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Elabela 作为一种新型标志物:与下肢动脉疾病患者的 WIfI 截肢风险评分密切相关。

Elabela as a novel marker: Well-correlated with WIfI amputation risk score in lower extremity arterial disease patients.

机构信息

Department of Cardiology, Faculty of Medicine, Gaziantep University; Gaziantep-Turkey.

Department of Cardiology, Adana City Training and Research Hospital; Adana-Turkey.

出版信息

Anatol J Cardiol. 2021 May;25(5):330-337. doi: 10.14744/AnatolJCardiol.2020.17329.

Abstract

OBJECTIVE

Worldwide, over 200 million people are diagnosed with lower extremity arterial disease (LEAD). LEAD significantly increases the risk of death and amputation of the lower limb. A new classification system (WIfI) has been proposed to initially assess all patients with ischemic rest pain or wounds and also predicts 1-year amputation risk. Elabela is a bioactive peptide and a part of the apelinergic system, which has beneficial effects on body fluid homeostasis and cardiovascular health. We aimed to investigate serum Elabela levels in LEAD.

METHODS

A total of 119 subjects were enrolled in this cross-sectional study, 60 of whom were in the LEAD group and 59 in the control group. All participants underwent physical examination and routine biochemical tests, including serum Elabela levels. Additionally, the LEAD group was divided into subgroups according to the Rutherford classification, ankle-brachial index (ABI) values, and WIfI risk scores.

RESULTS

Serum low-density lipoprotein, Elabela, and high-sensitivity C-reactive protein (Hs-CRP) levels were statistically higher in the LEAD group (p=0.002, p<0.001, and p<0.001, respectively). In the Rutherford classification, as the stage increased, Elabela and Hs-CRP levels increased similarly (p<0.001). Elabela levels were statistically found to be positively correlated with Hs-CRP and WIfI amputation score but negatively correlated with ABI (p<0.001).

CONCLUSION

Serum Elabela level, which is known to be increased in inflammatory processes, has the potential in predicting low extremity arterial obstruction and WIfI amputation risk in LEAD patients.

摘要

目的

全球有超过 2 亿人被诊断患有下肢动脉疾病(LEAD)。LEAD 显著增加了下肢死亡和截肢的风险。已经提出了一种新的分类系统(WIfI),用于初步评估所有患有缺血性静息痛或伤口的患者,并预测 1 年内的截肢风险。Elabela 是一种生物活性肽,是阿片肽能系统的一部分,对体液平衡和心血管健康有有益影响。我们旨在研究 LEAD 患者的血清 Elabela 水平。

方法

这项横断面研究共纳入了 119 名受试者,其中 60 名在 LEAD 组,59 名在对照组。所有参与者都接受了体格检查和常规生化检查,包括血清 Elabela 水平。此外,LEAD 组根据 Rutherford 分类、踝肱指数(ABI)值和 WIfI 风险评分进行了分组。

结果

LEAD 组的血清低密度脂蛋白、Elabela 和高敏 C 反应蛋白(Hs-CRP)水平均显著升高(p=0.002、p<0.001 和 p<0.001)。在 Rutherford 分类中,随着疾病阶段的增加,Elabela 和 Hs-CRP 水平也呈相似升高(p<0.001)。Elabela 水平与 Hs-CRP 和 WIfI 截肢评分呈正相关,与 ABI 呈负相关(p<0.001)。

结论

已知在炎症过程中升高的血清 Elabela 水平可能有助于预测 LEAD 患者下肢动脉阻塞和 WIfI 截肢风险。

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