ARTÍCULO

Lysine pathway metabolites and the risk of type 2 diabetes and cardiovascular disease in the PREDIMED study: results from two case-cohort studies

Autores: Razquin Burillo, Cristina; Ruiz-Canela, Miguel; Clish, C. B.; Li, J.; Toledo Atucha, Estefanía; Dennis, C.; Liang, L. M.; Salas-Huetos, A.; Pierce, K. A.; Guasch-Ferre, M.; Corella, D.; Ros, E.; Estruch, R.; Gomez-Gracia, E.; Fito, M.; Lapetra, J.; Romaguera, D.; Alonso-Gomez, A.; Serra-Majem, L.; Salas-Salvado, J.; Hu, F. B.; Martínez González, Miguel Ángel (Autor de correspondencia)
Título de la revista: CARDIOVASCULAR DIABETOLOGY
ISSN: 1475-2840
Volumen: 18
Número: 1
Páginas: 151
Fecha de publicación: 2019
Lugar: WOS
Resumen:
Background The pandemic of cardiovascular disease (CVD) and type 2 diabetes (T2D) requires the identification of new predictor biomarkers. Biomarkers potentially modifiable with lifestyle changes deserve a special interest. Our aims were to analyze: (a) The associations of lysine, 2-aminoadipic acid (2-AAA) or pipecolic acid with the risk of T2D or CVD in the PREDIMED trial; (b) the effect of the dietary intervention on 1-year changes in these metabolites, and (c) whether the Mediterranean diet (MedDiet) interventions can modify the effects of these metabolites on CVD or T2D risk. Methods Two unstratified case-cohort studies nested within the PREDIMED trial were used. For CVD analyses, we selected 696 non-cases and 221 incident CVD cases; for T2D, we included 610 non-cases and 243 type 2 diabetes incident cases. Metabolites were quantified using liquid chromatography-tandem mass spectrometry, at baseline and after 1-year of intervention. Results In weighted Cox regression models, we found that baseline lysine (HR+1 SD increase = 1.26; 95% CI 1.06-1.51) and 2-AAA (HR+1 SD increase = 1.28; 95% CI 1.05-1.55) were both associated with a higher risk of T2D, but not with CVD. A significant interaction (p = 0.032) between baseline lysine and T2D on the risk of CVD was observed: subjects with prevalent T2D and high levels of lysine exhibited the highest risk of CVD. The intervention with MedDiet did not have a significant effect on 1-year changes of the metabolites. Conclusions Our results provide an independent prospective replication of the association of 2-AAA with future risk of T2D. We show an association of lysine with subsequent CVD risk, which is apparently diabetes-dependent. No evidence of effects of MedDiet intervention on lysine, 2-AAA or pipecolic acid changes was found. Trial registration ISRCTN35739639; registration date: 05/10/2005; recruitment start date 01/10/2003