# Conjugated bile acids are elevated in severe calcific aortic valve stenosis

**Authors:** Hannah Zhang, Negar Atefi, Arun Surendran, Jun Han, David R. Goodlett, Davinder S. Jassal, Ashish Shah, Amir Ravandi

PMC · DOI: 10.1016/j.jlr.2025.100830 · 2025-05-22

## TL;DR

This study finds that conjugated bile acids are higher in severe aortic valve stenosis, suggesting a link between bile acid metabolism and heart valve disease.

## Contribution

The study identifies specific elevated bile acids in severe calcific aortic valve stenosis and links them to disease severity.

## Key findings

- Five bile acids are significantly elevated in moderate and severe aortic stenosis.
- Conjugated primary and secondary bile acids are increased in stenotic valves compared to mild cases.
- Bile acid composition can distinguish valve severity using K-means clustering.

## Abstract

Calcific aortic valve (AV) stenosis (CAVS) is a disease associated with significant morbidity and mortality in the aging population. Recently, bile acids have been shown to play a significant role in many disease processes, and untargeted metabolomic analyses of CAVS patient valves have shown a disrupted bile acid pathway. We aimed to understand the changes in human valvular bile acids in relation to CAVS severity. A total of 100 human AVs were collected from patients undergoing AV replacement surgery. Bile acids were quantified by ultrahigh performance liquid chromatography coupled to MS/MS. Patients with mild aortic stenosis (AS) showed a distinct valvular bile acid composition compared with moderate and severe AS groups, with five bile acids being significantly elevated in patients with moderate and severe AS. These included norcholic, nordeoxycholic, glycodeoxycholic, glycocholic, and taurodeoxycholic acid. When classified by calcification score, five species were significantly different between mild and severe AS groups; four bile acids were similar when stratified based on AS severity. Using K-means clustering, we were able to distinguish valve severity by their bile acid composition. Grouping bile acids by conjugation and by primary versus secondary revealed that conjugated primary and secondary bile acids were significantly increased in stenotic valves compared with the mild AS group. Conjugated bile acids are significantly elevated in the valvular tissue of patients with severe calcific AS. These findings suggest a potential link between liver and gut microbiome physiology and bile acid pathways in contributing to the pathophysiology of valvular stenosis.

## Linked entities

- **Chemicals:** norcholic acid (PubChem CID 158738), nordeoxycholic acid (PubChem CID 193905), glycodeoxycholic acid (PubChem CID 3035026), glycocholic acid (PubChem CID 10140), taurodeoxycholic acid (PubChem CID 2733768)
- **Diseases:** aortic stenosis (MONDO:0042981)

## Full-text entities

- **Diseases:** AS (MESH:D001024), calcification (MESH:D002114), valvular stenosis (MESH:D011666)
- **Chemicals:** taurodeoxycholic acid (MESH:D013657), Bile acids (MESH:D001647), Conjugated bile acids (-)
- **Species:** gut metagenome (species) [taxon 749906], Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12214273/full.md

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Source: https://tomesphere.com/paper/PMC12214273