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Updated: Nov 16, 2025

Ultrasound Imaging of the Thoracic and Abdominal Aorta in Mice to Determine Aneurysm Dimensions
Published on: March 8, 2019
Is there an immunogenomic difference between thoracic and abdominal aortic aneurysms?
Zhi Jiun Yap1, Monira Sharif2, Mohamad Bashir3
1Department of Anaesthetic, Dorset County Hospital, Dorset, England.
Abdominal aortic aneurysms (AAA) expand faster than thoracic aortic aneurysms (TAA). Genetic testing may help identify individuals at risk for both AAA and TAA in the future.
Area of Science:
- Cardiovascular Research
- Genetics and Immunology
Background:
- Aortic aneurysms, particularly abdominal aortic aneurysms (AAA) and thoracic aortic aneurysms (TAA), pose significant health risks due to potential dissection or rupture.
- AAA is more prevalent than TAA, with TAA often underdiagnosed due to lack of screening.
- Understanding the natural history, genetic factors, and immunological differences is crucial for effective management and improved survival rates.
Purpose of the Study:
- To conduct a comprehensive literature review on the natural history, immunology, and genetic distinctions between AAAs and TAAs.
- To compare the expansion rates and pathogenetic mechanisms of AAAs and TAAs.
Main Methods:
- Systematic literature search conducted across OVID, SCOPUS, and PubMed databases.
- Review and synthesis of existing research on aortic aneurysm natural history, genetics, and immunology.
Main Results:
- Abdominal aortic aneurysms (AAA) exhibit a faster expansion rate (0.3-0.45 cm/year) compared to thoracic aortic aneurysms (TAA) (up to 0.3 cm/year).
- Degradation of the aortic extracellular matrix by Matrix metalloproteinases (MMPs) is a key factor in AAA pathogenesis.
- Overactive Transforming growth factor-beta (TGF-β) signaling is a major contributor to TAA pathogenesis.
Conclusions:
- Differences in pathogenetic mechanisms, including MMPs in AAA and TGF-β in TAA, highlight distinct biological pathways.
- Future genetic testing holds promise for identifying individuals predisposed to developing either AAA or TAA, enabling earlier detection and intervention.
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