老年动脉粥样硬化性心血管疾病和先进心血管成像技术的作用

Jie Jun Wong, Rilong Hong, Louis L. Y. Teo, Ru-San Tan, Angela S. Koh
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摘要

衰老和炎症是心血管疾病发病机制的关键因素。衰老的特点是慢性、全身性、失调性炎症和功能失调性免疫反应,即炎症衰老,会造成累积性心血管损伤。这些有害过程会导致上皮功能障碍、免疫浸润、泡沫细胞沉积和钙化,从而形成动脉粥样硬化斑块。随着年龄的增长,上皮细胞和血管平滑肌细胞衰老,获得与衰老相关的分泌表型,从而分泌促炎症和促纤维化因子,产生自分泌和旁分泌效应,延续组织衰老和最终衰竭的恶性循环,进一步促进动脉粥样硬化的形成。最近有证据表明,抗炎疗法可降低心血管风险;然而,脱靶不良反应的可能性可能会限制抗炎疗法的应用。此外,全身炎症标志物在定位心血管活动性炎症方面不够精确,而传统的心血管成像方法只能检测疾病晚期的结构变化。靶向分子成像通过描述心血管炎症的细胞生物学机制,提供了成像引导的精准治疗和早期上游预防方法,并有望彻底改变早期动脉粥样硬化疾病的个性化治疗。在此,我们将探讨分子成像技术在与衰老相关的动脉粥样硬化性心血管疾病机制方面的最新进展。我们强调了将分子成像转化为临床实践所面临的挑战,并提出了这些新型诊断模式的未来发展方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atherosclerotic cardiovascular disease in aging and the role of advanced cardiovascular imaging
Aging and inflammation are key drivers in the pathogenesis of cardiovascular disease. Aging is characterized by chronic, systemic, dysregulated inflammation and dysfunctional immune responses ― termed inflammaging ― that give rise to cumulative cardiovascular damage. These noxious processes promote epithelial dysfunction, immune infiltration, foam cell deposition, and calcification, which result in atherosclerotic plaque formation. With aging, epithelial and vascular smooth muscle cell senescence further contribute to atherogenesis by the acquisition of the senescence-associated secretory phenotype, consequently secreting pro-inflammatory and pro-fibrotic factors that exert autocrine and paracrine effects to perpetuate a vicious cycle of tissue aging and eventual failure. Recent evidence has affirmed the use of anti-inflammatory therapy to reduce cardiovascular risk; however, the possibility of off-target adverse effects may limit the application. Moreover, systemic inflammatory markers are not sufficiently precise in localizing cardiovascular active inflammation, and conventional cardiovascular imaging methods can only detect structural changes in late-stage disease. Targeted molecular imaging offers imaging-guided precision theragnostic and early upstream preventive approaches by delineating the cellular biological mechanisms underpinning cardiovascular inflammaging and holds the potential to revolutionize the personalized treatment of early atherosclerotic disease. Here, we examine recent developments in molecular imaging in relation to the mechanisms underlying aging-related atherosclerotic cardiovascular disease. We highlight challenges facing the translation of molecular imaging into clinical practice and propose future directions of these novel diagnostic modalities.
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