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A plasma fatty acid profile associated to type 2 diabetes development: from the CORDIOPREV study

PURPOSE: The prevalence of type 2 diabetes mellitus (T2DM) is increasing worldwide. For this reason, it is essential to identify biomarkers for the early detection of T2DM risk and/or for a better prognosis of T2DM. We aimed to identify a plasma fatty acid (FA) profile associated with T2DM developme...

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Detalles Bibliográficos
Autores principales: Villasanta-Gonzalez, Alejandro, Alcala-Diaz, Juan Francisco, Vals-Delgado, Cristina, Arenas, Antonio Pablo, Cardelo, Magdalena P., Romero-Cabrera, Juan Luis, Rodriguez-Cantalejo, Fernando, Delgado-Lista, Javier, Malagon, Maria M., Perez-Martinez, Pablo, Schulze, Matthias B., Camargo, Antonio, Lopez-Miranda, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854256/
https://www.ncbi.nlm.nih.gov/pubmed/34609622
http://dx.doi.org/10.1007/s00394-021-02676-z
Descripción
Sumario:PURPOSE: The prevalence of type 2 diabetes mellitus (T2DM) is increasing worldwide. For this reason, it is essential to identify biomarkers for the early detection of T2DM risk and/or for a better prognosis of T2DM. We aimed to identify a plasma fatty acid (FA) profile associated with T2DM development. METHODS: We included 462 coronary heart disease patients from the CORDIOPREV study without T2DM at baseline. Of these, 107 patients developed T2DM according to the American Diabetes Association (ADA) diagnosis criteria after a median follow-up of 60 months. We performed a random classification of patients in a training set, used to build a FA Score, and a Validation set, in which we tested the FA Score. RESULTS: FA selection with the highest prediction power was performed by random survival forest in the Training set, which yielded 4 out of the 24 FA: myristic, petroselinic, α-linolenic and arachidonic acids. We built a FA Score with the selected FA and observed that patients with a higher score presented a greater risk of T2DM development, with an HR of 3.15 (95% CI 2.04–3.37) in the Training set, and an HR of 2.14 (95% CI 1.50–2.84) in the Validation set, per standard deviation (SD) increase. Moreover, patients with a higher FA Score presented lower insulin sensitivity and higher hepatic insulin resistance (p < 0.05). CONCLUSION: Our results suggest that a detrimental FA plasma profile precedes the development of T2DM in patients with coronary heart disease, and that this FA profile can, therefore, be used as a predictive biomarker. CLINICAL TRIALS.GOV.IDENTIFIER: NCT00924937. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00394-021-02676-z.