Evidence map›Paper›PMID 34919182›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2021

Systems epidemiology of metabolomics measures reveals new relationships between lipoproteins and other small molecules.

Fotios Drenos

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

1 author.

Fotios DrenosDepartment of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, UB8 3PH, UK. fotios.drenos@brunel.ac.uk.ORCID 0000-0003-2469-5516

Funding

British Heart Foundation BHF-TURING-19/2/1008British Heart Foundation SP/07/008/24066British Heart Foundation SP/19/5/34806Medical Research Council G1001357Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009Wellcome TrustWellcome Trust 102215/2/13/2Wellcome Trust WT088806Wellcome Trust WT092830M
6 · The paper itself

Abstract

introductionThe study of lipoprotein metabolism at the population level can provide valuable information for the organisation of lipoprotein related processes in the body. To use this information towards interventional hypotheses generation and testing, we need to be able to identify the mechanistic connections among the large number of observed correlations between the measured components of the system.

objectivesTo use population level metabolomics information to gain insight on their biochemical networks and metabolism.

methodsGenetic and metabolomics information for 230 metabolic measures, predominately lipoprotein related, from a targeted nuclear magnetic resonance approach, in two samples of an established European cohort, totalling more than 9400 individuals analysed using phenotypic and genetic correlations, as well as Mendelian Randomisation.

resultsMore than 20,500 phenotypic correlations were identified in the data, with almost 2000 also showing evidence of strong genetic correlation. Mendelian randomisation, provided evidence for a causal effect between 9496 pairs of metabolic measures, mainly between lipoprotein traits. The results provide insights on the organisation of lipoproteins in three distinct classes, the heterogeneity between HDL particles, and the association, or lack of, between CLA, glycolysis markers, such as glucose and citrate, and glycoproteins with lipids subfractions. Two examples for the use of the approach in systems biology of lipoproteins are presented.

conclusionsGenetic variation can be used to infer the underlying mechanisms for the associations between lipoproteins for hypothesis generation and confirmation, and, together with biological information, to map complex biological processes.

Indexed as

LipoproteinsMetabolomicsBiomarkersHumansMagnetic Resonance SpectroscopyBiomarkersLipoproteinsALSPACCausalityGenetic correlationMendelian randomizationMetabolomicsSystems epidemiology

Identifiers

PMID34919182
PMCPMC8683390

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