CRT-724 Can the Aortic Wall Communicate with Us?

Objective: Association between aortic aneurysm wall and risk of rupture or dissection. Methods: Aortic specimens were obtained from 73 patients (51 men and 22 women, whose median age 61.7` 10.7 years) undergoing surgical repair of thoracic ascending aneurysm (TAA). Histopathological and immunohistochemical analyses were per- formed using adequate tissue specimens, appropriate techniques and criteria. Furthermore, genetic risk factors were also investigated. Results: We identified three phenotypes of TAAs with different quality of aortic wall at the time of operation: phenotype I (normal wall); phenotype II (moderate wall thickness); phenotype III (thin and weak wall). No significant differences were detected in term of demographic and clinical data, co-morbidity conditions and pharmacological treatments. In contrast, significant statistical differences were observed by comparing abnormalities of extracellular matrix components among three phenotypes (fibrosis p<0.005; elastic fragmentation p1⁄40.002; medionecrosis p1⁄40.004; cystic necrosis p1⁄40.07; apoptosis p<0.0001; MMP-9 amount p1⁄40.004). In addition, significant differences both in genotype distributions and allele frequencies were observed for following SNPs (Single Nucleotide Polymorphism): -1562C/T MMP-9 (Metalloproteinases-9), -786T/C eNOs (endothelial Nitric Oxide Synthase) and D/I ACE (Angiotensin Converting Enzyme). Conclusion: Aneurysm with thin and weak wall at the time of operation should seem genetically and mainly associated with extracellular matrix disorders of aorta wall and consequently with aorta aneurysm complications (rupture and dissection).