Evidence map›Paper›PMID 42509364›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2026

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

Rachel M Wood, Laura J Corbin, Jane M Blazeby, Chris A Rogers, Nicholas J Timpson, Daniel J Lawson

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Rachel M Wood *School of Mathematics, University of Bristol, Woodland Road, Bristol, BS8 1UG, UK.
Laura J Corbin *Population Health Sciences, University of Bristol, First Floor, Augustine's Courtyard, Orchard Lane, Bristol, BS1 5DS, UK. laura.corbin@bristol.ac.uk.ORCID http://orcid.org/0000-0002-4032-9500
Jane M BlazebyPopulation Health Sciences and Bristol Biomedical Research Centre, University of Bristol, 5 Tyndall Avenue, Bristol, BS8 1UD, UK.
Chris A RogersBristol Medical School, University of Bristol, First Floor, 5 Tyndall Avenue, Bristol, BS8 1UD, UK.
Nicholas J TimpsonPopulation Health Sciences, University of Bristol, First Floor, Augustine's Courtyard, Orchard Lane, Bristol, BS1 5DS, UK.
Daniel J LawsonSchool of Mathematics, University of Bristol, Woodland Road, Bristol, BS8 1UG, UK.

Funding

Engineering and Physical Sciences Research Council EP/S023569/1Medical Research Council MC_UU_00032/1National Institute for Health and Care Research HTA 09/127/53Wellcome TrustWellcome Trust 202802/Z/16/Z
6 · The paper itself

Abstract

introductionHigh 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.

objectivesTo evaluate the utility of a simple, multivariate, relational comparison method called CLARITY in the context of metabolomics data.

methodsNuclear 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.

resultsCLARITY 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.

conclusionsGathering 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.

Indexed as

MetabolomicsBariatric SurgeryHumansMagnetic Resonance SpectroscopyMetabolomeMultivariate AnalysisCLARITYMetabolomicsMultivariateNetworkNMR

Identifiers

PMID42509364
PMCPMC13407567

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.