TY - JOUR
T1 - A microbiota pattern associated with cardiovascular events in secondary prevention
T2 - The CORDIOPREV study
AU - Arenas-Montes, Javier
AU - Alcala-Diaz, Juan F.
AU - Garcia-Fernandez, Helena
AU - Gutierrez-Mariscal, Francisco M.
AU - Lopez-Moreno, Alejandro
AU - Luque-Cordoba, Diego
AU - Arenas-De Larriva, Antonio P.
AU - Torres-Peña, Jose D.
AU - Luque, Raul M.
AU - Prodam, Flavia
AU - Priego-Capote, Feliciano
AU - Delgado-Lista, Javier
AU - Lopez-Miranda, Jose
AU - Camargo, Antonio
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved.
PY - 2025/6/7
Y1 - 2025/6/7
N2 - Background and Aims Preventing new cardiovascular events in patients with established cardiovascular disease (CVD) is a daunting task for clinicians. Intestinal microbiota may help identify patients at risk, thus improving the strategies of secondary prevention. The aim of this study was to evaluate the baseline differences between the gut microbiota from coronary heart disease (CHD) patients suffering new major adverse cardiovascular events (MACEs) in the following 7 years, compared with CHD patients who did not undergo new MACE in this period, and to build a score associated with the risk of suffering new MACE. Methods Within the framework of the CORDIOPREV study, a clinical trial that involved 1002 patients with CHD, intestinal microbiota was examined in patients with available faecal samples (n = 679, 132 MACE), through 16S metagenomics on the Illumina MiSeq and Quiime2 software. Lipopolysaccharide (LPS) was measured using limulus amoebocyte lysate test. Results Random survival forest identified 10 bacterial taxa with a higher predictive power for MACE incidence. Receiver operating characteristic curves yielded an area under the curve of 65.2% (59.1%-71.3%) in the training set and 68.6% (59.3%-77.9%) in the validation set. The intestinal microbiota risk score was associated with a MACE incidence hazard ratio of 2.01 (95% confidence interval 1.37-3.22). Lipopolysaccharide analysis showed a greater LPS post-prandial fold change in the MACE group (P =. 005). Conclusions These results reinforce the relationship between intestinal microbiota and CVD and suggest that a microbiota profile is associated with MACE in CHD patients, in addition to higher endotoxaemia.
AB - Background and Aims Preventing new cardiovascular events in patients with established cardiovascular disease (CVD) is a daunting task for clinicians. Intestinal microbiota may help identify patients at risk, thus improving the strategies of secondary prevention. The aim of this study was to evaluate the baseline differences between the gut microbiota from coronary heart disease (CHD) patients suffering new major adverse cardiovascular events (MACEs) in the following 7 years, compared with CHD patients who did not undergo new MACE in this period, and to build a score associated with the risk of suffering new MACE. Methods Within the framework of the CORDIOPREV study, a clinical trial that involved 1002 patients with CHD, intestinal microbiota was examined in patients with available faecal samples (n = 679, 132 MACE), through 16S metagenomics on the Illumina MiSeq and Quiime2 software. Lipopolysaccharide (LPS) was measured using limulus amoebocyte lysate test. Results Random survival forest identified 10 bacterial taxa with a higher predictive power for MACE incidence. Receiver operating characteristic curves yielded an area under the curve of 65.2% (59.1%-71.3%) in the training set and 68.6% (59.3%-77.9%) in the validation set. The intestinal microbiota risk score was associated with a MACE incidence hazard ratio of 2.01 (95% confidence interval 1.37-3.22). Lipopolysaccharide analysis showed a greater LPS post-prandial fold change in the MACE group (P =. 005). Conclusions These results reinforce the relationship between intestinal microbiota and CVD and suggest that a microbiota profile is associated with MACE in CHD patients, in addition to higher endotoxaemia.
KW - CORDIOPREV
KW - Cardiovascular diseases
KW - Disease prediction
KW - Dysbiosis
KW - Intestinal microbiota
UR - https://www.scopus.com/pages/publications/105008088697
U2 - 10.1093/eurheartj/ehaf181
DO - 10.1093/eurheartj/ehaf181
M3 - Article
SN - 0195-668X
VL - 46
SP - 2104
EP - 2115
JO - European Heart Journal
JF - European Heart Journal
IS - 22
ER -