-specimen matching exercise was implemented to assign candidate spectral pairs stored for different times using multivariate statistical analysis of the NMR data. Results: Using a chemometric strategy, split specimens at time t=0 and t=24 or 36 h after storage at 4°C were easily paired and the splitspecimen matching task was reduced to a workable size. 1H NMR profiling established that the t=24 h urine and serum groups showed no systematic metabolite changes, indicating biochemical stability. Some small differences in serum specimens stored for t=36 h at 4°C were detectable only by multivariate analysis, and were attributed to generalized alterations in proteins and protein fragments, and possibly trimethylamine-N-oxide. No other specific metabolite was implicated. Conclusions: For the purposes of NMR-based analysis, storage of urine and serum for up to t=24 h at 4°C does not detectably affect the metabolic profile and the methodology is robust. Future application of multivariate methods to data-rich studies should substantially enhance information recovery from epidemiological studies. © The Author 2008; all rights reserved.
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Barton, R. H., Nicholson, J. K., Elliott, P., & Holmes, E. (2008). High-throughput 1H NMR-based metabolic analysis of human serum and urine for large-scale epidemiological studies: Validation study. International Journal of Epidemiology, 37(SUPPL. 1). https://doi.org/10.1093/ije/dym284
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