Hamana Tomoyo, Sekimoto Teruo, Finn Aloke V, Virmani Renu
CVPath Institute, Inc, Gaithersburg, MD 20878, USA.
School of Medicine, University of Maryland, Baltimore, MD 21201, USA.
Rev Cardiovasc Med. 2025 Apr 17;26(4):28185. doi: 10.31083/RCM28185. eCollection 2025 Apr.
Aortic stenosis (AS) is a significant and growing concern, with a prevalence of 2-3% in individuals aged over 65 years. Moreover, with an aging global population, the prevalence is anticipated to double by 2050. Indeed, AS can arise from various etiologies, including calcific trileaflets, congenital valve abnormalities (e.g., bicuspid and unicuspid valves), and post-rheumatic, whereby each has a distinct influence that shapes the onset and progression of the disease. The normal aortic valve has a trilaminar structure comprising the fibrosa, spongiosa, and ventricularis, which work together to maintain its function. In calcific AS, the disease begins with early calcification starting in high mechanical stress areas of the valve and progresses slowly over decades, eventually leading to extensive calcification resulting in impaired valve function. This process involves mechanisms similar to atherosclerosis, including lipid deposition, chronic inflammation, and mineralization. The progression of calcific AS is strongly associated with aging, with additional risk factors including male gender, smoking, dyslipidemia, and metabolic syndrome exacerbating the condition. Conversely, congenital forms of AS, such as bicuspid and unicuspid aortic valves, result in an earlier disease onset, typically 10-20 years earlier than that observed in patients with a normal tricuspid aortic valve. Rheumatic AS, although less common in developed countries due to effective antibiotic treatments, also exhibits age-related characteristics, with an earlier onset in individuals who experienced rheumatic fever in their youth. The only curative therapies currently available are surgical and transcatheter aortic valve replacement (TAVR). However, these options are sometimes too invasive for older patients; thus, management of AS, particularly in older patients, requires a comprehensive approach that considers age, disease severity, comorbidities, frailty, and each patient's individual needs. Although the valves used in TAVR demonstrate promising midterm durability, long-term data are still required, especially when used in younger individuals, usually with low surgical risk. Moreover, understanding the causes and mechanisms of structural valve deterioration is crucial for appropriate treatment selections, including valve selection and pharmacological therapy, since this knowledge is essential for optimizing the lifelong management of AS.
主动脉瓣狭窄(AS)是一个日益严重且备受关注的问题,在65岁以上人群中的患病率为2%-3%。此外,随着全球人口老龄化,预计到2050年患病率将翻倍。事实上,AS可由多种病因引起,包括钙化三叶瓣、先天性瓣膜异常(如二叶瓣和单叶瓣)以及风湿后病变,每种病因对疾病的发生和发展都有独特的影响。正常主动脉瓣具有三层结构,由纤维层、海绵层和心室层组成,它们共同维持其功能。在钙化性AS中,疾病始于瓣膜高机械应力区域的早期钙化,并在数十年中缓慢进展,最终导致广泛钙化,从而损害瓣膜功能。这个过程涉及与动脉粥样硬化相似的机制,包括脂质沉积、慢性炎症和矿化。钙化性AS的进展与衰老密切相关,其他风险因素包括男性、吸烟、血脂异常和代谢综合征,这些因素会加剧病情。相反,先天性AS形式,如二叶式和单叶式主动脉瓣,会导致疾病更早发作,通常比正常三叶主动脉瓣患者早10-20年。风湿性AS虽然在发达国家由于有效的抗生素治疗不太常见,但也表现出与年龄相关的特征,在年轻时患过风湿热的个体中发病较早。目前唯一的治愈性疗法是外科手术和经导管主动脉瓣置换术(TAVR)。然而,这些选择对于老年患者有时侵入性过大;因此,AS的管理,尤其是老年患者,需要一种综合方法,考虑年龄、疾病严重程度、合并症、虚弱程度以及每个患者的个体需求。尽管TAVR中使用的瓣膜显示出有前景的中期耐久性,但仍需要长期数据,特别是在用于手术风险通常较低的年轻个体时。此外,了解结构性瓣膜退化的原因和机制对于适当的治疗选择至关重要,包括瓣膜选择和药物治疗,因为这些知识对于优化AS的终身管理至关重要。