Plasma acylcarnitines and risk of type 2 diabetes in a mediterranean population at high cardiovascular risk

Research output: Contribution to journalJournal articleResearchpeer-review

  • Miguel Ruiz-Canela
  • Jun Li
  • Yan Zheng
  • Mònica Bulló
  • Dong D. Wang
  • Estefanía Toledo
  • Clary Clish
  • Dolores Corella
  • Ramon Estruch
  • Emilio Ros
  • Montserrat Fitó
  • Fernando Arós
  • Miquel Fiol
  • José Lapetra
  • Llúis Serra-Majem
  • Liming Liang
  • Christopher Papandreou
  • Courtney Dennis
  • Miguel A. Martínez-González
  • Frank B. Hu
  • Jordi Salas-Salvadó

Context: The potential associations between acylcarnitine profiles and incidence of type 2 diabetes (T2D) and whether acylcarnitines can be used to improve diabetes prediction remain unclear. Objective: To evaluate the associations between baseline and 1-year changes in acylcarnitines and their diabetes predictive ability beyond traditional risk factors. Design, Setting, and Participants: 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. Results: 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 < 0.001) for the conventional model and 4.85 (95% CI, 3.65 to 6.45; P <0.001) for the model including acylcarnitines, with a hazard ratio of 1.33 (95% CI, 1.08 to 1.63; P < 0.001) attributed to the acylcarnitines. Including the acylcarnitines into the model did not significantly improve the area under the receiver operator characteristic curve (0.86 to 0.88, P = 0.61). A 1-year increase in C4OHcarnitine was associated with higher risk of T2D [per SD increment, 1.44 (1.03 to 2.01)]. Conclusions: 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.

Original languageEnglish
JournalJournal of Clinical Endocrinology and Metabolism
Volume104
Issue number5
Pages (from-to)1508-1519
Number of pages12
ISSN0021-972X
DOIs
Publication statusPublished - 2019
Externally publishedYes

Bibliographical note

Publisher Copyright:
Copyright © 2019 Endocrine Society.

ID: 358089821