Multivariate analysis of metabolomic data to identify biological pathways modified by a clinical intervention

INTRODUCTION: High throughput metabolomic assays offer a huge opportunity to quantify the cellular processes underlying disease and intervention pathways. However, the multi-dimensional inter-relatedness between these processes coupled with the complex noisy measurement environment create a need for generation of new methods that move beyond simple pairwise associations. OBJECTIVES: To evaluate the utility of a simple, multivariate, relational comparison method called CLARITY in the context of metabolomics data. METHODS: Nuclear magnetic resonance (NMR)-derived metabolomics data collected from the same individuals (N = 125) before and after a weight management intervention in By-Band-Sleeve (BBS), a clinical trial of metabolic and bariatric surgery, were used. First a traditional (univariate) linear mixed model approach was taken to identify metabolites that were changed post-intervention. The CLARITY method was then used to generate a covariance-based relational anomaly score with a view to increasing classification performance of the underlying cause of changes to the levels of and covariances between metabolites. RESULTS: CLARITY enabled further characterisation of metabolites identified in univariate linear regression analyses, differentiating those that exhibited covariance changes from those with mean changes only. An additional cluster of metabolites were identified as undergoing a relational change that would not have been detected using traditional methods. CONCLUSIONS: Gathering insights about biological pathways from large-scale metabolomics data has the potential to inform the future design of modelling and laboratory experiments aimed at capturing the underlying biological processes relevant to disease.

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Publication Details

Journal
Metabolomics
Published
2026-07-27
DOI
https://doi.org/10.1007/s11306-026-02490-w
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Multivariate analysis of metabolomic data to identify biological pathways modified by a clinical intervention

Chris Rogers, Daniel J. Lawson, Jane Blazeby, Nicholas J. Timpson et al.
Metabolomics
Metabolomics and Mass Spectrometry Studies
article

Multivariate analysis of metabolomic data to identify biological pathways modified by a clinical intervention

Chris Rogers, Daniel J. Lawson, Jane Blazeby, Nicholas J. Timpson, Laura J. Corbin
article en

Abstract

INTRODUCTION: High throughput metabolomic assays offer a huge opportunity to quantify the cellular processes underlying disease and intervention pathways. However, the multi-dimensional inter-relatedness between these processes coupled with the complex noisy measurement environment create a need for generation of new methods that move beyond simple pairwise associations. OBJECTIVES: To evaluate the utility of a simple, multivariate, relational comparison method called CLARITY in the context of metabolomics data. METHODS: Nuclear magnetic resonance (NMR)-derived metabolomics data collected from the same individuals (N = 125) before and after a weight management intervention in By-Band-Sleeve (BBS), a clinical trial of metabolic and bariatric surgery, were used. First a traditional (univariate) linear mixed model approach was taken to identify metabolites that were changed post-intervention. The CLARITY method was then used to generate a covariance-based relational anomaly score with a view to increasing classification performance of the underlying cause of changes to the levels of and covariances between metabolites. RESULTS: CLARITY enabled further characterisation of metabolites identified in univariate linear regression analyses, differentiating those that exhibited covariance changes from those with mean changes only. An additional cluster of metabolites were identified as undergoing a relational change that would not have been detected using traditional methods. CONCLUSIONS: Gathering insights about biological pathways from large-scale metabolomics data has the potential to inform the future design of modelling and laboratory experiments aimed at capturing the underlying biological processes relevant to disease.

MetabolomicsVol. 22(4)
University Hospitals Bristol NHS Foundation Trust (GB), University of Bristol (GB), NIHR Bristol Biomedical Research Centre (GB), MRC Epidemiology Unit (GB), University Hospitals Bristol and Weston NHS Foundation Trust (GB)
Wellcome Trust, United Kingdom Clinical Research Collaboration, Cancer Research UK, National Institute for Health and Care Research, British Heart Foundation, Department of Health and Social Care, University of Bristol, Medical Research Council, Engineering and Physical Sciences Research Council, Health Technology Assessment Programme
Openalex Percentile: Top 99%
Metabolomics and Mass Spectrometry Studies
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