Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial

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Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial. / Wang, Dong D.; Zheng, Yan; Toledo, Estefanía; Razquin, Cristina; Ruiz-Canela, Miguel; Guasch-Ferré, Marta; Yu, Edward; Corella, Dolores; Gómez-Gracia, Enrique; Fiol, Miquel; Estruch, Ramón; Ros, Emilio; Lapetra, José; Fito, Montserrat; Aros, Fernando; Serra-Majem, Lluis; Clish, Clary B.; Salas-Salvadó, Jordi; Liang, Liming; Martínez-González, Miguel A.; Hu, Frank B.

In: International Journal of Epidemiology, Vol. 47, No. 6, 2018, p. 1830-1845.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Wang, DD, Zheng, Y, Toledo, E, Razquin, C, Ruiz-Canela, M, Guasch-Ferré, M, Yu, E, Corella, D, Gómez-Gracia, E, Fiol, M, Estruch, R, Ros, E, Lapetra, J, Fito, M, Aros, F, Serra-Majem, L, Clish, CB, Salas-Salvadó, J, Liang, L, Martínez-González, MA & Hu, FB 2018, 'Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial', International Journal of Epidemiology, vol. 47, no. 6, pp. 1830-1845. https://doi.org/10.1093/ije/dyy198

APA

Wang, D. D., Zheng, Y., Toledo, E., Razquin, C., Ruiz-Canela, M., Guasch-Ferré, M., Yu, E., Corella, D., Gómez-Gracia, E., Fiol, M., Estruch, R., Ros, E., Lapetra, J., Fito, M., Aros, F., Serra-Majem, L., Clish, C. B., Salas-Salvadó, J., Liang, L., ... Hu, F. B. (2018). Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial. International Journal of Epidemiology, 47(6), 1830-1845. https://doi.org/10.1093/ije/dyy198

Vancouver

Wang DD, Zheng Y, Toledo E, Razquin C, Ruiz-Canela M, Guasch-Ferré M et al. Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial. International Journal of Epidemiology. 2018;47(6):1830-1845. https://doi.org/10.1093/ije/dyy198

Author

Wang, Dong D. ; Zheng, Yan ; Toledo, Estefanía ; Razquin, Cristina ; Ruiz-Canela, Miguel ; Guasch-Ferré, Marta ; Yu, Edward ; Corella, Dolores ; Gómez-Gracia, Enrique ; Fiol, Miquel ; Estruch, Ramón ; Ros, Emilio ; Lapetra, José ; Fito, Montserrat ; Aros, Fernando ; Serra-Majem, Lluis ; Clish, Clary B. ; Salas-Salvadó, Jordi ; Liang, Liming ; Martínez-González, Miguel A. ; Hu, Frank B. / Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial. In: International Journal of Epidemiology. 2018 ; Vol. 47, No. 6. pp. 1830-1845.

Bibtex

@article{d46e4a0f07d44a55a3abbb9885116edf,
title = "Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial",
abstract = "Background: Perturbed lipid metabolic pathways may play important roles in the development of cardiovascular disease (CVD). However, existing epidemiological studies have focused more on discovering individual lipid metabolites for CVD risk prediction rather than assessing metabolic pathways. Methods: This study included a subcohort of 787 participants and all 230 incident CVD cases from the PREDIMED trial. Applying a network-based analytical method, we identified lipid subnetworks and clusters from a global network of 200 lipid metabolites and linked these subnetworks/clusters to CVD risk. Results: Lipid metabolites with more double bonds clustered within one subnetwork, whereas lipid metabolites with fewer double bonds clustered within other subnetworks. We identified 10 lipid clusters that were divergently associated with CVD risk. The hazard ratios [HRs, 95% confidence interval (CI)] of CVD per a 1-standard deviation (SD) increment in cluster score were 1.39 (1.17–1.66) for the hydroxylated phosphatidylcholine (HPC) cluster and 1.24 (1.11–1.37) for a cluster that included diglycerides and a monoglyceride with stearic acyl chain. Every 1-SD increase in the score of cluster that included highly unsaturated phospholipids and cholesterol esters was associated with an HR for CVD of 0.81 (95% CI, 0.67–0.98). Despite a suggestion that MedDiet modified the association between a subnetwork that included most lipids with a high degree of unsaturation and CVD, changes in lipid subnetworks/clusters during the first-year follow-up were not significantly different between intervention groups. Conclusions: The degree of unsaturation was a major determinant of the architecture of lipid metabolic network. Lipid clusters that strongly predicted CVD risk, such as the HPC cluster, warrant further functional investigations.",
keywords = "Cardiovascular disease, Lipid network, Mediterranean diet",
author = "Wang, {Dong D.} and Yan Zheng and Estefan{\'i}a Toledo and Cristina Razquin and Miguel Ruiz-Canela and Marta Guasch-Ferr{\'e} and Edward Yu and Dolores Corella and Enrique G{\'o}mez-Gracia and Miquel Fiol and Ram{\'o}n Estruch and Emilio Ros and Jos{\'e} Lapetra and Montserrat Fito and Fernando Aros and Lluis Serra-Majem and Clish, {Clary B.} and Jordi Salas-Salvad{\'o} and Liming Liang and Mart{\'i}nez-Gonz{\'a}lez, {Miguel A.} and Hu, {Frank B.}",
note = "Publisher Copyright: {\textcopyright} The Author(s) 2018.",
year = "2018",
doi = "10.1093/ije/dyy198",
language = "English",
volume = "47",
pages = "1830--1845",
journal = "International Journal of Epidemiology",
issn = "0300-5771",
publisher = "Oxford University Press",
number = "6",

}

RIS

TY - JOUR

T1 - Lipid metabolic networks, Mediterranean diet and cardiovascular disease in the PREDIMED trial

AU - Wang, Dong D.

AU - Zheng, Yan

AU - Toledo, Estefanía

AU - Razquin, Cristina

AU - Ruiz-Canela, Miguel

AU - Guasch-Ferré, Marta

AU - Yu, Edward

AU - Corella, Dolores

AU - Gómez-Gracia, Enrique

AU - Fiol, Miquel

AU - Estruch, Ramón

AU - Ros, Emilio

AU - Lapetra, José

AU - Fito, Montserrat

AU - Aros, Fernando

AU - Serra-Majem, Lluis

AU - Clish, Clary B.

AU - Salas-Salvadó, Jordi

AU - Liang, Liming

AU - Martínez-González, Miguel A.

AU - Hu, Frank B.

N1 - Publisher Copyright: © The Author(s) 2018.

PY - 2018

Y1 - 2018

N2 - Background: Perturbed lipid metabolic pathways may play important roles in the development of cardiovascular disease (CVD). However, existing epidemiological studies have focused more on discovering individual lipid metabolites for CVD risk prediction rather than assessing metabolic pathways. Methods: This study included a subcohort of 787 participants and all 230 incident CVD cases from the PREDIMED trial. Applying a network-based analytical method, we identified lipid subnetworks and clusters from a global network of 200 lipid metabolites and linked these subnetworks/clusters to CVD risk. Results: Lipid metabolites with more double bonds clustered within one subnetwork, whereas lipid metabolites with fewer double bonds clustered within other subnetworks. We identified 10 lipid clusters that were divergently associated with CVD risk. The hazard ratios [HRs, 95% confidence interval (CI)] of CVD per a 1-standard deviation (SD) increment in cluster score were 1.39 (1.17–1.66) for the hydroxylated phosphatidylcholine (HPC) cluster and 1.24 (1.11–1.37) for a cluster that included diglycerides and a monoglyceride with stearic acyl chain. Every 1-SD increase in the score of cluster that included highly unsaturated phospholipids and cholesterol esters was associated with an HR for CVD of 0.81 (95% CI, 0.67–0.98). Despite a suggestion that MedDiet modified the association between a subnetwork that included most lipids with a high degree of unsaturation and CVD, changes in lipid subnetworks/clusters during the first-year follow-up were not significantly different between intervention groups. Conclusions: The degree of unsaturation was a major determinant of the architecture of lipid metabolic network. Lipid clusters that strongly predicted CVD risk, such as the HPC cluster, warrant further functional investigations.

AB - Background: Perturbed lipid metabolic pathways may play important roles in the development of cardiovascular disease (CVD). However, existing epidemiological studies have focused more on discovering individual lipid metabolites for CVD risk prediction rather than assessing metabolic pathways. Methods: This study included a subcohort of 787 participants and all 230 incident CVD cases from the PREDIMED trial. Applying a network-based analytical method, we identified lipid subnetworks and clusters from a global network of 200 lipid metabolites and linked these subnetworks/clusters to CVD risk. Results: Lipid metabolites with more double bonds clustered within one subnetwork, whereas lipid metabolites with fewer double bonds clustered within other subnetworks. We identified 10 lipid clusters that were divergently associated with CVD risk. The hazard ratios [HRs, 95% confidence interval (CI)] of CVD per a 1-standard deviation (SD) increment in cluster score were 1.39 (1.17–1.66) for the hydroxylated phosphatidylcholine (HPC) cluster and 1.24 (1.11–1.37) for a cluster that included diglycerides and a monoglyceride with stearic acyl chain. Every 1-SD increase in the score of cluster that included highly unsaturated phospholipids and cholesterol esters was associated with an HR for CVD of 0.81 (95% CI, 0.67–0.98). Despite a suggestion that MedDiet modified the association between a subnetwork that included most lipids with a high degree of unsaturation and CVD, changes in lipid subnetworks/clusters during the first-year follow-up were not significantly different between intervention groups. Conclusions: The degree of unsaturation was a major determinant of the architecture of lipid metabolic network. Lipid clusters that strongly predicted CVD risk, such as the HPC cluster, warrant further functional investigations.

KW - Cardiovascular disease

KW - Lipid network

KW - Mediterranean diet

U2 - 10.1093/ije/dyy198

DO - 10.1093/ije/dyy198

M3 - Journal article

C2 - 30428039

AN - SCOPUS:85058610256

VL - 47

SP - 1830

EP - 1845

JO - International Journal of Epidemiology

JF - International Journal of Epidemiology

SN - 0300-5771

IS - 6

ER -

ID: 358089467