Abstract
Background: Elevated serum bile acids (BA) are harmful to the heart and alterations in the BA composition have been suggested to cause cardiovascular disturbances in cirrhosis. Aim: To investigate any associations between specific groups or individual serum BA and structural and functional cardiac abnormalities in patients with cirrhosis. Methods: An explorative study in 86 patients with cirrhosis. All participants underwent extensive cardiac assessment, including cardiac MRI with quantification of myocardial extracellular volume (ECV), which is indicative of diffuse myocardial fibrosis. A panel of 15 individual serum BA and C4, a marker of de novo bile acid synthesis, were assessed. Results: Patients with advanced cirrhosis had higher levels of total BA and conjugated BA, as well as lower C4 levels (p < 0.001). Conjugated BA levels were higher in patients with a high cardiac index (p < 0.001), increased left atrial volume index (LAVI) (p < 0.001), and in those with an abnormal myocardial ECV (p < 0.05). We also found several strong correlations between conjugated BA, both as a group and individually, and parameters of cardiac dysfunction. In a model adjusted for sex, age, BMI and MELD, conjugated BA remained significantly associated with LAVI, septal e′, left ventricular volumes and cardiac index. In addition, taurocholic acid correlated closely with hepatic venous pressure gradient (HVPG) (p = 0.01). Conclusions: Increased serum concentrations of conjugated BA are associated with several cardiac parameters, indicating a potential role in the development of hyperdynamic circulation and cardiac dysfunction in cirrhosis. Moreover, taurine-conjugated BA are associated with portal hypertension.
Original language | English |
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Journal | Alimentary Pharmacology and Therapeutics |
Volume | 58 |
Issue number | 4 |
Pages (from-to) | 453-462 |
Number of pages | 10 |
ISSN | 0269-2813 |
DOIs | |
Publication status | Published - Aug 2023 |
Bibliographical note
Funding Information:The work was supported by grants from the Arvid Nilssons Foundation and the Capital Region of Denmark Foundation for Health Research.
Funding Information:
Andrei Voiosu: The contribution of AV to this work was supported in part by a grant of the Ministry of Research, Innovation and Digitization, CNCS—UEFISCDI, project number PN‐III‐P1‐1.1‐PD‐2021‐0180, within PNCDI III. None of the other authors have any conflicts of interest to be declared.
Publisher Copyright:
© 2023 John Wiley & Sons Ltd.