Degeneration mechanisms and advancements in optimization for preparation and crosslinking strategy of pericardium-based bioprosthetic heart valves.

Xueyu Huang, Bangquan Wei, Lepeng Chen, Li Yang, Cheng Zheng, Yunbing Wang
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Abstract

Valvular heart disease (VHD), clinically manifested as the malfunction of heart valves, greatly threatens public health worldwide. The morbidity and mortality of VHD increase significantly with age, and the high prevalence of VHD in aging society has prompted the urgency for effective treatment. Prosthetic heart valve replacement is currently recognized as the gold standard for VHD treatment. Bioprosthetic heart valves (BHVs), generally manufactured from glutaraldehyde crosslinked xenogeneic tissue, exhibited better hemodynamics and lower thrombogenicity than mechanical heart valves (MHVs) and could be implanted by transcatheter valve replacement systems, which markedly improved the efficiency of VHD therapy, especially for the elderly patients. However, BHVs degenerate within 10-15 years after implantation, which is greatly associated with their defects including cytotoxicity, calcification, immune response, matrix degradation, mechanical damage, and thrombosis. To prolong the service life of BHVs, recent studies have developed a series of innovative modification strategies to improve the biocompatibility, mechanical performance, matrix components stability, anticalcification, and antithrombotic properties of conventional glutaraldehyde crosslinked BHVs. Moreover, a series of new crosslinking and modification strategies have been proposed and developed to fabricate non-glutaraldehyde crosslinked BHVs with good stability, biocompatibility, hemocompatibility, anticalcification property, durability, and hydrodynamics. In this review, we first summarized the defects of BHVs and the related reasons from the perspective of biomaterials, and then comprehensively detailed the functional modification strategies for BHVs based on glutaraldehyde crosslinking. We provided detailed insights into novel non-glutaraldehyde crosslinking and modification strategies for BHVs. Finally, the current challenges and prospects of BHVs were also discussed. STATEMENT OF SIGNIFICANCE: Bioprosthetic heart valves (BHVs) currently face challenges such as cytotoxicity, thrombosis, calcification, and immunoinflammatory responses, which contribute to structural valve degeneration and reduce the longevity of BHVs. This review provides a comprehensive introduction to the detailed defects associated with glutaraldehyde crosslinked BHVs from the perspective of biomaterials. It then thoroughly elaborates on the modification strategies based on glutaraldehyde crosslinking, as well as detailed insights into novel non-glutaraldehyde crosslinking strategies for BHVs. Finally, the challenges and prospects facing BHVs are discussed.

心包基生物人工心脏瓣膜退行性变机制及制备及交联策略优化研究进展。
瓣膜性心脏病(VHD)在临床上表现为心脏瓣膜功能障碍,严重威胁着全球公众的健康。VHD的发病率和死亡率随着年龄的增长而显著增加,老龄化社会中VHD的高患病率促使了有效治疗的紧迫性。人工心脏瓣膜置换术是目前公认的VHD治疗的金标准。生物人工心脏瓣膜(bhv)通常由戊二醛交联异种组织制造,比机械心脏瓣膜(mhv)具有更好的血流动力学和更低的血栓形成性,可以通过经导管瓣膜置换系统植入,显着提高VHD治疗的效率,特别是对于老年患者。然而,bhv在植入后10-15年内发生退化,这与bhv的细胞毒性、钙化、免疫反应、基质降解、机械损伤和血栓形成等缺陷密切相关。为了延长bhv的使用寿命,最近的研究开发了一系列创新的改性策略,以提高传统戊二醛交联bhv的生物相容性、机械性能、基质组分稳定性、抗钙化和抗血栓性。此外,还提出并开发了一系列新的交联和改性策略,以制备具有良好稳定性、生物相容性、血液相容性、抗钙化性能、耐久性和流体动力学性能的非戊二醛交联bhv。本文首先从生物材料的角度综述了bhv的缺陷及其原因,然后全面阐述了基于戊二醛交联的bhv功能修饰策略。我们提供了新的非戊二醛交联和bhv修饰策略的详细见解。最后,讨论了bhv目前面临的挑战和前景。意义声明:生物人工心脏瓣膜(bhv)目前面临着细胞毒性、血栓形成、钙化和免疫炎症反应等挑战,这些问题会导致瓣膜结构变性,降低bhv的使用寿命。本文从生物材料的角度全面介绍了戊二醛交联bhv相关的缺陷。然后详细阐述了基于戊二醛交联的改性策略,以及对bhv的新型非戊二醛交联策略的详细见解。最后,讨论了bhv面临的挑战和前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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