AI Article Synopsis

  • Elastic fiber fragmentation (EFF) is a significant feature of aortic valve disease (AVD) and is linked to abnormal blood vessel growth (angiogenesis) associated with inflammation.
  • The study analyzed aortic valve tissue from both early-onset (<40 years) and late-onset (≥40 years) AVD patients, using various techniques to assess regional anatomy and pathology.
  • Findings indicate that early-onset AVD shows signs of angiogenesis without inflammation or atherosclerosis, suggesting a relationship between EFF and the development of new blood vessels in this condition, which could lead to new treatment options.

Article Abstract

Elastic fiber fragmentation (EFF) is a hallmark of aortic valve disease (AVD), and neovascularization has been identified as a late finding related to inflammation. We sought to characterize the relationship between early EFF and aberrant angiogenesis. To examine disease progression, regional anatomy and pathology of aortic valve tissue were assessed using histochemistry, immunohistochemistry, and electron microscopy from early-onset (<40 yo) and late-onset (≥40 yo) non-syndromic AVD specimens. To assess the effects of EFF on early AVD processes, valve tissue from Williams and Marfan syndrome patients was also analyzed. Bicuspid aortic valve was more common in early-onset AVD, and cardiovascular comorbidities were more common in late-onset AVD. Early-onset AVD specimens demonstrated angiogenesis without inflammation or atherosclerosis. A distinct pattern of elastic fiber components surrounded early-onset AVD neovessels, including increased emilin-1 and decreased fibulin-5. Different types of EFF were present in Williams syndrome (WS) and Marfan syndrome (MFS) aortic valves; WS but not MFS aortic valves demonstrated angiogenesis. Aberrant angiogenesis occurs in early-onset AVD in the absence of inflammation, implicating EFF. Elucidation of underlying mechanisms may inform the development of new pharmacologic treatments.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303641PMC
http://dx.doi.org/10.3390/jcdd8070075DOI Listing

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