# Microbiomics and metabolomics explored the characteristics of gut microbiota and metabolites in patients with aortic dissection

**Authors:** Wenkun Liu, Qiu Lin, Huiying Zhong, Jing Liang, Binmei Liu, Yunnan Hu

PMC · DOI: 10.3389/fcimb.2025.1677726 · Frontiers in Cellular and Infection Microbiology · 2025-10-08

## TL;DR

This study explores how gut bacteria and metabolites differ in people with aortic dissection, a severe heart condition, compared to healthy individuals.

## Contribution

The study identifies specific gut microbiota and metabolite changes associated with aortic dissection, offering insights for potential diagnostic models.

## Key findings

- AD patients had reduced beneficial bacteria like Bifidobacterium and increased harmful bacteria like Desulfovibrio.
- 304 metabolites were found to change significantly in AD patients, mainly related to tyrosine and taurine metabolism.
- These findings suggest gut microbiota and metabolites could help predict aortic dissection.

## Abstract

Aortic dissection (AD) is a serious and frequently fatal condition with highly variable presentations, which increases the difficulty of diagnosis during the incubation period. The objective of this study was to reveal the influence of gut microbiota and metabolites on the occurrence and development of AD. In the present study, a total of 132 volunteers were recruited, but only 50 met the experimental requirements (including 25 health controls and 25 patients with AD). Patients with AD showed the high levels of systolic blood pressure (SBP) and diastolic blood pressure (DBP), accompanied with aortic dilation. High-throughput sequencing revealed a reduction in the abundance of beneficial bacteria (containing Bifidobacterium and [Eubacterium]_eligens_group) and an increase in harmful bacteria (containing Desulfovibrio and Hungatella) in patients with AD. In addition, untargeted metabolomic identified a total of 304 metabolites that were remarkably changes in AD patients, which major involved in alactose metabolism, caffeine metabolism, tyrosine metabolism, taurine and hypotaurine metabolism, ascorbate and aldarate metabolism, and butanoate metabolism. The above data elucidate that distinct gut microbiota and metabolites in AD patients, offering reliable information to building the prediction models of AD.

## Full-text entities

- **Diseases:** AD (MESH:D000784), aortic dilation (MESH:D002311)
- **Chemicals:** ascorbate (MESH:D001205), caffeine (MESH:D002110), hypotaurine (MESH:C003949), tyrosine (MESH:D014443), alactose (-), taurine (MESH:D013654)
- **Species:** Bifidobacterium (genus) [taxon 1678], Hungatella (genus) [taxon 1649459], Desulfovibrio (genus) [taxon 872], Lachnospira eligens (species) [taxon 39485], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12540387/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12540387/full.md

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Source: https://tomesphere.com/paper/PMC12540387