Literature DB >> 22194275

Histological and genetic studies in patients with bicuspid aortic valve and ascending aorta complications.

Calogera Pisano1, Emiliano Maresi, Carmela Rita Balistreri, Giuseppina Candore, Daniele Merlo, Khalil Fattouch, Giuseppe Bianco, Giovanni Ruvolo.   

Abstract

OBJECTIVES: Aneurysm diameter and growing rate does not represent a definite parameter for operation in bicuspid aortic valve (BAV), ascending aortic aneurysm and normal root patients. Thus, we investigated histological and immunohistochemical aspects of different segments of ascending aorta (precisely, aortic root without dilatation, aneurysmatic tubular portion, dissected ascending aorta) and genetic features of patients with BAV and ascending aorta complication (aneurysm or dissection).
METHODS: Aorta tissue samples of 24 BAV patients were examined. The patients comprised of 18 men and 6 women; the mean age was 54.2 ± 14.3 years. All patients underwent composite aortic root replacement (button Bentall operation). Multiple histological sections were prepared from each aortic specimen. The evaluated features included elastic fibre fragmentation, cystic medial change, smooth muscle cell necrosis, medial fibrosis, and the markers of medial apoptosis and the metalloproteinases. Furthermore, genetic risk factors were also investigated.
RESULTS: The same medial degenerative lesions in tissue samples of different aorta segments (precisely of aortic root without dilatation, and aneurysmatic ascending aorta portion) were observed. More significant associations between single nucleotide polymorphisms (-786T/C endothelial nitric oxide synthase enzyme, D/I angiotensin-converting enzyme, -1562C/T metalloproteinase-9 and -735C/T metalloproteinase-2) and aneurysm risk were detected in BAV patients than in controls.
CONCLUSIONS: Based on our histological and genetic data, we underline that a surgical approach in patients with BAV, ascending aortic aneurysm and normal root, should consider not only the diameter of the aneurysmatic aortic portion but also the histological features of the whole ascending aorta and the genetic risk profile.

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Year:  2011        PMID: 22194275      PMCID: PMC3290383          DOI: 10.1093/icvts/ivr114

Source DB:  PubMed          Journal:  Interact Cardiovasc Thorac Surg        ISSN: 1569-9285


  25 in total

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4.  Failure to prevent progressive dilation of ascending aorta by aortic valve replacement in patients with bicuspid aortic valve: comparison with tricuspid aortic valve.

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  18 in total

1.  The genetic and molecular basis of bicuspid aortic valve associated thoracic aortopathy: a link to phenotype heterogeneity.

Authors:  Ratnasari Padang; Paul G Bannon; Richmond Jeremy; David R Richmond; Christopher Semsarian; Michael Vallely; Michael Wilson; Tristan D Yan
Journal:  Ann Cardiothorac Surg       Date:  2013-01

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3.  Aortic stiffness and left ventricular diastolic function in children with well-functioning bicuspid aortic valves.

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5.  A shifting approach to management of the thoracic aorta in bicuspid aortic valve.

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6.  Subtypes of bicuspid aortic valves in coarctation of the aorta.

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7.  Elevated oxidative stress in the aortic media of patients with bicuspid aortic valve.

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8.  Gender-dependent aortic remodelling in patients with bicuspid aortic valve-associated thoracic aortic aneurysm.

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9.  Bicuspid aortic valve disease and ascending aortic aneurysms: gaps in knowledge.

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10.  Preliminary biomarkers for identification of human ascending thoracic aortic aneurysm.

Authors:  Kendra M Black; Akihiro Masuzawa; Robert C Hagberg; Kamal R Khabbaz; Mary E Trovato; Verna M Rettagliati; Manoj K Bhasin; Simon T Dillon; Towia A Libermann; Ioannis K Toumpoulis; Sidney Levitsky; James D McCully
Journal:  J Am Heart Assoc       Date:  2013-11-14       Impact factor: 5.501

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