Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease. / García-Gavilán, Jesús F.; Babio, Nancy; Toledo, Estefanía; Semnani-Azad, Zhila; Razquin, Cristina; Dennis, Courtney; Deik, Amy; Corella, Dolores; Estruch, Ramón; Ros, Emilio; Fitó, Montserrat; Arós, Fernando; Fiol, Miquel; Lapetra, José; Lamuela-Raventos, Rosa; Clish, Clary; Ruiz-Canela, Miguel; Martínez-González, Miguel Ángel; Hu, Frank; Salas-Salvadó, Jordi; Guasch-Ferré, Marta.

In: Cardiovascular Diabetology, Vol. 22, No. 1, 340, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

García-Gavilán, JF, Babio, N, Toledo, E, Semnani-Azad, Z, Razquin, C, Dennis, C, Deik, A, Corella, D, Estruch, R, Ros, E, Fitó, M, Arós, F, Fiol, M, Lapetra, J, Lamuela-Raventos, R, Clish, C, Ruiz-Canela, M, Martínez-González, MÁ, Hu, F, Salas-Salvadó, J & Guasch-Ferré, M 2023, 'Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease', Cardiovascular Diabetology, vol. 22, no. 1, 340. https://doi.org/10.1186/s12933-023-02066-1

APA

García-Gavilán, J. F., Babio, N., Toledo, E., Semnani-Azad, Z., Razquin, C., Dennis, C., Deik, A., Corella, D., Estruch, R., Ros, E., Fitó, M., Arós, F., Fiol, M., Lapetra, J., Lamuela-Raventos, R., Clish, C., Ruiz-Canela, M., Martínez-González, M. Á., Hu, F., ... Guasch-Ferré, M. (2023). Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease. Cardiovascular Diabetology, 22(1), [340]. https://doi.org/10.1186/s12933-023-02066-1

Vancouver

García-Gavilán JF, Babio N, Toledo E, Semnani-Azad Z, Razquin C, Dennis C et al. Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease. Cardiovascular Diabetology. 2023;22(1). 340. https://doi.org/10.1186/s12933-023-02066-1

Author

García-Gavilán, Jesús F. ; Babio, Nancy ; Toledo, Estefanía ; Semnani-Azad, Zhila ; Razquin, Cristina ; Dennis, Courtney ; Deik, Amy ; Corella, Dolores ; Estruch, Ramón ; Ros, Emilio ; Fitó, Montserrat ; Arós, Fernando ; Fiol, Miquel ; Lapetra, José ; Lamuela-Raventos, Rosa ; Clish, Clary ; Ruiz-Canela, Miguel ; Martínez-González, Miguel Ángel ; Hu, Frank ; Salas-Salvadó, Jordi ; Guasch-Ferré, Marta. / Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease. In: Cardiovascular Diabetology. 2023 ; Vol. 22, No. 1.

Bibtex

@article{506bb5766074479faab5322e7b34903b,
title = "Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease",
abstract = "Background: Olive oil consumption has been inversely associated with the risk of type 2 diabetes (T2D) and cardiovascular disease (CVD). However, the impact of olive oil consumption on plasma metabolites remains poorly understood. This study aims to identify plasma metabolites related to total and specific types of olive oil consumption, and to assess the prospective associations of the identified multi-metabolite profiles with the risk of T2D and CVD. Methods: The discovery population included 1837 participants at high cardiovascular risk from the PREvenci{\'o}n con DIeta MEDiterr{\'a}nea (PREDIMED) trial with available metabolomics data at baseline. Olive oil consumption was determined through food-frequency questionnaires (FFQ) and adjusted for total energy. A total of 1522 participants also had available metabolomics data at year 1 and were used as the internal validation sample. Plasma metabolomics analyses were performed using LC–MS. Cross-sectional associations between 385 known candidate metabolites and olive oil consumption were assessed using elastic net regression analysis. A 10-cross-validation (CV) procedure was used, and Pearson correlation coefficients were assessed between metabolite-weighted models and FFQ-derived olive oil consumption in each pair of training–validation data sets within the discovery sample. We further estimated the prospective associations of the identified plasma multi-metabolite profile with incident T2D and CVD using multivariable Cox regression models. Results: We identified a metabolomic signature for the consumption of total olive oil (with 74 metabolites), VOO (with 78 metabolites), and COO (with 17 metabolites), including several lipids, acylcarnitines, and amino acids. 10-CV Pearson correlation coefficients between total olive oil consumption derived from FFQs and the multi-metabolite profile were 0.40 (95% CI 0.37, 0.44) and 0.27 (95% CI 0.22, 0.31) for the discovery and validation sample, respectively. We identified several overlapping and distinct metabolites according to the type of olive oil consumed. The baseline metabolite profiles of total and extra virgin olive oil were inversely associated with CVD incidence (HR per 1SD: 0.79; 95% CI 0.67, 0.92 for total olive oil and 0.70; 0.59, 0.83 for extra virgin olive oil) after adjustment for confounders. However, no significant associations were observed between these metabolite profiles and T2D incidence. Conclusions: This study reveals a panel of plasma metabolites linked to the consumption of total and specific types of olive oil. The metabolite profiles of total olive oil consumption and extra virgin olive oil were associated with a decreased risk of incident CVD in a high cardiovascular-risk Mediterranean population, though no associations were observed with T2D incidence. Trial registration : The PREDIMED trial was registered at ISRCTN (http://www.isrctn.com/ , ISRCTN35739639).",
keywords = "Cardiovascular disease, Metabolomics, Olive oil, Type 2 diabetes",
author = "Garc{\'i}a-Gavil{\'a}n, {Jes{\'u}s F.} and Nancy Babio and Estefan{\'i}a Toledo and Zhila Semnani-Azad and Cristina Razquin and Courtney Dennis and Amy Deik and Dolores Corella and Ram{\'o}n Estruch and Emilio Ros and Montserrat Fit{\'o} and Fernando Ar{\'o}s and Miquel Fiol and Jos{\'e} Lapetra and Rosa Lamuela-Raventos and Clary Clish and Miguel Ruiz-Canela and Mart{\'i}nez-Gonz{\'a}lez, {Miguel {\'A}ngel} and Frank Hu and Jordi Salas-Salvad{\'o} and Marta Guasch-Ferr{\'e}",
note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",
year = "2023",
doi = "10.1186/s12933-023-02066-1",
language = "English",
volume = "22",
journal = "Cardiovascular Diabetology",
issn = "1475-2840",
publisher = "BioMed Central Ltd.",
number = "1",

}

RIS

TY - JOUR

T1 - Olive oil consumption, plasma metabolites, and risk of type 2 diabetes and cardiovascular disease

AU - García-Gavilán, Jesús F.

AU - Babio, Nancy

AU - Toledo, Estefanía

AU - Semnani-Azad, Zhila

AU - Razquin, Cristina

AU - Dennis, Courtney

AU - Deik, Amy

AU - Corella, Dolores

AU - Estruch, Ramón

AU - Ros, Emilio

AU - Fitó, Montserrat

AU - Arós, Fernando

AU - Fiol, Miquel

AU - Lapetra, José

AU - Lamuela-Raventos, Rosa

AU - Clish, Clary

AU - Ruiz-Canela, Miguel

AU - Martínez-González, Miguel Ángel

AU - Hu, Frank

AU - Salas-Salvadó, Jordi

AU - Guasch-Ferré, Marta

N1 - Publisher Copyright: © 2023, The Author(s).

PY - 2023

Y1 - 2023

N2 - Background: Olive oil consumption has been inversely associated with the risk of type 2 diabetes (T2D) and cardiovascular disease (CVD). However, the impact of olive oil consumption on plasma metabolites remains poorly understood. This study aims to identify plasma metabolites related to total and specific types of olive oil consumption, and to assess the prospective associations of the identified multi-metabolite profiles with the risk of T2D and CVD. Methods: The discovery population included 1837 participants at high cardiovascular risk from the PREvención con DIeta MEDiterránea (PREDIMED) trial with available metabolomics data at baseline. Olive oil consumption was determined through food-frequency questionnaires (FFQ) and adjusted for total energy. A total of 1522 participants also had available metabolomics data at year 1 and were used as the internal validation sample. Plasma metabolomics analyses were performed using LC–MS. Cross-sectional associations between 385 known candidate metabolites and olive oil consumption were assessed using elastic net regression analysis. A 10-cross-validation (CV) procedure was used, and Pearson correlation coefficients were assessed between metabolite-weighted models and FFQ-derived olive oil consumption in each pair of training–validation data sets within the discovery sample. We further estimated the prospective associations of the identified plasma multi-metabolite profile with incident T2D and CVD using multivariable Cox regression models. Results: We identified a metabolomic signature for the consumption of total olive oil (with 74 metabolites), VOO (with 78 metabolites), and COO (with 17 metabolites), including several lipids, acylcarnitines, and amino acids. 10-CV Pearson correlation coefficients between total olive oil consumption derived from FFQs and the multi-metabolite profile were 0.40 (95% CI 0.37, 0.44) and 0.27 (95% CI 0.22, 0.31) for the discovery and validation sample, respectively. We identified several overlapping and distinct metabolites according to the type of olive oil consumed. The baseline metabolite profiles of total and extra virgin olive oil were inversely associated with CVD incidence (HR per 1SD: 0.79; 95% CI 0.67, 0.92 for total olive oil and 0.70; 0.59, 0.83 for extra virgin olive oil) after adjustment for confounders. However, no significant associations were observed between these metabolite profiles and T2D incidence. Conclusions: This study reveals a panel of plasma metabolites linked to the consumption of total and specific types of olive oil. The metabolite profiles of total olive oil consumption and extra virgin olive oil were associated with a decreased risk of incident CVD in a high cardiovascular-risk Mediterranean population, though no associations were observed with T2D incidence. Trial registration : The PREDIMED trial was registered at ISRCTN (http://www.isrctn.com/ , ISRCTN35739639).

AB - Background: Olive oil consumption has been inversely associated with the risk of type 2 diabetes (T2D) and cardiovascular disease (CVD). However, the impact of olive oil consumption on plasma metabolites remains poorly understood. This study aims to identify plasma metabolites related to total and specific types of olive oil consumption, and to assess the prospective associations of the identified multi-metabolite profiles with the risk of T2D and CVD. Methods: The discovery population included 1837 participants at high cardiovascular risk from the PREvención con DIeta MEDiterránea (PREDIMED) trial with available metabolomics data at baseline. Olive oil consumption was determined through food-frequency questionnaires (FFQ) and adjusted for total energy. A total of 1522 participants also had available metabolomics data at year 1 and were used as the internal validation sample. Plasma metabolomics analyses were performed using LC–MS. Cross-sectional associations between 385 known candidate metabolites and olive oil consumption were assessed using elastic net regression analysis. A 10-cross-validation (CV) procedure was used, and Pearson correlation coefficients were assessed between metabolite-weighted models and FFQ-derived olive oil consumption in each pair of training–validation data sets within the discovery sample. We further estimated the prospective associations of the identified plasma multi-metabolite profile with incident T2D and CVD using multivariable Cox regression models. Results: We identified a metabolomic signature for the consumption of total olive oil (with 74 metabolites), VOO (with 78 metabolites), and COO (with 17 metabolites), including several lipids, acylcarnitines, and amino acids. 10-CV Pearson correlation coefficients between total olive oil consumption derived from FFQs and the multi-metabolite profile were 0.40 (95% CI 0.37, 0.44) and 0.27 (95% CI 0.22, 0.31) for the discovery and validation sample, respectively. We identified several overlapping and distinct metabolites according to the type of olive oil consumed. The baseline metabolite profiles of total and extra virgin olive oil were inversely associated with CVD incidence (HR per 1SD: 0.79; 95% CI 0.67, 0.92 for total olive oil and 0.70; 0.59, 0.83 for extra virgin olive oil) after adjustment for confounders. However, no significant associations were observed between these metabolite profiles and T2D incidence. Conclusions: This study reveals a panel of plasma metabolites linked to the consumption of total and specific types of olive oil. The metabolite profiles of total olive oil consumption and extra virgin olive oil were associated with a decreased risk of incident CVD in a high cardiovascular-risk Mediterranean population, though no associations were observed with T2D incidence. Trial registration : The PREDIMED trial was registered at ISRCTN (http://www.isrctn.com/ , ISRCTN35739639).

KW - Cardiovascular disease

KW - Metabolomics

KW - Olive oil

KW - Type 2 diabetes

U2 - 10.1186/s12933-023-02066-1

DO - 10.1186/s12933-023-02066-1

M3 - Journal article

C2 - 38093289

AN - SCOPUS:85179737507

VL - 22

JO - Cardiovascular Diabetology

JF - Cardiovascular Diabetology

SN - 1475-2840

IS - 1

M1 - 340

ER -

ID: 378743987