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Updated: Feb 16, 2026

Porcine Model of Infrarenal Abdominal Aortic Aneurysm
Published on: November 21, 2019
Fenofibrate and Telmisartan in the Management of Abdominal Aortic Aneurysm
Sophie E Rowbotham1, Smriti M Krishna2, Corey S Moran2
1The University of Queensland; School of Medicine, Herston QLD 4006, Australia; and Department of Vascular Surgery, The Royal Brisbane and Women's Hospital, Herston QLD 4029, Australia.
Objective:
This mini-review provides the rationale and updated progress for ongoing randomized controlled trials assessing fenofibrate and telmisartan efficacy to limit abdominal aortic aneurysm (AAA) growth.
Methods/Results:
There remains an urgent need to identify a drug therapy that will limit AAA growth. Data from preclinical and human studies indicate that fenofibrate and telmisartan have the potential to slow aortic destruction. Fenofibrate has been shown to reduce serum and tissue levels of the proinflammatory protein osteopontin, as well as reducing macrophage recruitment to the aortic wall, both of which are integral processes in the development and progression of AAAs. Telmisartan acts via blockade of the angiotensin II receptor, type 1, and also as a peroxisome proliferator-activated receptor gamma agonist. In turn, this inhibits the production of a range of biomarkers associated with AAA progression, including transforming growth factor-beta one, osteoprotegerin, osteopontin and matrix metalloproteinase- 9. Based on these findings, there are currently three randomized controlled trials assessing both fenofibrate and telmisartan as potential interventions to limit aneurysm growth in AAA patients.
Conclusion:
Fenofibrate and telmisartan have potential as repurposed medications to limit AAA growth, and randomized trials for further assessment in AAA patients are ongoing.
Insights
Fenofibrate and telmisartan show promise in limiting abdominal aortic aneurysm (AAA) growth. Ongoing trials are evaluating these repurposed drugs for their potential to slow AAA progression.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Vascular Biology
Background:
- Abdominal aortic aneurysm (AAA) growth requires effective drug therapies.
- Fenofibrate and telmisartan demonstrate potential in preclinical and human studies to impede aortic destruction.
- These drugs target key inflammatory and molecular pathways implicated in AAA pathogenesis.
Purpose of the Study:
- To review the rationale and progress of ongoing randomized controlled trials.
- To assess the efficacy of fenofibrate and telmisartan in limiting abdominal aortic aneurysm growth.
- To explore the potential of repurposed medications for AAA treatment.
Main Methods:
- Review of preclinical and human studies on fenofibrate and telmisartan.
- Analysis of mechanisms of action, including osteopontin reduction and inflammatory pathway modulation.
- Identification of ongoing randomized controlled trials evaluating these agents in AAA patients.
Main Results:
- Fenofibrate reduces osteopontin and macrophage recruitment in the aortic wall.
- Telmisartan blocks angiotensin II receptor type 1 and activates PPARγ, inhibiting AAA biomarkers.
- Multiple biomarkers including TGF-β1, OPG, osteopontin, and MMP-9 are affected by telmisartan.
Conclusions:
- Fenofibrate and telmisartan are potential repurposed medications for limiting AAA growth.
- Randomized trials are currently underway to further evaluate their efficacy in AAA patients.
- These agents offer a promising avenue for pharmacological intervention in AAA management.
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