Alpha-Amino Oleic Acid as Anticalcification Agent for Porcine Bioprosthetic Heart Valves: A Narrative Review.

IF 1.4 0 CARDIAC & CARDIOVASCULAR SYSTEMS
Lennart Vanglabeke, Marie Van den Bosch, Kenny Anseele, Tom Verbelen, Bart Meuris
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Abstract

Objective: Calcification remains the principal mechanism limiting the durability of bioprosthetic heart valves. Alpha-amino oleic acid (AOA) was developed as an anticalcification treatment to preserve tissue integrity. This review synthesizes preclinical and clinical evidence on the efficacy of AOA-treated bioprosthetic valves.

Methods: A narrative review was conducted using major biomedical databases to assess experimental and clinical studies evaluating AOA-treated tissues and valve platforms. Evidence from in vitro experiments, small/large animal models, and long-term clinical cohorts was qualitatively synthesized, with emphasis on calcification, structural valve degeneration, and durability outcomes.

Results: Preclinical studies consistently demonstrated significant reductions in leaflet calcification in AOA-treated tissues compared with glutaraldehyde-fixed controls, across multiple models. These effects were most pronounced in leaflet tissue, whereas protection of the aortic wall or conduit tissue was less consistent. Large-animal models confirmed delayed mineralization and preservation of leaflet flexibility, but revealed susceptibility of non-leaflet components to calcific degeneration. Clinically, long-term follow-up of several surgical valve platforms incorporating AOA showed acceptable freedom from structural valve degeneration extending beyond ten years in selected patient populations. Durability remains strongly age-dependent, and late valve failures can still be associated with progressive calcification. Evidence from newer valve platforms is becoming available through various long-term follow-up studies.

Conclusion: AOA provides effective anticalcification protection of bioprosthetic valve leaflets, supporting durable clinical performance in surgical platforms.

α -氨基酸油酸作为猪生物人工心脏瓣膜抗钙化剂的研究进展。
目的:钙化仍然是限制生物人工心脏瓣膜耐久性的主要机制。α -氨基酸油酸(AOA)是一种抗钙化治疗,以保持组织的完整性。本文综述了aoa治疗生物瓣膜疗效的临床前和临床证据。方法:利用主要生物医学数据库对评价aoa治疗组织和瓣膜平台的实验和临床研究进行综述。来自体外实验、小型/大型动物模型和长期临床队列的证据被定性地合成,重点是钙化、结构性瓣膜变性和耐久性结果。结果:临床前研究一致表明,在多个模型中,与戊二醛固定对照组相比,aoa处理组织的小叶钙化显著减少。这些影响在小叶组织中最为明显,而对主动脉壁或导管组织的保护则不太一致。大型动物模型证实了延迟矿化和保留小叶弹性,但显示非小叶成分对钙化变性的易感性。临床上,几个手术瓣膜平台合并AOA的长期随访显示,在选定的患者群体中,结构性瓣膜退变的自由程度可达10年以上。瓣膜的耐久性仍与年龄密切相关,晚期瓣膜失效仍可能与进行性钙化有关。通过各种长期随访研究,新的阀门平台的证据越来越多。结论:AOA为生物假体瓣膜小叶提供了有效的抗钙化保护,支持手术平台持久的临床性能。
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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