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Vitamin D: evidence for an association with coronary collateral circulation development?

机译:维生素D:与冠状动脉侧支循环发展相关的证据?

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Contrary to past beliefs that the human coronary artery system lacks arterial anastomoses, it is now well established that coronary arteries possess a complex network of collateral circulation. Indeed, humans present one of the most developed coronary collateral systems amongst mammals [1]. Coronary collateral vessels originate during embryogenesis by a mechanism known as vasculogenesis, in which local signals promote the migration and differentiation of endothelial progenitor cells, resulting in de novo synthesis of blood vessels. After the embryological stage, development of collaterals relies on two other processes, namely angiogenesis and arteriogenesis. In angiogenesis, new capillaries are formed by sprouting of endothelial cells from pre-existing mature vessels under conditions of ischemia in response to several growth factors, including the vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF). Vascular smooth muscle cells and pericytes also play a role in this process, being particularly important for the stabilization and maturation of new vessels. In contrast, arteriogenesis is defined as a structural remodelling of collaterals pre-formed during embryogenesis, promoted by a redistribution of blood flow and increased shear forces in vessel walls. This is especially observed after coronary total occlusion, when a decrease in pressure distal to the site of obstruction redirects the flow to arteries outside the ischemic area, leading to a positive remodelling of pre-existing arterioles, which can increase up to twelve fold in size [2]. Although functioning collaterals are observed in approximately 20% to 25% of individuals without coronary artery disease (CAD), the degree of coronary obstruction is one of the main determinants of collateralization – individuals with CAD present high prevalence of collaterals. In fact, collateral functionality has been associated with the severity of CAD, as it has been shown that patients with chronic total coronary occlusion have a higher collateral flow index (CFI) than those without chronic occlusion [3]. Therefore, collateral circulation seems to play an important role in salvaging areas of myocardium under ischemia, as exemplified by the observation that well-developed collaterals can limit infarct size [4]. In terms of prognostic value, Seiler et al. [5] evaluated the impact of collateral function, as assessed quantitatively by CFI, on all-cause mortality in a cohort of... View full text...
机译:与过去认为人的冠状动脉系统缺乏动脉吻合的观点相反,现在已经确定冠状动脉具有复杂的侧支循环网络。实际上,人类是哺乳动物中最发达的冠状动脉侧支系统之一[1]。冠状动脉旁支血管通过称为血管生成的机制在胚胎发生过程中起源,其中局部信号促进内皮祖细胞的迁移和分化,从而导致血管从头合成。在胚胎学阶段之后,侧支的发展依赖于另外两个过程,即血管生成和动脉生成。在血管生成中,通过在缺血条件下响应多种生长因子(包括血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF))从已有的成熟血管中萌发内皮细胞而形成新的毛细血管。血管平滑肌细胞和周细胞在此过程中也起作用,对于新血管的稳定和成熟尤为重要。相反,动脉生成被定义为在胚胎生成过程中形成的侧支的结构重塑,其由血流的重新分布和血管壁剪切力的增加而促进。尤其是在冠状动脉完全闭塞后,当阻塞部位远端的压力降低使血流重新导向缺血区域之外的动脉时,会导致先前存在的小动脉发生积极的重塑,其大小可能会增加十二倍[2]。尽管在无冠心病(CAD)的个体中大约有20%至25%的人观察到了功能正常的侧支,但冠状动脉阻塞的程度是侧支化的主要决定因素-具有CAD的个体侧支患病率很高。实际上,侧支功能与CAD的严重程度有关,因为已显示患有慢性总冠状动脉闭塞的患者比没有慢性闭塞的患者具有更高的侧支血流指数(CFI)[3]。因此,侧支循环似乎在缺血下心肌的挽救区域中起着重要作用,正如观察到的那样,发达的侧支会限制梗死面积[4]。就预后价值而言,Seiler等人。 [5]评估了CFI定量评估的侧支功能对一组人群全因死亡率的影响。...查看全文...

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