Publication:
Plasma Acylcarnitines and Risk of Type 2 Diabetes in a Mediterranean Population at High Cardiovascular Risk.

dc.contributor.authorGuasch-Ferré, Marta
dc.contributor.authorRuiz-Canela, Miguel
dc.contributor.authorLi, Jun
dc.contributor.authorZheng, Yan
dc.contributor.authorBulló, Mònica
dc.contributor.authorWang, Dong D
dc.contributor.authorToledo, Estefanía
dc.contributor.authorClish, Clary
dc.contributor.authorCorella, Dolores
dc.contributor.authorEstruch, Ramon
dc.contributor.authorRos, Emilio
dc.contributor.authorFitó, Montserrat
dc.contributor.authorArós, Fernando
dc.contributor.authorFiol, Miquel
dc.contributor.authorLapetra, José
dc.contributor.authorSerra-Majem, Lluís
dc.contributor.authorLiang, Liming
dc.contributor.authorPapandreou, Christopher
dc.contributor.authorDennis, Courtney
dc.contributor.authorMartínez-González, Miguel A
dc.contributor.authorHu, Frank B
dc.contributor.authorSalas-Salvadó, Jordi
dc.date.accessioned2023-01-25T10:24:21Z
dc.date.available2023-01-25T10:24:21Z
dc.date.issued2019
dc.description.abstractThe potential associations between acylcarnitine profiles and incidence of type 2 diabetes (T2D) and whether acylcarnitines can be used to improve diabetes prediction remain unclear. To evaluate the associations between baseline and 1-year changes in acylcarnitines and their diabetes predictive ability beyond traditional risk factors. We designed a case-cohort study within the PREDIMED Study including all incident cases of T2D (n = 251) and 694 randomly selected participants at baseline (follow-up, 3.8 years). Plasma acylcarnitines were measured using a targeted approach by liquid chromatography-tandem mass spectrometry. We tested the associations between baseline and 1-year changes in individual acylcarnitines and T2D risk using weighted Cox regression models. We used elastic net regressions to select acylcarnitines for T2D prediction and compute a weighted score using a cross-validation approach. An acylcarnitine profile, especially including short- and long-chain acylcarnitines, was significantly associated with a higher risk of T2D independent of traditional risk factors. The relative risks of T2D per SD increment of the predictive model scores were 4.03 (95% CI, 3.00 to 5.42; P An acylcarnitine profile, mainly including short- and long-chain acylcarnitines, was significantly associated with higher T2D risk in participants at high cardiovascular risk. The inclusion of acylcarnitines into the model did not significantly improve the T2D prediction C-statistics beyond traditional risk factors, including fasting glucose.
dc.identifier.doi10.1210/jc.2018-01000
dc.identifier.essn1945-7197
dc.identifier.pmcPMC6435097
dc.identifier.pmid30423132
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435097/pdf
dc.identifier.unpaywallURLhttps://academic.oup.com/jcem/article-pdf/104/5/1508/28224388/jc.2018-01000.pdf
dc.identifier.urihttp://hdl.handle.net/10668/13180
dc.issue.number5
dc.journal.titleThe Journal of clinical endocrinology and metabolism
dc.journal.titleabbreviationJ Clin Endocrinol Metab
dc.language.isoen
dc.organizationSevilla
dc.page.number1508-1519
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, N.I.H., Extramural
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshBiomarkers
dc.subject.meshCardiovascular Diseases
dc.subject.meshCarnitine
dc.subject.meshCase-Control Studies
dc.subject.meshDiabetes Mellitus, Type 2
dc.subject.meshDiet, Mediterranean
dc.subject.meshFemale
dc.subject.meshFollow-Up Studies
dc.subject.meshHumans
dc.subject.meshIncidence
dc.subject.meshMale
dc.subject.meshMetabolomics
dc.subject.meshMiddle Aged
dc.subject.meshPrognosis
dc.subject.meshProspective Studies
dc.subject.meshROC Curve
dc.subject.meshRisk Factors
dc.titlePlasma Acylcarnitines and Risk of Type 2 Diabetes in a Mediterranean Population at High Cardiovascular Risk.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number104
dspace.entity.typePublication

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