蛋白质组学鉴定心脏骤停后脑损伤的发病机制和监测和早期预测的新生物标志物:一项随机动物研究

IF 2.1 Q3 CRITICAL CARE MEDICINE
Zhun Yao , Yuanrui Zhao , Liping Lu , Song Xu , Yinping Li , Zhui Yu
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引用次数: 0

摘要

目的心脏骤停后脑损伤(PCABI)是复苏后死亡和残疾的主要原因。本研究旨在探讨PCABI的发病机制和监测其进展和早期预后的新生物标志物。方法采用高钾血症诱导小鼠PCABI停搏并成功复苏模型。年轻成年雄性C57BL/6小鼠随机分为假手术组和心脏停止/复苏组。以假手术小鼠为对照。复苏后24 h行神经学检查,分为对照组(n = 4)、重度PCABI组(n = 3)、轻度PCABI组(n = 3)。收集大脑皮层进行数据独立获取-蛋白质组学分析。通过三个亚组的两两比较和随后的生物信息学分析,确定了发病机制和潜在的生物标志物。从ttm试验的第二次分析中提取的人类血清蛋白质组图谱用于联合分析,以确定同一时间点的共同和临床相关的生物标志物。通过实验和外部验证来验证新型生物标志物与PCABI神经死亡之间的关联。结果蛋白质组学分析鉴定并定量了7745个蛋白。在PCABI的进展过程中,最突出的蛋白质组学变化与外部刺激反应、应激反应、生物和代谢过程的调节、膜系统和炎症反应有关。通过对三组患者进行两两比较,确定了10个潜在的生物标志物,在复苏后24小时的人体研究中,脂脂素-2和血管紧张素原是常见的生物标志物。实验证实脂钙素-2与PCABI的神经变性密切相关。结论应激、炎症和代谢反应在PCABI的发展中起重要作用。Lipocalin-2是一种用于复苏后24小时监测和早期神经预后的新型生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomics identify pathogenesis and novel biomarkers for monitoring and early prognostication of brain injury after cardiac arrest: a randomized animal study

Aim

Post-cardiac arrest brain injury (PCABI) is the leading cause of death and disability after resuscitation. This study aimed to investigate the pathogenesis and novel biomarkers for monitoring the progression and early prognostication of PCABI.

Methods

Mouse model of PCABI was induced by hyperkalemia-induced asystole and successful resuscitation. Young adult male C57BL/6 mice were randomized into sham-operation or asystole/resuscitation. The sham-operated mice were selected as control. Neurological examinations were performed at 24 h after resuscitation, and three groups were set: control (n = 4), severe PCABI (n = 3), and mild PCABI (n = 3). Cerebral cortexes were collected for data-independent acquisition-proteomic analyses. The pathogenesis and potential biomarkers were identified through the pairwise comparisons of three subgroups and subsequent bioinformatics analyses. Human serum proteomes profiles, extracted from a published work of the second analysis of TTM-trial, were used for joint analyses to identify the common and clinically relevant biomarkers at the same timepoint. Experimental and external validation were performed to verify the association between novel biomarkers and neural death in PCABI.

Results

The proteomic analysis identified and quantified 7,745 proteins. The most prominent proteomic changes were related to response to external stimulus, stress response, regulation of biological and metabolic process, endomembrane system, and inflammatory response in the PCABI progression. 10 potential biomarkers were identified by the pairwise comparisons of three groups, and lipocalin-2 and angiotensinogen are common biomarkers with human studies at 24 h after resuscitation. Experimental validation verified that lipocalin-2 was closely associated with neurodegeneration in PCABI.

Conclusions

Stress, inflammatory, and metabolic responses play important roles in the progression of PCABI. Lipocalin-2 is a novel biomarker for monitoring and early neuroprognostication at 24 h after resuscitation.
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来源期刊
Resuscitation plus
Resuscitation plus Critical Care and Intensive Care Medicine, Emergency Medicine
CiteScore
3.00
自引率
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审稿时长
52 days
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