4.7 Article

Aortic Regurgitation Is Associated With Ascending Aortic Remodeling in the Nondilated Aorta

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/ATVBAHA.120.315739

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aortic stenosis; aortic valve disease; apoptosis; extracellular matrix; fibrillin

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  1. Saarland University Medical Center

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Patients with aortic regurgitation have more severe medial degeneration in the ascending aortic wall compared to those with aortic stenosis or normal valves. This pathological remodeling includes mucoid extracellular matrix accumulation, elastin loss, elastin fragmentation, decreased expression of fibrillin and collagen. Additionally, decreased eNOS expression and increased subendothelial apoptosis were observed in the aortas with aortic regurgitation.
Objective: The probability of aortic complications in patients with bicuspid aortic valve is higher in association with aortic regurgitation (AR) compared with aortic stenosis (AS) or normally functioning valves. The objective of this study was to determine whether this is related to the specific characteristics of aneurysmatic dilatation that includes AR or whether AR itself has a negative impact on the aortic wall, independent of aneurysmatic dilatation. Approach and Results: Nondilated aortic specimens were harvested intraoperatively from individuals with tricuspid aortic valves and either AS (n=10) or AR (n=16). For controls, nondilated aortas were harvested during autopsies from individuals with tricuspid aortic valves and no evidence of aortic valve disease (n=10). Histological and immunohistochemical analyses revealed that compared with control aortas, overall medial degeneration was more severe in AR-aortas (P=0.005) but not AS-aortas (P=0.23). This pathological remodeling included mucoid extracellular matrix accumulation (P=0.005), elastin loss (P=0.003), elastin fragmentation (P=0.008), and decreased expression of fibrillin (P=0.003) and collagen (P=0.008). Furthermore, eNOS (endothelial nitric oxide synthase) expression was decreased in the intima (P=0.0008) and in vasa vasorum (P=0.004) of AR-aortas but not AS-aortas (all P>0.05). Likewise, subendothelial apoptosis was increased in AR-aortas (P=0.03) but not AS-aortas (P=0.50). Conclusions: AR has a negative effect on the nondilated ascending aortic wall. Accordingly, our results support the need for more detailed studies of the aortic wall in relation to aortic valve disease and may ultimately lead to more aggressive clinical monitoring and/or surgical criteria for patients with relevant AR.

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