Abstract

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 performed 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 p=0.002; medionecrosis p=0.004; cystic necrosis p=0.07; apoptosis p<0.0001; MMP-9 amount p=0.004). 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). CONCLUSIONS: 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).
Lingua originaleEnglish
Numero di pagine1
Stato di pubblicazionePublished - 2014

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Phenotype
Aneurysm
Glycogen Synthase
Extracellular Matrix
Aorta
Dissection
Rupture
Aortic Aneurysm
Nitric Oxide Synthase Type III
Matrix Metalloproteinase 9
Peptidyl-Dipeptidase A
Matrix Metalloproteinases
Gene Frequency
Single Nucleotide Polymorphism
Fibrosis
Necrosis
Thorax
Genotype
Demography
Pharmacology

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Pisano, C; Mulla, Z; Vacirca, S (2014). CAN THE AORTIC WALL COMMUNICATE WITH US?

CAN THE AORTIC WALL COMMUNICATE WITH US? / Pisano, C; Mulla, Z; Vacirca, S.

1 pag. 2014, .

Risultato della ricerca: Other contribution

Pisano, C; Mulla, Z; Vacirca, S 2014, CAN THE AORTIC WALL COMMUNICATE WITH US?..
Pisano, C; Mulla, Z; Vacirca, S. CAN THE AORTIC WALL COMMUNICATE WITH US? 2014. 1 pag.
Pisano, C; Mulla, Z; Vacirca, S. / CAN THE AORTIC WALL COMMUNICATE WITH US?. 2014. 1 pag.
@misc{6e705995d96d4f5488ab5abc870c2bf8,
title = "CAN THE AORTIC WALL COMMUNICATE WITH US?",
abstract = "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 performed 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 p=0.002; medionecrosis p=0.004; cystic necrosis p=0.07; apoptosis p<0.0001; MMP-9 amount p=0.004). 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). CONCLUSIONS: 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).",
author = "{Pisano, C; Mulla, Z; Vacirca, S} and Giuseppina Candore and Emiliano Maresi and Giovanni Ruvolo and Balistreri, {Carmela Rita}",
year = "2014",
language = "English",
type = "Other",

}

TY - GEN

T1 - CAN THE AORTIC WALL COMMUNICATE WITH US?

AU - Pisano, C; Mulla, Z; Vacirca, S

AU - Candore, Giuseppina

AU - Maresi, Emiliano

AU - Ruvolo, Giovanni

AU - Balistreri, Carmela Rita

PY - 2014

Y1 - 2014

N2 - 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 performed 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 p=0.002; medionecrosis p=0.004; cystic necrosis p=0.07; apoptosis p<0.0001; MMP-9 amount p=0.004). 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). CONCLUSIONS: 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).

AB - 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 performed 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 p=0.002; medionecrosis p=0.004; cystic necrosis p=0.07; apoptosis p<0.0001; MMP-9 amount p=0.004). 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). CONCLUSIONS: 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).

UR - http://hdl.handle.net/10447/90125

M3 - Other contribution

ER -