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Glycation and Serum Albumin Infiltration Contribute to the Structural Degeneration of Bioprosthetic Heart Valves

Valvular heart diseases are associated with significant cardiovascular morbidity and mortality, and often require surgical and/or percutaneous repair or replacement. Valve replacement is limited to mechanical and biological prostheses, the latter of which circumvent the need for lifelong anticoagula...

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Detalles Bibliográficos
Autores principales: Frasca, Antonio, Xue, Yingfei, Kossar, Alexander P., Keeney, Samuel, Rock, Christopher, Zakharchenko, Andrey, Streeter, Matthew, Gorman, Robert C., Grau, Juan B., George, Isaac, Bavaria, Joseph E., Krieger, Abba, Spiegel, David A., Levy, Robert J., Ferrari, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452200/
https://www.ncbi.nlm.nih.gov/pubmed/32875167
http://dx.doi.org/10.1016/j.jacbts.2020.06.008
Descripción
Sumario:Valvular heart diseases are associated with significant cardiovascular morbidity and mortality, and often require surgical and/or percutaneous repair or replacement. Valve replacement is limited to mechanical and biological prostheses, the latter of which circumvent the need for lifelong anticoagulation but are subject to structural valve degeneration (SVD) and failure. Although calcification is heavily studied, noncalcific SVD, which represent roughly 30% of BHV failures, is relatively underinvestigated. This original work establishes 2 novel and interacting mechanisms—glycation and serum albumin incorporation—that occur in clinical valves and are sufficient to induce hallmarks of structural degeneration as well as functional deterioration.