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Lysine pathway metabolites and the risk of type 2 diabetes and cardiovascular disease in the PREDIMED study: results from two case-cohort studies.
Razquin, Cristina; Ruiz-Canela, Miguel; Clish, Clary B; Li, Jun; Toledo, Estefania; Dennis, Courtney; Liang, Liming; Salas-Huetos, Albert; Pierce, Kerry A; Guasch-Ferré, Marta; Corella, Dolores; Ros, Emilio; Estruch, Ramon; Gómez-Gracia, Enrique; Fitó, Montse; Lapetra, Jose; Romaguera, Dora; Alonso-Gómez, Angel; Serra-Majem, Lluis; Salas-Salvadó, Jordi; Hu, Frank B; Martínez-González, Miguel A.
Afiliação
  • Razquin C; Department of Preventive Medicine and Public Health, University of Navarra, Pamplona, Spain.
  • Ruiz-Canela M; IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.
  • Clish CB; CIBER Fisiopatología de la Obesidad y Nutrición (CIBERObn), Instituto de Salud Carlos III, Madrid, Spain.
  • Li J; Department of Preventive Medicine and Public Health, University of Navarra, Pamplona, Spain.
  • Toledo E; IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.
  • Dennis C; CIBER Fisiopatología de la Obesidad y Nutrición (CIBERObn), Instituto de Salud Carlos III, Madrid, Spain.
  • Liang L; Broad Institute of MIT and Harvard University, Cambridge, USA.
  • Salas-Huetos A; Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Spain.
  • Pierce KA; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, USA.
  • Guasch-Ferré M; Department of Preventive Medicine and Public Health, University of Navarra, Pamplona, Spain.
  • Corella D; IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.
  • Ros E; CIBER Fisiopatología de la Obesidad y Nutrición (CIBERObn), Instituto de Salud Carlos III, Madrid, Spain.
  • Estruch R; Broad Institute of MIT and Harvard University, Cambridge, USA.
  • Gómez-Gracia E; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, USA.
  • Fitó M; Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, USA.
  • Lapetra J; CIBER Fisiopatología de la Obesidad y Nutrición (CIBERObn), Instituto de Salud Carlos III, Madrid, Spain.
  • Romaguera D; Human Nutrition Unit, Faculty of Medicine and Health Sciences, Institut d'Investigació Sanitària Pere Virgili, Rovira i Virgili University, Reus, Spain.
  • Alonso-Gómez A; Broad Institute of MIT and Harvard University, Cambridge, USA.
  • Serra-Majem L; Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Spain.
  • Salas-Salvadó J; Human Nutrition Unit, Faculty of Medicine and Health Sciences, Institut d'Investigació Sanitària Pere Virgili, Rovira i Virgili University, Reus, Spain.
  • Hu FB; CIBER Fisiopatología de la Obesidad y Nutrición (CIBERObn), Instituto de Salud Carlos III, Madrid, Spain.
  • Martínez-González MA; Department of Preventive Medicine, University of Valencia, Valencia, Spain.
Cardiovasc Diabetol ; 18(1): 151, 2019 11 13.
Article em En | MEDLINE | ID: mdl-31722714
ABSTRACT

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Pipecólicos / Doenças Cardiovasculares / Diabetes Mellitus Tipo 2 / Ácido 2-Aminoadípico / Lisina Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Pipecólicos / Doenças Cardiovasculares / Diabetes Mellitus Tipo 2 / Ácido 2-Aminoadípico / Lisina Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article