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Updated: Jul 6, 2025

Quantitative Micro-CT Analysis of Aortopathy in a Mouse Model of β-aminopropionitrile-induced Aortic Aneurysm and Dissection
Published on: July 16, 2018
Screening plasma metabolites as potential biomarkers for type B aortic dissection
Heng Xu1, Dongxiao Fan2,3, Yupeng Lin1
1Department of Cardiovascular Medicine, Jieyang People's Hospital, Jieyang, China.
This study identified three plasma metabolites linked to the risk of type B aortic dissection (TBAD) and developed a risk score model. It also found specific metabolites associated with TBAD severity in hypertensive patients.
Area of Science:
- Cardiovascular Research
- Metabolomics
- Biomarker Discovery
Background:
- Aortic dissection (AD) is a critical cardiovascular condition.
- Current imaging lacks biological insights into AD.
- Type B AD (TBAD) requires identification of predictive biomarkers.
Purpose of the Study:
- To identify plasma metabolites associated with the risk of type B aortic dissection (TBAD).
- To develop a metabolites risk score (MRS) model for TBAD risk prediction.
- To identify plasma metabolites related to the severity of TBAD.
Main Methods:
- Cross-sectional study of 16 hypertensive patients with TBAD and 7 without.
- Plasma metabolomics analysis.
- Logistic regression and LASSO regression for MRS model development and metabolite screening.
Main Results:
- Three metabolites (1,5-anhydro-D-glucitol, D-(+)-sucrose, PC(O-16:0/0:0)) were identified for TBAD risk.
- An MRS model was constructed using these metabolites.
- Hydrocinnamic acid, glycine deoxycholic acid, and glycochenodeoxycholic acid were associated with TBAD severity.
Conclusions:
- Identified key plasma metabolites for TBAD risk and severity.
- Developed a novel MRS model for TBAD risk.
- Findings offer potential TBAD biomarkers and insights into disease mechanisms.
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