Institut Català de la Salut
[Hernandez Baixauli J] Eurecat, Centre Tecnològic de Catalunya, Unitat de Nutrició i Salut, Reus, Spain. Laboratori de Metabolisme i Obesitat, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Chomiciute G, Alcaide-Hidalgo JM, Crescenti A, Baselga-Escudero L] Eurecat, Centre Tecnològic de Catalunya, Unitat de Nutrició i Salut, Reus, Spain. [Palacios Jordan H] Eurecat, Centre Tecnològic de Catalunya, Centre for Omic Sciences (COS), Joint Unit Universitat Rovira i Virgili−EURECAT, Reus, Spain
Vall d'Hebron Barcelona Hospital Campus
2024-01-16T08:02:31Z
2024-01-16T08:02:31Z
2023-12-19
Hypertriglyceridemia; Inhibiting lipoprotein lipase
Hipertrigliceridèmia; Inhibició de la lipoproteïna lipasa
Hipertrigliceridemia; Inhibición de la lipoproteína lipasa
Hypertriglyceridemia (HTG) is an independent risk factor for atherosclerotic cardiovascular disease (ASCVD). One of the multiple origins of HTG alteration is impaired lipoprotein lipase (LPL) activity, which is an emerging target for HTG treatment. We hypothesised that early, even mild, alterations in LPL activity might result in an identifiable metabolomic signature. The aim of the present study was to assess whether a metabolic signature of altered LPL activity in a preclinical model can be identified in humans. A preclinical LPL-dependent model of HTG was developed using a single intraperitoneal injection of poloxamer 407 (P407) in male Wistar rats. A rat metabolomics signature was identified, which led to a predictive model developed using machine learning techniques. The predictive model was applied to 140 humans classified according to clinical guidelines as (1) normal, less than 1.7 mmol/L; (2) risk of HTG, above 1.7 mmol/L. Injection of P407 in rats induced HTG by effectively inhibiting plasma LPL activity. Significantly responsive metabolites (i.e. specific triacylglycerols, diacylglycerols, phosphatidylcholines, cholesterol esters and lysophospholipids) were used to generate a predictive model. Healthy human volunteers with the impaired predictive LPL signature had statistically higher levels of TG, TC, LDL and APOB than those without the impaired LPL signature. The application of predictive metabolomic models based on mechanistic preclinical research may be considered as a strategy to stratify subjects with HTG of different origins. This approach may be of interest for precision medicine and nutritional approaches.
This research was financially supported by the Catalan Government through the funding grant ACCIÓ-Eurecat (PRIV2019-PREVENTOMICS) and by the Centre for the Development of Industrial Technology (CDTI) of the Spanish Ministry of Science and Innovation under grant agreement: TECNOMIFOOD project. CER-20191010.
Article
Published version
English
Sistema cardiovascular - Malalties; Lipoproteïnalipasa - Inhibidors; Hipertriacilgliceridèmia - Factors de risc; DISEASES::Nutritional and Metabolic Diseases::Metabolic Diseases::Lipid Metabolism Disorders::Dyslipidemias::Hyperlipidemias::Hypertriglyceridemia; CHEMICALS AND DRUGS::Enzymes and Coenzymes::Enzymes::Hydrolases::Esterases::Carboxylic Ester Hydrolases::Lipoprotein Lipase; Other subheadings::Other subheadings::Other subheadings::/antagonists & inhibitors; DISEASES::Cardiovascular Diseases; ENFERMEDADES::enfermedades nutricionales y metabólicas::enfermedades metabólicas::trastornos del metabolismo de los lípidos::dislipidemias::hiperlipidemias::hipertrigliceridemia; COMPUESTOS QUÍMICOS Y DROGAS::enzimas y coenzimas::enzimas::hidrolasas::esterasas::éster carboxílico hidrolasas::lipoproteína lipasa; Otros calificadores::Otros calificadores::Otros calificadores::/antagonistas & inhibidores; ENFERMEDADES::enfermedades cardiovasculares
Nature Portfolio
Scientific Reports;13
https://doi.org/10.1038/s41598-023-49277-w
Attribution 4.0 International
http://creativecommons.org/licenses/by/4.0/
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