Abstract
Metabolomic studies with a time-series design are widely used for discovery and validation of biomarkers. In such studies, changes of metabolic profiles over time under different conditions (e.g., control and intervention) are compared, and metabolites responding differently between the conditions are identified as putative biomarkers. To incorporate time-series information into the variable (biomarker) selection in partial least squares regression (PLS) models, we created PLS models with different combinations of bilinear/trilinear X and group/time response dummy Y. In total, five PLS models were evaluated on two real datasets, and also on simulated datasets with varying characteristics (number of subjects, number of variables, inter-individual variability, intra-individual variability and number of time points). Variables showing specific temporal patterns observed visually and determined statistically were labelled as discriminating variables. Bootstrapped-VIP scores were calculated for variable selection and the variable selection performance of five PLS models were assessed based on their capacity to correctly select the discriminating variables. The results showed that the bilinear PLS model with group × time response as dummy Y provided the highest recall (true positive rate) of 83–95% with high precision, independent of most characteristics of the datasets. Trilinear PLS models tend to select a small number of variables with high precision but relatively high false negative rate (lower power). They are also less affected by the noise compared to bilinear PLS models. In datasets with high inter-individual variability, bilinear PLS models tend to provide higher recall while trilinear models tend to provide higher precision. Overall, we recommend bilinear PLS with group x time response Y for variable selection applications in metabolomics intervention time series studies.
Highlights
Metabolomics is a widely applied technology for capturing the perturbations of metabolites in biological systems and for discovery of dietary and health biomarkers
“unknown” metabolome; extraction of information from raw analytical data; statistical analysis to select putative biomarkers with the capacity to discriminate the samples from different conditions; and further studies to validate the performance of selected biomarkers [3]
For both simulated and real data, a single cross validation scheme was implemented, and the optimal number of latent variables was decided as the smallest number at which the decrease in root mean squared error in cross validation (RMSECV) between consecutive models was less than 2%
Summary
Metabolomics is a widely applied technology for capturing the perturbations of metabolites in biological systems and for discovery of dietary and health biomarkers. Mass spectrometry (LC-MS), nuclear magnetic resonance spectroscopy (NMR), and gas chromatography–mass spectrometry (GC-MS) are most commonly employed in metabolomics studies providing information-rich, high throughput data [1]. Such data contains information on hundreds or even thousands of metabolites, resulting in challenges for both data pre-processing and statistical analysis [2]. Time-series design has been adopted in many metabolomic studies for both biomarker discovery and validation stages It is advantageous because it allows discovery of biomarkers responding to an intervention and provides time response information of biomarkers, which is of importance to select the best time window for sampling [5].
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