循环可溶性ST2可预测植入心律转复除颤器的严重心力衰竭患者的全因死亡率。

IF 1.8 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiology Research and Practice Pub Date : 2020-11-17 eCollection Date: 2020-01-01 DOI:10.1155/2020/4375651
Zhi-Wei Hou, Hai-Bo Yu, Yan-Chun Liang, Yang Gao, Guo-Qing Xu, Min Wu, Zhu Mei, Zu-Lu Wang, Zhi-Guo Li, Yu-Ying Li, Hai-Xu Song, Jia-Yin Li, Ya-Ling Han
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引用次数: 1

摘要

背景:心力衰竭(HF)是所有心血管事件的终末期。尽管植入式心律转复除颤器(ICD)治疗降低了高危HF人群的死亡率,但仍有必要确定某些因素是否可以预测心脏装置植入术后的死亡率。生长刺激表达基因2 (ST2)是一种新兴的生物标志物,可用于不同临床环境下HF患者的分层。目的:本研究旨在探讨高危HF植入器械患者血清中基线可溶性ST2 (sST2)水平与临床结局的关系。方法:2017年1月至2018年8月,前瞻性招募LVEF≤35%的心力衰竭患者,连续植入ICD,分析基本特征、基线血清sST2、NT-proBNP水平,随访至少1年。全因死亡率是主要终点。结果:在643天的随访中,150例患者中有16例发生全因死亡(10.67%)。sST2水平高于34.98846 ng/ml的患者全因死亡率显著增高(16.00% vs. 5.33%, P = 0.034)。调整模型(年龄、性别、器械植入、猝死预防、LVEDD、LVEF、WBC和CLBBB、hsTNT、病因学、eGFR)和模型联合NT-proBNP后,每ng/ml sST2的全因死亡风险分别增加2.5%和1.9%。预测全因死亡的最佳sST2截止值为43.42671 ng/ml(曲线下面积:0.72,敏感性:0.69,特异性:0.69)。与sST2水平低于43.42671 ng/ml的患者相比,高于阈值的患者全因死亡风险更高(5.1%比21.2%,P = 0.002)。ST2水平≥43.42671 ng/ml是全因死亡率的独立预测因子(HR: 3.30 [95% CI 1.02-10.67])。年龄(HR: 1.06 [95% CI: 1.01-1.12])和NT-proBNP / 100增加(HR: 1.02 [95% CI: 1.01-1.03])也与ICD患者的全因死亡率相关。结论:sST2水平与全因死亡风险相关,43.43 ng/ml阈值对预测重度心力衰竭患者全因死亡率有较好的区分作用,推荐用于ICD植入。因此,即使在ICD植入后,sST2水平仍高于43.42671 ng/ml的患者也应密切监测。
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Circulating Soluble ST2 Predicts All-Cause Mortality in Severe Heart Failure Patients with an Implantable Cardioverter Defibrillator.

Background: Heart failure (HF) is the terminal stage of all cardiovascular events. Although implantable cardioverter defibrillator (ICD) therapies have reduced mortality among the high-risk HF population, it is necessary to determine whether certain factors can predict mortality even after cardiac device implantation. Growth stimulation expressed gene 2 (ST2) is an emerging biomarker for HF patient stratification in different clinical settings.

Aims: This study aimed to investigate the relationship between baseline soluble ST2 (sST2) levels in serum and the clinical outcomes of high-risk HF patients with device implantation.

Methods: Between January 2017 and August 2018, we prospectively recruited consecutive patients implanted with an ICD for heart failure, with LVEF ≤35% as recommended, and analyzed the basic characteristics, baseline serum sST2, and NT-proBNP levels, with at least 1-year follow-up. All-cause mortality was the primary endpoint.

Results: During a 643-day follow-up, all-cause mortality occurred in 16 of 150 patients (10.67%). Incidence of all-cause mortality increased significantly in patients with sST2 levels above 34.98846 ng/ml (16.00% vs. 5.33%, P = 0.034). After adjusting the model (age, gender, device implantation, prevention of sudden death, LVEDD, LVEF, WBC and CLBBB, hsTNT, etiology, and eGFR) and the model combined with NT-proBNP, the risk of all-cause death was increased by 2.5% and 1.9%, respectively, per ng/ml of sST2. The best sST2 cutoff for predicting all-cause death was 43.42671 ng/ml (area under the curve: 0.72, sensitive: 0.69, and specificity: 0.69). Compared to patients with sST2 levels below 43.42671 ng/ml, the risk of all-cause mortality was higher in those with values above the threshold (5.1% vs. 21.2%, P = 0.002). ST2 level ≥43.42671 ng/ml was an independent predictor of all-cause mortality (HR: 3.30 [95% CI 1.02-10.67]). Age (HR: 1.06 [95% CI: 1.01-1.12]) and increased NT-proBNP per 100 (HR: 1.02 [95% CI: 1.01-1.03]) were also associated with all-cause mortality in ICD patients.

Conclusions: sST2 level was associated with risk of all-cause mortality, and a threshold of 43.43 ng/ml showed good distinguishing performance to predict all-cause mortality in patients with severe heart failure, recommended for ICD implantation. Patients with sST2 levels more than 43.42671 ng/ml even after ICD implantation should therefore be monitored carefully.

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来源期刊
Cardiology Research and Practice
Cardiology Research and Practice Medicine-Cardiology and Cardiovascular Medicine
CiteScore
4.40
自引率
0.00%
发文量
64
审稿时长
13 weeks
期刊介绍: Cardiology Research and Practice is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies that focus on the diagnosis and treatment of cardiovascular disease. The journal welcomes submissions related to systemic hypertension, arrhythmia, congestive heart failure, valvular heart disease, vascular disease, congenital heart disease, and cardiomyopathy.
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