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Bile Acids and Risk of Adverse Cardiovascular Events and All-Cause Mortality in Patients with Acute Coronary Syndrome
Javier Mateu-Fabregat1,2,3, Hamza Mostafa1,2,3, Raul Sanchez-Gimenez2,4,5
1Nutrition and Metabolic Health Research Group, Department of Biochemistry and Biotechnology, Rovira i Virgili University (URV), 43201 Reus, Spain.
Insights
Bile acids (BAs) are linked to major adverse cardiovascular events (MACE) in acute coronary syndrome (ACS) patients. This study identified specific BAs and a BA score predicting MACE risk over 10 years.
Area of Science:
- Cardiovascular Medicine
- Metabolomics
- Biochemistry
Background:
- Bile acids (BAs) roles in cardiovascular health are understudied.
- Acute coronary syndrome (ACS) patients face risks of major adverse cardiovascular events (MACE).
Purpose of the Study:
- To investigate the association between plasma BAs and MACE risk in ACS patients.
- To explore the link between BAs and all-cause mortality post-ACS.
Main Methods:
- Prospective study of 309 ACS patients followed for 10 years.
- Plasma BAs quantified using liquid chromatography-tandem mass spectrometry.
- Cox regression with elastic net penalties used to identify risk-associated BAs and develop a BA score.
Main Results:
- A panel of 10 BAs was significantly associated with increased MACE risk.
- Each SD increase in the BA score correlated with a 1.35-fold higher MACE risk (HR 1.35; 95% CI 1.12-1.63).
- Four BAs were linked to all-cause mortality, but the composite score was not independently associated.
Conclusions:
- Primary and secondary bile acids may significantly contribute to MACE development in ACS.
- Bile acid profiling could offer novel strategies for managing ACS and preventing adverse cardiovascular outcomes.
Abstract:
The relationship between bile acids (BAs) and adverse cardiovascular events following acute coronary syndrome (ACS) have been little investigated. We aimed to examine the associations of BAs with the risk of cardiovascular events and all-cause mortality in ACS. We conducted a prospective study on 309 ACS patients who were followed for 10 years. Plasma BAs were quantified by liquid chromatography coupled to tandem mass spectrometry. Cox regression analyses with elastic net penalties were performed to associate BAs with MACE and all-cause mortality. Weighted scores were computed using the 100 iterated coefficients corresponding to each selected BA, and the associations of these scores with these adverse outcomes were assessed using multivariable Cox regression models. A panel of 10 BAs was significantly associated with the increased risk of MACE. The hazard ratio of MACE per SD increase in the estimated BA score was 1.35 (95% CI 1.12-1.63). Furthermore, four BAs were selected from the elastic net model for all-cause mortality, although their weighted score was not independently associated with mortality. Our findings indicate that primary and secondary BAs may play a significant role in the development of MACE. This insight holds potential for developing strategies to manage ACS and prevent adverse outcomes.
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