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Updated: Jul 7, 2026

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Published on: August 24, 2019
Elevated plasma MMP1 and MMP9 are associated with abdominal aortic aneurysm rupture
W R W Wilson1, M Anderton, E C Choke
1Department of Surgery, University of Leicester, United Kingdom.
Background:
The role of matrix metalloproteinases (MMPs) in abdominal aortic aneurysm (AAA) formation is well established. However the changes in plasma MMP levels with AAA rupture have not been reported. The aim of this study was to determine circulating levels of MMPs in non-ruptured and ruptured AAA immediately prior to open repair.
Methods:
Concentrations of MMPs and their endogenous tissue inhibitors (TIMPs) were quantified using ELISA in pre-operative plasma samples from non-ruptured and ruptured AAA.
Results:
MMP1 and MMP9 were elevated in the plasma of ruptured AAA versus non-ruptured AAA. A four-fold elevation in pre-operative plasma MMP9 was associated with non-survival at 30 days from rupture surgery compared with those surviving for greater than 30 days.
Conclusion:
In conclusion, these findings support the role of MMPs in AAA pathogenesis. Elevation of MMP9 was associated with ruptured aneurysm related 30-day mortality and may represent a survival indicator in this group.
Insights
Matrix metalloproteinases (MMPs) are linked to abdominal aortic aneurysm (AAA) formation. Elevated MMP9 levels in ruptured AAA patients correlate with increased 30-day mortality, suggesting it as a survival indicator.
Area of Science:
- Vascular Biology
- Biomarkers
- Aneurysm Pathogenesis
Background:
- Matrix metalloproteinases (MMPs) are implicated in abdominal aortic aneurysm (AAA) development.
- Circulating MMP levels during AAA rupture remain under-investigated.
- Understanding these changes is crucial for predicting AAA rupture outcomes.
Purpose of the Study:
- To quantify plasma levels of MMPs and their inhibitors (TIMPs) in patients with non-ruptured and ruptured AAA.
- To investigate the association between MMP levels and AAA rupture.
- To identify potential biomarkers for AAA rupture prognosis.
Main Methods:
- Pre-operative plasma samples from AAA patients were analyzed using ELISA.
- Concentrations of various MMPs and TIMPs were measured.
- Comparison of MMP and TIMP levels between ruptured and non-ruptured AAA groups.
Main Results:
- Plasma levels of MMP1 and MMP9 were significantly higher in ruptured AAA patients compared to non-ruptured AAA patients.
- A four-fold increase in pre-operative plasma MMP9 was associated with 30-day non-survival after rupture surgery.
- MMP9 elevation may indicate a poorer prognosis in ruptured AAA.
Conclusions:
- These findings reinforce the role of MMPs in the pathogenesis of AAA.
- Elevated MMP9 levels in ruptured AAA are linked to increased 30-day mortality.
- MMP9 could serve as a valuable prognostic biomarker for ruptured AAA patients.
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