女性非阻塞性冠状动脉疾病:当前证据和未来方向

Leanna R Smith, Moro O Salifu, Isabel M McFarlane
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引用次数: 7

摘要

背景:超过一半患有心绞痛的女性发现冠状动脉造影评估呈阴性。在这些患者中,高达50%被诊断为冠状动脉微血管功能障碍(CMD),这是指冠状动脉循环小血管的病理改变。CMD病理生理学的特点是,由于多种条件和危险因素而发生的内皮损伤是CMD发生和发展的刺激事件。CMD导致心肌需求和灌注不匹配,导致在主要血管没有梗阻性病变的情况下出现心脏缺血的体征和症状。CMD可以通过多种侵入性方法诊断,这些方法允许对微血管进行更具体的评估,也可以通过非侵入性成像技术诊断,如心脏正电子发射断层扫描(PET)和磁共振成像(MRI)。CMD的危险因素与阻塞性冠状动脉疾病(CAD)的危险因素有显著重叠——高血压、高胆固醇血症和糖尿病仍然是显著的预测因素。然而,这些情况只占女性CMD病例的20%。研究结果:女性有性别特异性的危险因素,如更年期、妊娠、多囊卵巢综合征(PCOS),以及慢性炎症性疾病的更高倾向。雌激素通过增加一氧化氮的产生而具有心脏保护作用,一氧化氮是内皮细胞释放的一种有效的血管扩张剂。因此,更年期的荷尔蒙变化可能加速内皮损伤,进而加速CMD。目前的治疗侧重于解决心血管疾病的危险因素,如降压药、减肥和血糖控制。结论:考虑到女性CMD的多因素性质,以及心脏病的广泛非典型危险因素,需要一种更细致的方法来解决CMD的各种病理生理。
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Non-Obstructive Coronary Artery Disease in Women: Current Evidence and Future Directions.

Background: Over half of women who present with angina are found to have negative coronary angiographic assessments. Of these patients, up to 50% are diagnosed with coronary microvascular dysfunction (CMD), which refers to pathologic changes within the small vessels of the coronary circulation. The hallmark of the pathophysiology of CMD is that endothelial damage, which occurs due to a multitude of conditions and risk factors, is the inciting event for the development and progression of CMD. CMD leads to a mismatch in myocardial demand and perfusion, leading to signs and symptoms of cardiac ischemia in the absence of obstructive lesions in the major vessels. CMD can be diagnosed through a variety of both invasive methods that allow a more specific evaluation of the microvasculature and non-invasive imaging techniques, such as cardiac positron emission tomography (PET) and magnetic resonance imaging (MRI). Risk factors for CMD overlap significantly with those of obstructive coronary artery disease (CAD) - hypertension, hypercholesterolemia, and diabetes remain salient predictors. However, these conditions only account for 20% of CMD cases in females.

Findings: Women have sex-specific risk factors such as menopause, pregnancy, polycystic ovarian syndrome (PCOS), and a higher proclivity toward chronic inflammatory disorders. Estrogen has a cardioprotective effect by increasing production of nitric oxide, a potent vasodilator released by endothelial cells. As a result, the hormonal changes of menopause may accelerate endothelial damage, and in turn, CMD. Current treatments focus on addressing the risk factors of cardiovascular disease, such as anti-hypertensive drugs, weight loss, and glucose control.

Conclusion: Given the multifactorial nature of CMD in women, and the extensive atypical risk factors for cardiac disease, a more nuanced approach is needed that addresses the varied pathophysiology of CMD.

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