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基于蛋白质表达鉴定患者亚型以预测心肌梗死后心力衰竭

Identification of patient subtypes based on protein expression for prediction of heart failure after myocardial infarction.

作者信息

Heyse Wilfried, Vandewalle Vincent, Marot Guillemette, Amouyel Philippe, Bauters Christophe, Pinet Florence

机构信息

UniversityLille, Inserm, CHU Lille, Institut Pasteur de Lille, U1167 - RID-AGE - Facteurs de risque et déterminants moléculaires des maladies liées au vieillissement, 59000 Lille, France.

Inria, Modal, 59000 Lille, France.

出版信息

iScience. 2023 Feb 11;26(3):106171. doi: 10.1016/j.isci.2023.106171. eCollection 2023 Mar 17.

Abstract

This study investigates the ability of high-throughput aptamer-based platform to identify circulating biomarkers able to predict occurrence of heart failure (HF), in blood samples collected during hospitalization of patients suffering from a first myocardial infarction (MI). REVE-1 (derivation) and REVE-2 (validation) cohorts included respectively 254 and 238 patients, followed up respectively 9 · 2 ± 4 · 8 and 7 · 6 ± 3 · 0 years. A blood sample collected during hospitalization was used for quantifying 4,668 proteins. Fifty proteins were significantly associated with long-term occurrence of HF with all-cause death as the competing event. -means, an unsupervised clustering method, identified two groups of patients based on expression levels of the 50 proteins. Group 2 was significantly associated with a higher risk of HF in both cohorts. These results showed that a subset of 50 selected proteins quantified during hospitalization of MI patients is able to stratify and predict the long-term occurrence of HF.

摘要

本研究调查了基于高通量适体的平台识别循环生物标志物的能力,这些生物标志物能够在首次心肌梗死(MI)患者住院期间采集的血液样本中预测心力衰竭(HF)的发生。REVE-1(衍生)队列和REVE-2(验证)队列分别包括254例和238例患者,随访时间分别为9.2±4.8年和7.6±3.0年。住院期间采集的血液样本用于定量4668种蛋白质。50种蛋白质与以全因死亡为竞争事件的HF长期发生显著相关。-均值是一种无监督聚类方法,根据这50种蛋白质的表达水平将患者分为两组。在两个队列中,第2组与更高的HF风险显著相关。这些结果表明,在MI患者住院期间定量的50种选定蛋白质的一个子集能够分层并预测HF的长期发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7d3/10006628/d82a52b9cbf5/fx1.jpg

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