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干扰素-α与动脉闭塞后侧支循环形成的关系。

The association of interferon-alpha with development of collateral circulation after artery occlusion.

机构信息

Department of Emergency Medicine, The Second Xiangya Hospital, Central South University, Changsha, China.

Department of Cardiovascular Medicine, The Second Xiangya Hospital, Central South University, Changsha, China.

出版信息

Clin Cardiol. 2021 Nov;44(11):1621-1627. doi: 10.1002/clc.23734. Epub 2021 Oct 2.

Abstract

BACKGROUND

Previous studies have demonstrated that interferon (IFN) signaling is enhanced in patients with poor collateral circulation (CC). However, the role and mechanisms of IFN-alpha in the development of CC remain unknown.

METHODS

We studied the serum levels of IFN-alpha and coronary CC in a case-control study using logistics regression, including 114 coronary chronic total occlusion (CTO) patients with good coronary CC and 94 CTO patients with poor coronary CC. Restricted cubic splines was used to flexibly model the association of the levels of IFN-alpha with the incidence of good CC perfusion restoration after systemic treatment with IFN-alpha was assessed in a mice hind-limb ischemia model.

RESULTS

Compared with the first IFN-alpha tertile, the risk of poor CC was higher in the third IFN-alpha tertile (OR: 4.79, 95% CI: 2.22-10.4, p < .001). A cubic spline-smoothing curve showed that the risk of poor CC increased with increasing levels of serum IFN-alpha. IFN-alpha inhibited the development of CC in a hindlimb ischemia model. Arterioles of CC in the IFN-alpha group were smaller in diameter than in the control group.

CONCLUSION

Patients with CTO and with poor CC have higher serum levels of IFN-alpha than CTO patients with good CC. IFN-alpha might impair the development of CC after artery occlusion.

摘要

背景

先前的研究表明,在侧支循环不良(CC)的患者中,干扰素(IFN)信号增强。然而,IFN-α在 CC 发展中的作用和机制尚不清楚。

方法

我们采用逻辑回归,在一项病例对照研究中研究了 IFN-α 血清水平与 CC,纳入了 114 例 CC 良好的冠状动脉慢性完全闭塞(CTO)患者和 94 例 CC 不良的 CTO 患者。使用限制性立方样条灵活地构建了 IFN-α 水平与 IFN-α 全身治疗后良好 CC 灌注恢复发生率的关联模型,在小鼠后肢缺血模型中评估了 IFN-α 全身治疗后良好 CC 灌注恢复的发生率。

结果

与 IFN-α 第一三分位组相比,第三三分位组的 CC 不良风险更高(OR:4.79,95%CI:2.22-10.4,p<0.001)。立方样条平滑曲线显示,CC 不良风险随血清 IFN-α 水平升高而增加。IFN-α 在小鼠后肢缺血模型中抑制 CC 的发展。IFN-α 组 CC 的小动脉直径比对照组小。

结论

与 CC 良好的 CTO 患者相比,CTO 伴 CC 不良的患者血清 IFN-α 水平更高。IFN-α 可能会损害动脉闭塞后的 CC 发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff0c/8571556/d67cc64261e5/CLC-44-1621-g003.jpg

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